Pharma company: sandoz
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List of sandoz products:
- 4D
- ACC
- ACC Eco
- ACC Long
- APO-Go Pen
- ASS
- Accutin - Pharmacological action Accutin is a pharmaceutical agent for the treatment of acne. Contributes to the normalization of terminal cell differentiation, inhibits the hyperproliferation of the epithelium of excretory ducts of the sebaceous glands, the formation of detritus and makes it easier to evacuate. Due to this reduced production of sebum and facilitates its isolation, normal structure, decreasing the inflammatory reaction around the glands. For external and systemic application...
- Acebutolol - A cardioselective beta-adrenergic antagonist with little effect on the bronchial receptors. The drug has stabilizing and quinidine-like effects on cardiac rhythm as well as weak inherent sympathomimetic action. [PubChem] Indication: For the management of hypertension and ventricular premature beats in adults. Acebutolol is a cardioselective, beta-adrenoreceptor blocking agent, which possesses mild intrinsic sympathomimetic activity (ISA) in its therapeutically effective dose range. In general,...
- Aceclofenac
- Acenocoumarol - Acenocoumarol is a coumarin derivative used as an anticoagulant. Coumarin derivatives inhibit the reduction of vitamin K by vitamin K reductase. This prevents carboxylation of vitamin K-dependent clotting factors, II, VII, XI and X, and interferes with coagulation. Hematocrit, hemoglobin, international normalized ratio and liver panel should be monitored. Patients on acenocoumarol are prohibited from giving blood. Indication: For the treatment and prevention of thromboembolic diseases. More...
- Acenorm
- Acenorm HCT
- Acetaminophen; Codeine - This combination medication is used to help relieve mild to moderate pain. It contains a narcotic pain reliever (codeine) and a non-narcotic pain reliever (acetaminophen). Codeine works in the brain to change how your body feels and responds to pain. Acetaminophen can also reduce a fever. OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a...
- Acetate de Cyproterone
- Acetazolamide - DESCRIPTION Acetazolamide, an inhibitor of the enzyme carbonic anhydrase, is a white to faintly yellowish white crystalline, odorless powder, weakly acidic, very slightly soluble in water and slightly soluble in alcohol. The chemical name for acetazolamide is N -(5-Sulfamoyl-1,3,4-thiadiazol-2yl)-acetamide and has the following structural formula: Acetazolamide is available for...
- Aceterin
- Aceterin Express
- Acetilcisteina
- Acetylcysteine - 1 INDICATIONS AND USAGE CETYLEV is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (RSI). CETYLEV is an antidote for acetaminophen overdose indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of...
- Acetylsalicylzuur Sandoz Cardio - Pharmacological action Acetylsalicylzuur Sandoz Cardio is a NSAIDs. It has anti-inflammatory, analgesic and antipyretic effect, and inhibits platelet aggregation. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid which is a precursor of prostaglandins which play a major role in the pathogenesis of inflammation, pain and fever. Reduction of prostaglandins (mainly E1) in the thermoregulation center leads to a decrease in...
- Acetylsalicylzuur Sandoz Neuro - Pharmacological action Acetylsalicylzuur Sandoz Neuro is a NSAIDs. It has anti-inflammatory, analgesic and antipyretic effect, and inhibits platelet aggregation. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid which is a precursor of prostaglandins which play a major role in the pathogenesis of inflammation, pain and fever. Reduction of prostaglandins (mainly E1) in the thermoregulation center leads to a decrease in...
- Acic Creme - Pharmacological action Acic Creme is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against Herpes...
- Aciclovir - Pharmacological action Aciclovir is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against Herpes...
- Aciclovir-BC - Pharmacological action Aciclovir-BC is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against Herpes...
- Acinil
- Aclinda
- Acnocin
- Acti-B12 - Pharmacological action Vitamin B12 refers to a group of water-soluble vitamins. It has high biological activity. Acti-B12 is necessary for normal hematopoiesis (promotes maturation of erythrocytes). Involved in the processes of transmethylation, hydrogen transport, synthesis of methionine, nucleic acids, choline, creatine. Contributes to the accumulation in erythrocytes of compounds containing sulfhydryl groups. Has a beneficial effect on liver function and the nervous system. Activates...
- Actimax - Actimax information Actimax is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Actimax indications Actimax is usually prescribed by doctors and personal health care providers to patients who are suffering from bacterial infections of the ears, throat, chest, urinary tract and to the individuals who have been diagnosed with the presence of a mild form of gonorrhea. Actimax may also be recommended...
- Actobim
- Acylanide
- Adana - Adana information Adana is a drug that classified as an Angiotensin II receptor antagonist. Adana indications This blood pressure medication (Adana) is indicated for the treatment of hypertension or high blood pressure. Adana works by preventing the narrowing of blood vessels and arteries and it also prevents the constriction of the flow of blood. Buy Adana, as it is also prescribed for the treatment of kidney disease caused by diabetes. Adana warnings Adana may not be fully...
- Adana Plus
- Adelphane-Esidrex
- Aeropax
- Agyr - Pharmacological action Agyr is a broad-spectrum antimicrobial drug of fluoroquinolone group with bactericidal action. Inhibits DNA gyrase and inhibits the synthesis of bacterial DNA. Highly active against most gram-negative bacteria: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae. Agyr is active against Staphylococcus spp. (including strains producing and not producing penicillinase,...
- Ainelac - Pharmacological action Ainelac is a NSAID, derivative of pyrrolizine-carboxylic acid. This medication has a marked analgesic effect, also has anti-inflammatory and mild antipyretic action. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Pharmacokinetics After oral administration Ainelac is absorbed from the...
- Ainex - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ak Tate - Pharmacological action Ak Tate is a glucocorticosteroid (GCS). This medication inhibits the function of leukocytes and tissue macrophages. Prednisolone restricts the migration of leukocytes in the area of inflammation. This drug violates the ability of macrophages to phagocytosis and the formation of interleukin-1. Ak Tate contributes to the stabilization of lysosomal membranes, thereby reducing the concentration of proteolytic enzymes in inflammation. This medicine decreases capillary...
- Aknereduct - Aknereduct information Aknereduct belongs to the group tetracycline, which is used to treat infections caused by bacteria. Aknereduct works by interfering with the ability of the bacteria to produce proteins, which is very essential to the growth and increase of numbers to the bacteria. Aknereduct stops the spread of infection and the remaining bacteria are killed by the immune system or eventually die. Aknereduct indications Aknereduct is indicated for the treatment different...
- Albuterol - Pharmacological action Albuterol Pharmaceuticals is a beta adrenoagonists with a predominant effect on beta2-adrenergic receptors (localized, particularly in the bronchi, myometrium, blood vessels). This medication prevents and reduces or eliminates bronchospasm, reduces the resistance in the airways, increases the vital capacity. It prevents the release of histamine, slow reacting substance from mast cells and factors chemotaxis of neutrophils. Compared with other drugs of this group has...
- Albuterol; Ipratropium
- Alcohol dehydrated
- Alendronate - Alendronate is a nitrogen-containing, second generation bisphosphonate. Bisphosphonates were first used to treat Paget’s disease in 1971. This class of medications is comprised of inorganic pyrophosphate analogues that contain non-hydrolyzable P-C-P bonds. Similar to other bisphosphonates, alendronate has a high affinity for bone mineral and is taken up during osteoclast resorption. Alendronate inhibits farnesyl pyrophosphate synthetase, one of the enzymes in the mevalonic acid pathway...
- Alexan
- Alfentanil - A short-acting opioid anesthetic and analgesic derivative of fentanyl. It produces an early peak analgesic effect and fast recovery of consciousness. Alfentanil is effective as an anesthetic during surgery, for supplementation of analgesia during surgical procedures, and as an analgesic for critically ill patients. [PubChem] Indication: For the management of postoperative pain and the maintenance of general anesthesia. Alfentanil is a synthetic opioid analgesic. Alfentanil interacts...
- Alfuzosin - Alfuzosin (INN, provided as the hydrochloride salt) is an alpha-adrenergic blocker used to treat benign prostatic hyperplasia (BPH). It works by relaxing the muscles in the prostate and bladder neck, making it easier to urinate. [Wikipedia] Indication: For the reduction of urinary obstruction and relief of associated manifestations (eg. sensation of incomplete bladder emptying or straining, urgency, interrupted or weak stream) in patients with symptomatic beningn prostatic hyperplasia....
- Alfuzosine
- Alfuzosine L.P.
- Alfuzosine Retard
- Alginate de Sodium; Bicarbonate de Sodium
- Allopur - Pharmacological action Allopur is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney. Allopurinol increases...
- Allopurinol - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Allopurinol-BC - Pharmacological action Allopurinol-BC is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney. Allopurinol...
- Allotyrol - Pharmacological action Allotyrol is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney. Allopurinol increases...
- Alnok
- Alprazolam - Pharmacological action Alprazolam is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor activating...
- Alprazolam ER - Pharmacological action Alprazolam ER is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor activating...
- Altavera
- Alucol
- Amanta - Pharmacological action Amanta is an antiparkinsonian and antiviral drug, a tricyclic symmetric adamantanamin. This medication blocks glutamate NMDA-receptors, thus reducing the excessive stimulatory effect of cortical glutamate neurons in the neostriatum that develops against the backdrop of lack of dopamine. Amantadine inhibits NMDA-receptors in the neurons of the substantia nigra reduces the intake of these Ca2+, which reduces the possibility of destruction of these neurons. In a...
- Amantadine - Pharmacological action Amantadine is an antiparkinsonian and antiviral drug, a tricyclic symmetric adamantanamin. This medication blocks glutamate NMDA-receptors, thus reducing the excessive stimulatory effect of cortical glutamate neurons in the neostriatum that develops against the backdrop of lack of dopamine. Amantadine inhibits NMDA-receptors in the neurons of the substantia nigra reduces the intake of these Ca2+, which reduces the possibility of destruction of these neurons. In a...
- Ambesyl
- Amdixal
- Amicosol
- Amikacin - Amikacin is a semi-synthetic aminoglycoside antibiotic derived from kanamycin A. Similar to other aminoglycosides, amikacin disrupts bacterial protein synthesis by binding to the 30S ribosome of susceptible organisms. Binding interferes with mRNA binding and tRNA acceptor sites leading to the production of non-functional or toxic peptides. Other mechanisms not fully understood may confer the bactericidal effects of amikacin. Amikacin is also nephrotoxic and ototoxic. Indication: For short-term...
- Amilorid HCT
- Amiloride HCT
- Amiloride; Hydrochlorothiazide - This product is used to treat high blood pressure ( hypertension ), heart failure , or extra fluid in the body ( edema ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: amiloride and hydrochlorothiazide . Both medications are "water pills" (diuretics) and cause your body to get rid of extra salt and water. This effect may increase the amount of urine you make when you first start the product. Amiloride...
- Aminophylline - SPL UNCLASSIFIED SECTION Aminophylline Injection, USP 25 mg/mL Aminophylline, Dihydrate (Equivalent to 19.7 mg/mL of Anhydrous Theophylline) ...
- Amio
- Amiodar
- Amiodar Mite
- Amiodaron
- Amiodarone - An antianginal and antiarrhythmic drug. It increases the duration of ventricular and atrial muscle action by inhibiting Na,K-activated myocardial adenosine triphosphatase. There is a resulting decrease in heart rate and in vascular resistance. [PubChem] Indication: Intravenously, for initiation of treatment and prophylaxis of frequently recurring ventricular fibrillation and hemodynamically unstable ventricular tachycardia in patients refractory to other therapy. Orally, for the treatment of...
- Amisulpride - Amisulpride (trade name Solian) is an antipsychotic drug sold by Sanofi-Aventis. It is not approved for use in the United States, but is approved for use in Europe and Australia for the treatment of psychoses and schizophrenia. Additionally, it is approved in Italy for the treatment of dysthymia (under the brand name Deniban). Amisulpride is a selective dopamine antagonist. Indication: Investigated for use/treatment in schizophrenia and schizoaffective disorders, mania in bipolar disorder, and...
- Amitriptyline - Pharmacological action Amitriptyline is an antidepressant tricyclic group of compounds derived dibenzocycloheptadiene. The mechanism of antidepressant action is associated with an increased concentration of norepinephrine in the synapses and / or serotonin in the central nervous system depression due to reverse neuronal capture of these mediators. When anxiety and depressive states this medication reduces anxiety, agitation and depressive symptoms. Also this drug has some analgesic...
- Amizide
- Amlibon
- Amlibon B
- Amlidual
- Amlipril
- Amlo Eco
- Amlodipin
- Amlodipin Sandoz Eco
- Amlodipine - Amlodipine is a long-acting 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, amlodipine prevents calcium-dependent myocyte contraction and vasoconstriction. A second proposed mechanism for the drug’s vasodilatory effects involves pH-dependent inhibition of calcium influx via inhibition of smooth...
- Amlodipine; Benazepril - This medication is a combination of two drugs: a calcium channel blocker ( amlodipine ) and an ACE inhibitor ( benazepril ). It is used to treat high blood pressure ( hypertension ). It works by relaxing blood vessels so that blood can flow more easily. Lowering high blood pressure helps prevent strokes, heart attacks and kidney problems.
- Amlodipinemaleaat
- Amlopin
- Amoksiklav
- Amoksiklav Forte
- Amoksiklav Quick Tabs
- Amoksiklav Quicktabs
- Amoxapine - Suicidality and Antidepressant Drugs Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of amoxapine or any other antidepressant in a child, adolescent, or young adult must balance this risk...
- Amoxclav
- Amoxi
- Amoxicilina
- Amoxicilina; Acido Clavulanico
- Amoxicillin - 1.1 Infections of the Ear, Nose, and Throat Amoxicillin tablets are indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) isolates of Streptococcus species. (α- and β-hemolytic isolates only), Streptococcus pneumoniae, Staphylococcus spp., or Haemophilus influenzae. 1.2 Infections of the Genitourinary Tract Amoxicillin tablets are indicated in the treatment of infections due to susceptible (ONLY...
- Amoxicillin Bid
- Amoxicillin Comp
- Amoxicillin; Clavulanate
- Amoxicilline - Pharmacological action Amoxicillin is an antibiotic of group semisynthetic penicillins a wide spectrum of action. It is a 4-hydroxyl analog of ampicillin. It has bactericidal action. amoxicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (except strains producing penicillinase), Streptococcus spp; aerobic gram-negative bacteria: Neisseria Gonorrhoeae, Neisseria Meningitidis, Escherichia Coli, Shigella spp., Salmonella spp., Klebsiella spp. Microorganisms...
- Amoxicilline Viaref
- Amoxicilline; Acide Clavulanique
- Amoxicilline; Acide Clavulanique Adultes
- Amoxicilline; Acide Clavulanique Enfants
- Amoxicilline; Acide Clavulanique Nourrissons
- Amoxicilline; Clavulaanzuur
- Amoxiclav
- Amoxillat
- Amoxillat-Clav
- Amoxycillin-BC
- Amphetamine Combo
- Ampi-Rol
- Ampicillat
- Ampicillin - DESCRIPTION: Ampicillin for injectable suspension, veterinary is a broad-spectrum penicillin which has bactericidal activity against a wide range of common gram-positive and gram-negative bacteria. Each 25 g vial contains: 25 g ampicillin activity as ampicillin trihydrate, 90 mg methylparaben (as preservative), 10 mg propylparaben (as preservative), 200 mg lecithin, 500 mg povidone, 200 mg sodium chloride, 600 mg sodium...
- Ampicillin; Sulbactam
- Amycycline
- Anagrelide - Anagrelide is a drug used for the treatment of essential thrombocytosis (ET; essential thrombocythemia). It also has been used in the treatment of chronic myeloid leukemia. [Wikipedia] Indication: For the treatment of patients with thrombocythemia, secondary to myeloproliferative disorders, to reduce the elevated platelet count and the risk of thrombosis and to ameliorate associated symptoms including thrombo-hemorrhagic events. Anagrelide is a drug used for the treatment of essential...
- Analgesic / Calmative
- Anastraze
- Anastrozole - 1 INDICATIONS AND USAGE Anastrozole is an aromatase inhibitor indicated for: Adjuvant treatment of postmenopausal women with hormone receptor-positive early breast cancer ( 1.1 ) First-line treatment of postmenopausal women with hormone receptor-positive or hormone receptor unknown locally advanced or metastatic breast cancer ( ...
- Ancasal
- Ancatropine Gel
- Ancatropine Gel Plain
- Ancatropine Infant Drops
- Anectine
- Anlos
- Anoclor
- Antagel - This medication is used to treat the symptoms of too much stomach acid such as stomach upset, heartburn , and acid indigestion. It is also used to relieve symptoms of extra gas such as belching, bloating , and feelings of pressure/discomfort in the stomach/gut. Simethicone helps break up gas bubbles in the gut. Aluminum and magnesium antacids work quickly to lower the acid in the stomach. Liquid antacids usually work faster/better than tablets or capsules. This medication works only...
- Anthex - Pharmacological action Mebendazole is a worming medication a broad spectrum of action, it is most effective when enterobioze. This drug causes irreversible disturbance of glucose utilization in the body of the worm and inhibits the synthesis of ATP. Pharmacokinetics Mebendazole is practically not absorbed from the gastrointestinal tract. The plasma protein binding is 90%. This medication is distributed unevenly in organs and accumulates in adipose tissue, liver, and larvae of helminths...
- Antiflam - Pharmacological action NSAIDs, a derivative of phenylacetic acid, diclofenac has a pronounced anti-inflammatory, analgesic and mild antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to two mechanisms: peripheral (indirectly, through suppression of prostaglandin...
- Antimet - Pharmacological action Cinnarizine is a calcium channel blocker class IV with a predominant effect on the brain vessels, a derivative of piperazine. This medication improves cerebral, coronary and peripheral circulation. Cinnarizine violates the entrance of calcium ions into vascular smooth muscle cells. This drug lowers the tone of arteriolar smooth muscle, decreases the vasoconstrictor response to biogenic substances (epinephrine, norepinephrine, bradykinin). Cinnarizine reduces the...
- Antipres - Pharmacological action Sertraline (with the generic name of Sertraline) belongs to the groups of drugs known as selective serotonin reuptake inhibitors. These selective serotonin reuptake drugs influence chemical imbalance in the brain responsible for depression, panic anxiety, obsessive compulsive disorder and others. Why is Sertraline prescribed? Sertraline is indicated for the treatment of: depression panic anxiety disorders obsessive compulsive disorder PSTD or post traumatic...
- Antrenyl
- Antrenyl Duplex
- Anuzinc
- Anuzinc HC
- Anuzinc HC Plus
- Anzem
- Apresolina
- Aquareduct - Pharmacological action Spironolactone is a potassium, magnesium sparing diuretic. This medication is a competitive antagonist of aldosterone on the effect on distal nephron (competes for binding sites on cytoplasmic protein receptors, reduces the synthesis of permeases in the aldosterone-sensitive part of collecting tubules and distal tubules), increases the excretion of Na+, Cl- and water and reduces the excretion of K+ and urea, reduces the titratable acidity of urine. Increased diuresis...
- Aquaretic
- Argatroban in Dextrose
- Argatroban in Sodium Chloride
- Aristocort - Triamcinolone belongs to the class of medications called topical corticosteroids . It is used to treat certain skin conditions, including psoriasis and allergic eczema. It may also be used to relieve itchiness. It works by reducing inflammation or swelling of the skin. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If...
- Aristocort Forte
- Aristospan
- Arthrisin
- Arthroforte
- Articulen
- Artonil
- Artria
- Asbron
- Aspireff
- Aspirin - Active ingredient (in each tablet) Buffered aspirin equal to 81 mg aspirin (NSAID)* (buffered with calcium carbonate, magnesium carbonate and magnesium oxide) *nonsteroidal anti-inflammatory drug Purpose Pain reliever Uses temporarily relieves minor...
- Astaz-P
- Asthmoprotect
- Asthmoprotect Retard
- Atedurex
- Atedurex Mite
- Atehexal - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenil - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenil Mite - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenil Submite - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenolol - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenolol Comp.
- Atenolol; Chloortalidon
- Atenor - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenotyrol - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atenotyrol Comp.
- Ateren
- Aterol - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Atomoxetine - Pharmacological action Atomoxetine is a centrally acting sympathomimetic. This medication is highly selective potent inhibitor of presynaptic norepinephrine transporters. Atomoxetine has minimal affinity to the other noradrenergic receptors or to other transporters or receptors of neurotransmitters. This drug does not apply to psychostimulants and it is not a derivative of amphetamine. In clinical trials there were not noted of increase symptoms or any adverse events associated with...
- Atorsan
- Atorvastatin - Pharmacological action Atorvastatin is a lipid-lowering drugs of the statin group. An inhibition of HMG-CoA reductase leads to a series of sequential reactions that result in reduced intracellular cholesterol content and it is a compensatory increase in activity of LDL receptors and thus accelerate the catabolism of LDL cholesterol. The lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. The reduction in LDL cholesterol is dose-dependent and is...
- Atracurium - A non-depolarizing neuromuscular blocking agent with short duration of action. Its lack of significant cardiovascular effects and its lack of dependence on good kidney function for elimination provide clinical advantage over alternate non-depolarizing neuromuscular blocking agents. [PubChem] Indication: For use, as an adjunct to general anesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. Atracurium is a...
- Atropine - An alkaloid, originally from Atropa belladonna, but found in other plants, mainly solanaceae. [PubChem] Indication: For the treatment of poisoning by susceptible organophosphorous nerve agents having cholinesterase activity as well as organophosphorous or carbamate insecticides. Atropine, a naturally occurring belladonna alkaloid, is a racemic mixture of equal parts of d- and l-hyoscyamine, whose activity is due almost entirely to the levo isomer of the drug. Atropine is commonly classified as...
- Avapena
- Avirox - Pharmacological action Acyclovir Pharma is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against...
- Azarek
- Azathioprine - SPL UNCLASSIFIED SECTION PRODUCT INFORMATION Rx only WARNING - MALIGNANCY Chronic immunosuppression with IMURAN, a purine antimetabolite increases risk of malignancy in humans. Reports of malignancy include post-transplant lymphoma and hepatosplenic T-cell lymphoma (HSTCL) in patients with inflammatory bowel disease....
- Azithromycin - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- Azithromycin Sandoz Eco - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- Azithromycine
- Azithromycine Monodose
- Azitrohexal
- Azitromicina - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- Azitromycine - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- Azubronchin
- Azubronchin Akut
- Azucimet
- Azudoxat
- Azudoxat Comp.
- Azudoxat-T - Pharmacological action Doxycycline is an semisynthetic tetracycline group's antibiotic of broad-spectrum. This medication has bacteriostatic action due to suppression of protein synthesis of pathogens. It active against aerobic gram-positive bacteria: Staphylococcus spp. (including strains producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae), Bacillus anthracis, Listeria monocytogenes; anaerobic bacteria: Clostridium spp. Doxycycline is also active against...
- Azufibrat
- Azufibrat Retard
- Azuglucon
- Azumetop
- Azumetop HCT
- Azupamil
- Azupentat
- Azuperamid
- Azuranit
- Azutranquil
- Azutrimazol - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Azyth - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- BECeco
- BECeco Easyhaler
- Baclofen - Pharmacological action Baclofen is a centrally acting muscle relaxant; GABA B -receptor agonist. It depresses mono-and polysynaptic reflexes presumably by reducing the release of excitatory amino acids (glutamate and aspartate) from the terminals which occurs as a result of stimulation of presynaptic GABA-receptors. This medication does not affect the transmission of impulses in the nerve-muscle synapses; reduces skeletal muscle tone; has a moderate analgesic effect. Pharmacokinetics ...
- Bacteric - This medication is used to prevent minor skin infections caused by small cuts, scrapes, or burns. Bacitracin works by stopping the growth of certain bacteria. It belongs to a class of drugs known as antibiotics. This antibiotic only prevents bacterial infections . It will not work for virus or fungus infections. Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness. Do not use this product over large areas of the body. Do not use it for serious skin...
- Bacteric F
- Bactoreduct
- Banadoz
- Baneocin
- Baxima
- Beclo
- Beclobreathe
- Beclometason
- Bedranol
- Belladenal
- Belladenal-S
- Bellergal - This medication is used to relieve symptoms related to nervousness and tension. This includes unpleasant menopausal signs (such as hot flashes or flushes, sweats, restlessness, trouble sleeping), heart / blood vessel disorders (such as fast/pounding heartbeat), stomach /intestinal disorders (such as spasms), and throbbing headaches that occur often. Ergotamine and belladonna work by blocking certain chemicals (e.g., acetylcholine) in the nervous system to help relieve these...
- Benazepril - Benazepril information Benazepril is a drug belonging to the class of ACE (Angiotensin Converting Enzyme) inhibitors. It is used to lower blood pressure. Benazepril indications Benazepril is primarily prescribed for patients suffering from high blood pressure or hypertension. Benazepril may also be used for other purposes aside from treating high blood pressure. Benazepril warnings Benazepril should not be taken when you are pregnant especially on the 2nd and third trimester of...
- Benazepril; Hydrochlorothiazide - This medication is a combination of two drugs, an ACE inhibitor ( benazepril ) and a "water pill"/diuretic ( hydrochlorothiazide ). It is used to treat high blood pressure ( hypertension ). Benazepril works by relaxing blood vessels, causing them to widen. The hydrochlorothiazide diuretic increases the amount of urine you make, therefore decreasing excess water and salt in your body. Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. OTHER USES: ...
- Bendroflumethiazide - A thiazide diuretic with actions and uses similar to those of hydrochlorothiazide. It has been used in the treatment of familial hyperkalemia, hypertension, edema, and urinary tract disorders. (From Martindale, The Extra Pharmacopoeia, 30th ed, p810) Indication: For the treatment of high blood pressure and management of edema related to heart failure. Bendroflumethiazide, a thiazide diuretic, removes excess water from the body by increasing how often you urinate (pass water) and also widens the...
- Benzet
- Benzetacil Combinado
- Betahistine - Betahistine is an antivertigo drug first used for treating vertigo assosicated with MГ©niГЁre’s disease. It is also commonly used for patients with balance disorders. Indication: For the reduction of episodes of vertigo association with MГ©niГЁre's disease. Betahistine primarily acts as a histamine H1-agonist with 0.07 times the activity of histamine. Stimulating the H1-receptors in the inner ear causes a vasodilatory effect and increased permeability in the blood vessels which...
- Betaject
- Betamethason - Betamethasone information Betamethasone is in a class of drugs called steroids. The medicine reduces swelling and decreases the body's immune response. It is used to treat endocrine (hormonal) disorders when the body does not produce enough of its own steroids. It is also used to treat many immune and allergic disorders, such as arthritis, lupus, psoriasis, asthma, ulcerative colitis, and Crohn's disease. Betamethasone warnings If there is a serious bacterial, viral, or fungal...
- Betamethasone CR
- Bethanechol - Bethanechol is a synthetic ester structurally and pharmacologically related to acetylcholine. A slowly hydrolyzed muscarinic agonist with no nicotinic effects, bethanechol is generally used to increase smooth muscle tone, as in the GI tract following abdominal surgery or in urinary retention in the absence of obstruction. It may cause hypotension, cardiac rate changes, and bronchial spasms. [PubChem] Indication: For the treatment of acute postoperative and postpartum nonobstructive (functional)...
- Bexacal
- Bexalcor
- Bexalcor SR
- Bezafibrate - Antilipemic agent that lowers cholesterol and triglycerides. It decreases low density lipoproteins and increases high density lipoproteins. [PubChem] Indication: For the treatment of primary hyperlipidaemia types IIa, IIb, III, IV and V (Fredrickson classification) corresponding to groups I, II and III of the European Atherosclerosis Society guidelines - when diet alone or improvements in lifestyle such as increased exercise or weight reduction do not lead to an adequate response. Also for the...
- Bibloc
- Bicadex - Bicalutamide information Bicalutamide prevents the actions of androgens or male hormones in the body. It is an anti-androgen. Bicalutamide indications This medication is primarily used in the treatment of cancer in the prostate. It may also be used for purposes other than those indicated here. Bicalutamide warnings This drug may not be advisable if you have liver disease or any other serious illness. You may not be able to take this drug, may need dosage adjustments, or may need...
- Bicalutamid - Bicalutamide information Bicalutamide prevents the actions of androgens or male hormones in the body. It is an anti-androgen. Bicalutamide indications This medication is primarily used in the treatment of cancer in the prostate. It may also be used for purposes other than those indicated here. Bicalutamide warnings This drug may not be advisable if you have liver disease or any other serious illness. You may not be able to take this drug, may need dosage adjustments, or may need...
- Bicalutamide - Bicalutamide information Bicalutamide prevents the actions of androgens or male hormones in the body. It is an anti-androgen. Bicalutamide indications This medication is primarily used in the treatment of cancer in the prostate. It may also be used for purposes other than those indicated here. Bicalutamide warnings This drug may not be advisable if you have liver disease or any other serious illness. You may not be able to take this drug, may need dosage adjustments, or may need...
- Bilol
- Bilol Comp
- Bimatoprost - RECENT MAJOR CHANGES Warnings and Precautions, Intraocular Inflammation ( 5.3 ) 09/2014 1 INDICATIONS AND USAGE Bimatoprost ophthalmic solution, 0.03% is a prostaglandin analog indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension. ( 1 ) SPL UNCLASSIFIED...
- Bimoxan
- Binoclar
- Binocrit
- Binozyt - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- Biocef - This medication is used to treat a wide variety of bacterial infections . This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria. This medication will not work for viral infections (such as common cold , flu ). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness. OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by...
- Bioclavid
- Bioclavid Forte
- Biodroxil
- Bonceur
- Boncordin
- Brachont
- Breatheze - Pharmacological action Albuterol Pharmaceuticals is a beta adrenoagonists with a predominant effect on beta2-adrenergic receptors (localized, particularly in the bronchi, myometrium, blood vessels). This medication prevents and reduces or eliminates bronchospasm, reduces the resistance in the airways, increases the vital capacity. It prevents the release of histamine, slow reacting substance from mast cells and factors chemotaxis of neutrophils. Compared with other drugs of this group has...
- Brenax
- Bresben
- Bresben Mite
- Bretylium - Bretylium blocks the release of noradrenaline from the peripheral sympathetic nervous system, and is used in emergency medicine, cardiology, and other specialties for the acute management of ventricular tachycardia and ventricular fibrillation. The primary mode of action for bretylium is thought to be inhibition of voltage-gated K(+) channels. Recent evidence has shown that bretylium may also inhibit the Na,K-ATPase by binding to the extracellular K-site. Indication: For use in the prophylaxis...
- Brimonidine - Brimonidine is a drug used to treat glaucoma. It acts via decreasing aqueous humor synthesis. [Wikipedia] Indication: For the lowering of intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Brimonidine significantly lowers intraocular pressure with minimal effects on cardiovascular and pulmonary parameters. It lowers intraocular pressure by reducing aqueous humor production and increasing uveoscleral outflow.
- Brimonidine; Timolol - This combination medication is used to treat high pressure inside the eye due to glaucoma (open-angle type) or other eye diseases (e.g., ocular hypertension ). Lowering high pressure inside the eye helps to prevent blindness. This product contains brimonidine and timolol . These medications are used together when 1 drug is not controlling the pressure inside the eye. Brimonidine works by allowing better fluid drainage from within the eye and also by decreasing the amount of fluid...
- Bromam
- Bromaze
- Bromazepam - One of the benzodiazepines that is used in the treatment of anxiety disorders. [PubChem] It is a Schedule IV drug in the U.S. and Canada and under the Convention on Psychotropic Substances. Indication: For the short-term treatment of insomnia, short-term treatment of anxiety or panic attacks, if a benzodiazepine is required, and the alleviation of the symptoms of alcohol- and opiate-withdrawal. Bromazepam is a lipophilic, long-acting benzodiazepine and with sedative, hypnotic, anxiolytic and...
- Bromergon
- Bromocriptine - Bromocriptine mesylate is a semisynthetic ergot alkaloid derivative with potent dopaminergic activity. It is indicated for the management of signs and symptoms of Parkinsonian Syndrome. Bromocriptine also inhibits prolactin secretion and may be used to treat dysfunctions associated with hyperprolactinemia. It also causes sustained suppression of somatotropin (growth hormone) secretion in some patients with acromegaly. Bromocriptine has been associated with pulmonary fibrosis. Indication: For...
- Bromocriptine-BC
- Brompheniramine - Histamine H1 antagonist used in treatment of allergies, rhinitis, and urticaria. [PubChem] Indication: For the treatment of the symptoms of the common cold and allergic rhinitis, such as runny nose, itchy eyes, watery eyes, and sneezing. Brompheniramine is an antihistaminergic medication of the propylamine class. It is a first-generation antihistamine. In allergic reactions an allergen interacts with and cross-links surface IgE antibodies on mast cells and basophils. Once the mast...
- Bronchophen
- Brozam
- Budesonid
- Budesonide - 1 INDICATIONS AND USAGE ENTOCORT EC is a glucocorticosteroid indicated for: • Treamtment of mild to moderate active Crohn’s disease involving the ileum and/or the ascending colon. (1.1) • Maintenance of clinical remission of mild to moderate Crohn’s disease involving the ileum and/or the ascending...
- Budesonide Easyhaler
- Bufexan
- Bumetanide - SPL UNCLASSIFIED SECTION Rx Only WARNING Bumetanide is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required, and dose and dosage...
- Bupropion - A unicyclic, aminoketone antidepressant. The mechanism of its therapeutic actions is not well understood, but it does appear to block dopamine uptake. The hydrochloride is available as an aid to smoking cessation treatment. [PubChem] Indication: For the treatment of depression and as aid to smoking cessation. Bupropion, an antidepressant of the aminoketone class and a non-nicotine aid to smoking cessation, is chemically unrelated to tricyclic, tetracyclic, selective serotonin re-uptake...
- Bupropion ER
- Bupropion SR - Bupropion belongs to the family of medications known as antidepressants . It is used to treat depression . It works by affecting the balance of chemicals that occur naturally in the brain. For the treatment of depression, the full effects of the medication may not be seen until after several weeks of treatment. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used...
- Buspirone - An anxiolytic agent and a serotonin receptor agonist belonging to the azaspirodecanedione class of compounds. Its structure is unrelated to those of the benzodiazepines, but it has an efficacy comparable to diazepam. [PubChem] Indication: For the management of anxiety disorders or the short-term relief of the symptoms of anxiety, and also as an augmention of SSRI-treatment against depression. Buspirone is used in the treatment of generalized anxiety where it has advantages over other...
- Butabarbital - Butabarbital (trade name Butisol) is a prescription barbiturate sleep aid. Butabarbital has a particularly fast onset of effects and short duration of action compared to other barbiturates, which makes it useful for certain applications such as treating severe insomnia and relieving anxiety before surgical procedures; however it is also relatively dangerous particularly when combined with alcohol, and so is now rarely used, although it is still prescribed in some Eastern European and South...
- Butal Compound
- Butazolidina
- CEC
- CEC Forte
- Ca-C 1000
- Cafergot-PB Suppositories
- Cafergot-PB Tablets
- Cafergot-PP
- Calcium C
- Calcium D Sandoz
- Calcium D3 Sandoz
- Calcium Injections
- Calcium Sandoz
- Calcium Sandoz + D
- Calcium Sandoz + Vit C
- Calcium Sandoz + Vitamin C
- Calcium Sandoz + Vitamina C
- Calcium Sandoz + Vitamine C
- Calcium Sandoz C
- Calcium Sandoz D Osteo
- Calcium Sandoz D Osteo Intens
- Calcium Sandoz D3
- Calcium Sandoz D3 Citro
- Calcium Sandoz D3 F
- Calcium Sandoz D3 F Aprikose
- Calcium Sandoz D3 F Instant
- Calcium Sandoz D3 F Orange
- Calcium Sandoz D3 FF
- Calcium Sandoz D3 FF Instant
- Calcium Sandoz D3 Forte
- Calcium Sandoz D3 Forte Orange
- Calcium Sandoz F
- Calcium Sandoz F Citron
- Calcium Sandoz F Nature
- Calcium Sandoz FF
- Calcium Sandoz FF Citron
- Calcium Sandoz FF Nature
- Calcium Sandoz Formel +
- Calcium Sandoz Forte
- Calcium Sandoz Forte D
- Calcium Sandoz Fortisimo
- Calcium Sandoz Fortissimum
- Calcium Sandoz Sun
- Calcium Sandoz Sun and Day
- Calcium Sandoz Woman
- Calcium Syrup
- Calcium Vitamine D3
- Calcium Vitamine D3 GNR
- Calcos Vitamine D3
- Calsan
- Captohexal
- Captohexal Cor
- Captol
- Captopril - SPL UNCLASSIFIED SECTION CAPTOPRIL TABLETS, USP Rev. 03/16 Rx Only WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue captopril tablets as soon as possible. • Drugs...
- Captopril HCT
- Captopril Hctz
- Captopril; Hydrochlorothiazide - This medication is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications, captopril and hydrochlorothiazide . Captopril belongs to a class of drugs known as ACE inhibitors . It works by relaxing blood vessels so blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic). This drug increases the amount of urine you make, causing your body to...
- Captoretic
- Captosol
- Captosol Comp.
- Carbamazepine - WARNINGS SERIOUS DERMATOLOGIC REACTIONS AND HLA-B * 1502 ALLELE SERIOUS AND SOMETIMES FATAL DERMATOLOGIC REACTIONS, INCLUDING TOXIC EPIDERMAL NECROLYSIS (TEN) AND STEVENS-JOHNSON SYNDROME (SJS), HAVE BEEN REPORTED DURING TREATMENT WITH CARBAMAZEPINE. THESE REACTIONS ARE ESTIMATED TO OCCUR IN 1 TO 6 PER 10,000 NEW USERS IN COUNTRIES WITH MAINLY CAUCASIAN POPULATIONS, BUT THE RISK IN SOME ASIAN COUNTRIES IS ESTIMATED TO BE ABOUT 10 TIMES...
- Carbamazepine LP
- Carbamazepine Retard
- Carbamazepine-BC
- Carbasalaatcalcium Cardio
- Carbidopa; Levodopa
- Carbidopa; Levodopa CR
- Carbloxal - Carvedilol information Carvedilol is a blood pressure medication and belongs to the class of drugs known as beta-blockers. These beta-blockers affect the circulatory system, which includes the human heart, arteries and veins. Carvedilol indications This medication is used primarily in treating hypertension or high blood pressure. Carvedilol warnings Taking Carvedilol may not be advisable if you have any of the following conditions: asthma heart problems such as low blood pressure...
- Carbo-Dome
- Carbodome
- Carboplatin - SPL UNCLASSIFIED SECTION Rx Only WARNING Carboplatin injection should be administered under the supervision of a qualified physician experienced in the use of cancer chemotherapeutic agents. Appropriate management of therapy and complications is possible only when adequate treatment facilities are readily available. ...
- Carboplatine
- Cardispare
- Cardogrel
- Carisoprodol - Warnings and Precautions, Sedation ( 5.1 ) 10/2009 Warnings and Precautions, Drug Dependence, Withdrawal, and Abuse ( 5.2 ) 10/2009 1 INDICATIONS AND USAGE Carisoprodol Tablets are indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. Carisoprodol Tablets should only be used for short periods (up to...
- Carisoprodol; Aspirin - This product is used short-term to treat muscle pain and discomfort. It is usually used along with rest, physical therapy, and other treatments. Carisoprodol helps to relax the muscles. Aspirin helps to decrease pain and swelling.
- Carisoprodol; Aspirin; Codeine
- Carpaz
- Carsol CR
- Carvedilol - Carvedilol information Carvedilol is a blood pressure medication and belongs to the class of drugs known as beta-blockers. These beta-blockers affect the circulatory system, which includes the human heart, arteries and veins. Carvedilol indications This medication is used primarily in treating hypertension or high blood pressure. Carvedilol warnings Taking Carvedilol may not be advisable if you have any of the following conditions: asthma heart problems such as low blood pressure...
- Carvetone - Carvedilol information Carvedilol is a blood pressure medication and belongs to the class of drugs known as beta-blockers. These beta-blockers affect the circulatory system, which includes the human heart, arteries and veins. Carvedilol indications This medication is used primarily in treating hypertension or high blood pressure. Carvedilol warnings Taking Carvedilol may not be advisable if you have any of the following conditions: asthma heart problems such as low blood pressure...
- Cedilanid Injections
- Cefabiot
- Cefaclor - SPL UNCLASSIFIED SECTION CEFACLOR CAPSULES, USP Rev. 09/15 Rx Only To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefaclor and other antibacterial drugs, cefaclor should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Cefadroxil - SPL UNCLASSIFIED SECTION CEFADROXIL CAPSULES, USP Rev. 01/16 Rx Only To reduce the development of drug resistant bacteria and maintain the effectiveness of cefadroxil capsule and other antibacterial drugs, cefadroxil capsule should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. ...
- Cefalexin-BC
- Cefallone
- Cefazolin - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of Cefazolin for Injection and other antibacterial drugs, Cefazolin for Injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Cefazolin for Injection, USP is a semi-synthetic cephalosporin for parenteral...
- Cefazolin-BC
- Cefdinir - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefdinir and other antibacterial drugs, cefdinir should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Cefdinir capsules contain the active ingredient cefdinir, an extended-spectrum, semisynthetic cephalosporin,...
- Cefepime - 1 INDICATIONS AND USAGE Cefepime for Injection is a cephalosporin antibacterial indicated for the treatment of the following infections caused by susceptible strains of the designated microorganisms: • Pneumonia. ( 1.1 ) • Empiric therapy for febrile neutropenic patients. ( 1.2 ) ...
- Cefotaxime-BC
- Cefpodoxim - This medication is used to treat a wide variety of bacterial infections . This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (e.g., common cold , flu ). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness.
- Cefpodoxime - Cefpodoxime is an oral third generation cephalosporin antibiotic. It is active against most Gram positive and Gram negative bacteria. It is commonly used to treat acute otitis media, pharyngitis, and sinusitis. Cefpodoxime proxetil is a prodrug which is absorbed and de-esterified by the intestinal mucosa to Cefpodoxime. Indication: For the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms. Cefpodoxime is an oral third...
- Cefpodoxime Enfants et Nourrissons
- Cefprozil - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefprozil and other antibacterial drugs, cefprozil should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Cefprozil is a semi-synthetic broad-spectrum cephalosporin antibiotic. Cefprozil is a...
- Ceftazidim
- Ceftazidime - SPL UNCLASSIFIED SECTION TAZICEF ® brand of ceftazidime for injection, USP PRESCRIBING INFORMATION ...
- Ceftriaxon
- Ceftriaxone - SPL UNCLASSIFIED SECTION Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ceftriaxone for Injection, USP and other antibacterial drugs, Ceftriaxone for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Ceftriaxone-BC
- Cefurim Eco
- Cefuroxim
- Cefuroxime - PHARMACY BULK PACKAGE NOT FOR DIRECT INFUSION Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Cefuroxime for Injection, USP and other antibacterial drugs, Cefuroxime for Injection, USP should be used only to treat or...
- Cefuroximnatrium
- Cerebroforte
- Cerebroforte Liquidum
- Cereen - Haloperidol information This medication is used to control tics and vocal utterances that are part of Tourette's syndrome. Haloperidol is used for treating psychotic disorders and for tics and vocal utterances of Tourette's syndrome. Haloperidol warnings Haloperidol causes sedation, and sedation may be greater if haloperidol is taken with alcohol and other drugs than can cause sedation such as the benzodiazepine class of anti-anxiety drugs (e.g., Valium, Ativan, Klonopin, Xanax), the...
- Cerexin
- Cet Eco
- Cetallerg
- Cethexal
- Cetirizin
- Cetirizina
- Cetirizine - Active ingredient (in each 5 mL teaspoonful) Cetirizine HCl 5 mg Purpose Antihistamine Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes ...
- Cetirizine Conseil
- Cetirizine; Pseudoephedrine - This medication is used to relieve allergy symptoms such as watery eyes , runny/stuffy nose, itching eyes/nose, and sneezing. It contains 2 medications: cetirizine and pseudoephedrine . Cetirizine is an antihistamine and works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction . Pseudoephedrine is a decongestant and works by narrowing the blood vessels in the nose to decrease swelling and congestion. This medication is not...
- Cetrixal
- Cetyrol
- Chloordiazepoxide
- Chloortalidon
- Chlordiazepoxide - An anxiolytic benzodiazepine derivative with anticonvulsant, sedative, and amnesic properties. It has also been used in the symptomatic treatment of alcohol withdrawal. [PubChem] Indication: For the management of anxiety disorders or for the short-term relief of symptoms of anxiety, withdrawal symptoms of acute alcoholism, and preoperative apprehension and anxiety. Chlordiazepoxide has antianxiety, sedative, appetite-stimulating and weak analgesic actions. The drug seems to block EEG arousal...
- Chlorpheniramine - A histamine H1 antagonist used in allergic reactions, hay fever, rhinitis, urticaria, and asthma. It has also been used in veterinary applications. One of the most widely used of the classical antihistaminics, it generally causes less drowsiness and sedation than promethazine. [PubChem] Indication: For the treatment of rhinitis, urticaria, allergy, common cold, asthma and hay fever. In allergic reactions an allergen interacts with and cross-links surface IgE antibodies on mast cells and...
- Chlorpromazine - The prototypical phenothiazine antipsychotic drug. Like the other drugs in this class, chlorpromazine’s antipsychotic actions are thought to be due to long-term adaptation by the brain to blocking dopamine receptors. Chlorpromazine has several other actions and therapeutic uses, including as an antiemetic and in the treatment of intractable hiccup. [PubChem] Indication: For the treatment of schizophrenia, control nausea and vomiting, For relief of restlessness and apprehension before...
- Chlorpropamide - DESCRIPTION Chlorpropamide is an oral blood-glucose-lowering drug of the sulfonylurea class. Chlorpropamide, USP is a white, crystalline powder, that has a slight odor. It is practically insoluble in water, but is soluble in alcohol. Chemically, it is 4-chloro- N -[(propyl-amino)carbonyl] benzene sulfonamide which may be represented by the following structure: Chlorpropamide is supplied as compressed...
- Chlorthalidone - Chlorthalidone is an oral antihypertensive/diuretic. It is a monosulfamyl diuretic that differs chemically from thiazide diuretics in that a double-ring system is incorporated in its structure. It is 2-chloro-5(1-hydroxy-3-oxo-1- isoindolinyl) benzenesulfonamide with the following structural formula: Molecular Formula: C 14 H 11 ClN 2 O 4 S Molecular Weight: 338.76 Chlorthalidone, USP is...
- Chlorzoxazone - SPL UNCLASSIFIED SECTION For Painful Musculoskeletal Conditions DESCRIPTION Each caplet (capsule shaped tablet) contains: Chlorzoxazone 5-chlorobenzoxazolinone ...
- Cholestyramine - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Prevalite ® (cholestyramine for oral suspension, USP) powder, the chloride salt of a basic anion exchange resin, a cholesterol-lowering agent, is intended for oral administration. Cholestyramine resin is quite hydrophilic, but insoluble in water. The cholestyramine resin in Prevalite ® (cholestyramine...
- Cholestyramine LT
- Cholestyramine Light - Cholestyramine is used along with a proper diet to lower cholesterol in the blood . Lowering cholesterol helps decrease the risk for strokes and heart attacks . In addition to a proper diet (such as a low-cholesterol/low-fat diet), other lifestyle changes that may help this medication work better include exercising , losing weight if overweight , and stopping smoking . Consult your doctor for more details. Cholestyramine may also be used to treat itching in people with too...
- Chromosol Ophta
- Ciclohexal
- Ciclopirox - illustration 6.6 mL carton week 48 Week 12 Structure DESCRIPTION Ciclopirox Topical Solution, 8%, (Nail Lacquer) contains a synthetic antifungal agent, ciclopirox. It is intended for topical use on fingernails and toenails and immediately adjacent skin. Each gram of Ciclopirox Topical Solution, 8%, (Nail Lacquer), contains 80 mg...
- Ciclosol
- Ciclox - Pharmacological action Clonazepam is an antiepileptic drugs from the group of benzodiazepine derivatives. This medication has a pronounced anticonvulsant and central muscle relaxant, anxiolytic, sedative and hypnotic effects. Clonazepam strengthens the inhibitory effect of GABA on the transmission of nerve impulses. Anxiolytic effects of this drug is due to the influence on the amygdaloid complex of the limbic system and appears in reducing the emotional stress, reduce anxiety, fear,...
- Cidron
- Cilostazol - WARNING: CONTRAINDICATED IN HEART FAILURE PATIENTS Cilostazol is contraindicated in patients with heart failure of any severity. Cilostazol and several of its metabolites are inhibitors of phosphodiesterase III. Several drugs with this pharmacologic effect have caused decreased survival compared to placebo in patients with class III-IV heart failure. ...
- Cimetidine - DESCRIPTION Cimetidine is a histamine H 2 -receptor antagonist. Chemically it is N” -cyano- N -methyl- N’ -[2-[[(5-methyl-1 H -imidazol-4-yl)methyl]thio]-ethyl], guanidine. The molecular formula for cimetidine is C 10 H 16 N 6 S; and the molecular weight is 252.35. The structural formula for cimetidine is: Cimetidine contains an imidazole ring, and is chemically related to histamine. Cimetidine has...
- Cinnarizine - Pharmacological action Cinnarizine is a calcium channel blocker class IV with a predominant effect on the brain vessels, a derivative of piperazine. This medication improves cerebral, coronary and peripheral circulation. Cinnarizine violates the entrance of calcium ions into vascular smooth muscle cells. This drug lowers the tone of arteriolar smooth muscle, decreases the vasoconstrictor response to biogenic substances (epinephrine, norepinephrine, bradykinin). Cinnarizine reduces the...
- Cip Eco
- Cipro-Hexal
- Ciprofloxacin - Chemical Structure WARNING Fluoroquinolones, including Ciprofloxacin Tablets, are associated with an increased risk of tendinitis and tendon rupture in all ages. This risk is further increased in older patients usually over 60 years of age, in patients taking corticosteroid drugs, and in patients with kidney, heart or lung transplants (See WARNINGS ). ...
- Ciprofloxacin Extended Release
- Ciprofloxacin Sandoz Eco - Pharmacological action Ciprofloxacin is a broad-spectrum antimicrobial drug of fluoroquinolone group with bactericidal action. Inhibits DNA gyrase and inhibits the synthesis of bacterial DNA. Highly active against most gram-negative bacteria: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae. Ciprofloxacin is active against Staphylococcus spp. (including strains producing and not producing...
- Ciprofloxacine
- Ciprofloxacino
- Ciprohexal
- Citadur
- Citalon
- Citalopram - Pharmacological action Citalopram is an antidepressant. The mechanism of action is associated with selective blockade of the inverse of neuronal serotonin in the synapses of neurons of the CNS. Citalopram lacks or has a very weak ability to bind to histamine, m-choline- and adrenoreceptors. Pharmacokinetics After oral administration C max of citalopram in plasma is achieved within 2-4 hours. The oral bioavailability is about 80%. Changes in plasma concentrations of citalopram are...
- Citalopram Ecosol
- Citrate de Betaine Conseil
- Citrocit
- Claforan - Cefotaxime is an antibiotic used to treat a wide variety of bacterial infections . This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria.
- Clamycin
- Clarithromycin - DESCRIPTION Clarithromycin is a semi-synthetic macrolide antibiotic. Chemically, it is 6-0-methylerythromycin. The molecular formula is C 38 H 69 NO 13 , and the molecular weight is 747.96. CLINICAL PHARMACOLOGYPharmacokinetics Clarithromycin is rapidly absorbed from the gastrointestinal tract after oral administration. The absolute bioavailability...
- Clarithromycin ER
- Clarithromycine
- Claritromicina
- Claritromycine
- Clatromicin
- Clavamox
- Clemastine - An ethanolamine-derivative, first generation histamine H1 antagonist used in hay fever, rhinitis, allergic skin conditions, and pruritus. It causes drowsiness. [PubChem] Indication: For the relief of symptoms associated with allergic rhinitis such as sneezing, rhinorrhea, pruritus and acrimation. Also for the management of mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Used as self-medication for temporary relief of symptoms associated with the common cold....
- Clenil
- Cletus
- Clidam
- Climacteron
- Clindahexal
- Clindamycin - ZydaClin™ (clindamycin) Oral Drops liquid For Use in Dogs & Cats Equivalent to 25 mg per mL clindamycin ...
- Clindamycine - Clindamycin belongs to the class of medications called antibiotics . It is used to treat infections caused by certain types of bacteria . It is also used before dental procedures or surgery to prevent infections in people who have heart conditions that put them at greater risk of infection. Clindamycin kills bacteria by interfering with how they function. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well,...
- Clizid
- Clocillin
- Clodian
- Clofibrate - A fibric acid derivative used in the treatment of hyperlipoproteinemia type III and severe hypertriglyceridemia. (From Martindale, The Extra Pharmacopoeia, 30th ed, p986) Indication: For Primary Dysbetalipoproteinemia (Type III hyperlipidemia) that does not respond adequately to diet. This helps control high cholesterol and high triglyceride levels. Clofibrate is an antilipidemic agent similar to gemfibrozil. It acts to lower elevated serum lipids by reducing the very low-density lipoprotein...
- Clomhexal
- Clomihexal
- Clomipramine - Clomipramine, the 3-chloro analog of imipramine, is a dibenzazepine-derivative tricyclic antidepressant (TCA). TCAs are structurally similar to phenothiazines. They contain a tricyclic ring system with an alkyl amine substituent on the central ring. In non-depressed individuals, clomipramine does not affect mood or arousal, but may cause sedation. In depressed individuals, clomipramine exerts a positive effect on mood. TCAs are potent inhibitors of serotonin and norepinephrine reuptake....
- Clonazepam - Pharmacological action Clonazepam is an antiepileptic drugs from the group of benzodiazepine derivatives. This medication has a pronounced anticonvulsant and central muscle relaxant, anxiolytic, sedative and hypnotic effects. Clonazepam strengthens the inhibitory effect of GABA on the transmission of nerve impulses. Anxiolytic effects of this drug is due to the influence on the amygdaloid complex of the limbic system and appears in reducing the emotional stress, reduce anxiety, fear,...
- Clonidine - Clonidine information Clonidine is a medicine that is meant to lower the patient's blood pressure. It achieves its purpose as it decreases the levels in which certain chemicals are found in the patient's blood. In this way, the veins and arteries are allowed to widen, enabling the heart to beat regularly. Clonidine indications Clonidine is normally used in the treatment of hypertension (also known as high blood pressure). But Clonidine can also be used for other purposes that have not...
- Clopidogrel - Clopidogrel, an antiplatelet agent structurally and pharmacologically similar to ticlopidine, is used to reduce atherosclerotic events such as myocardial infarction, stroke, and vascular death in patients who have had a recent stroke, recent MI, or have established peripheral vascular disease. Indication: For the reduction of atherosclerotic events (myocardial infarction, stroke, and vascular death) in patients with atherosclerosis documented by recent stroke, recent myocardial infarction, or...
- Clopin Eco
- Clopisan
- Clorazepate - A water-soluble benzodiazepine derivative effective in the treatment of anxiety. It has also muscle relaxant and anticonvulsant actions. [PubChem] Indication: For the management of anxiety disorders or for the short-term relief of the symptoms of anxiety. Also used as adjunctive therapy in the management of partial seizures and for the symptomatic relief of acute alcohol withdrawal. Clorazepate is a member of the group of drugs called benzodiazepines. Pharmacologically, clorazepate has the...
- Cloreto de Potassio Sandoz
- Clorotir
- Clorpax
- Clotrimazole - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Clotrisol - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Clozapine - • Warnings and Precautions, Falls ( 5.4 ) Hepatotoxicity ( 5.12 ) 02/2017 WARNING: SEVERE NEUTROPENIA; ORTHOSTATIC HYPOTENSION, BRADYCARDIA, AND SYNCOPE; SEIZURE; MYOCARDITIS AND CARDIOMYOPATHY; INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED...
- Co-Amoxicillin
- Co-Amoxiclav
- Co-Amoxyclav
- Co-Atenolol
- Co-Codamol
- Co-Codamol Forte
- Co-Dydramol
- Co-Enalapril - Enalapril belongs to the class of medications called angiotensin converting enzyme (ACE) inhibitors . It is used to treat high blood pressure and congestive heart failure. This medication works by relaxing blood vessels and by making the heart pump more efficiently. The injectable form is used to lower high blood pressure when the oral form cannot be used. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well,...
- Co-Enatyrol
- Co-Epril
- Co-Lisinopril
- Co-Ramipril
- Co-Tenidone
- Co-Trimoxazol
- Cocaine - An alkaloid ester extracted from the leaves of plants including coca. It is a local anesthetic and vasoconstrictor and is clinically used for that purpose, particularly in the eye, ear, nose, and throat. It also has powerful central nervous system effects similar to the amphetamines and is a drug of abuse. Cocaine, like amphetamines, acts by multiple mechanisms on brain catecholaminergic neurons; the mechanism of its reinforcing effects is thought to involve inhibition of dopamine uptake....
- Codeine - Codeine belongs to the class of medications called narcotic analgesics ("analgesic" means "pain reliever"). It is used to relieve mild-to-moderate pain. It works by blocking pain signals that are sent out by the brain to various areas of the body. Codeine is also used to control coughing that is not controlled by non-narcotic cough suppressants. It works by acting on the brain to dull the cough reflex.
An opioid analgesic related to morphine but with less potent analgesic properties...
- Codeine; Pseudoephedrine
- Codipar
- Cognitiv
- CombiPack
- Combithyrex
- Cordan
- Coridil
- Coridil Retard
- Corisol - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Corisol 3 - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Coronovo
- Coroval
- Coroval B
- Corphed - This combination medication is used to temporarily relieve symptoms caused by the common cold , flu , allergies , or other breathing illnesses (such as sinusitis , bronchitis ). Antihistamines help relieve watery eyes , itchy eyes/nose/throat, runny nose, and sneezing. Decongestants help to relieve stuffy nose and ear congestion symptoms. If you are self-treating with this medication, carefully read the package instructions to be sure it is right for you before you start using...
- Cortamed
- Cotet Capsules
- Cotrim - This medication is used to treat a wide variety of bacterial infections . It is also used to treat a certain type of pneumonia (pneumocystis pneumonia) in patients with a weakened immune system. This medication is a combination of 2 antibiotics: sulfamethoxazole and trimethoprim . It works by stopping the growth of bacteria and the pneumocystis fungus.
- Covocort - Pharmacological action Hydrocortisone is a glucocorticosteroid. Hydrocortisone inhibits the function of leukocytes and tissue macrophages. The migration of leukocytes in the area of inflammation. Impair the capacity of macrophages to phagocytosis and the formation of interleukin-1. Contributes to the stabilization of lysosomal membranes, thereby reducing the concentration of proteolytic enzymes in the field of inflammation. Decreases capillary permeability due to histamine release....
- Cralsanic
- Creo-Rectal
- Creo-Rectal Adulte
- Creo-Rectal Enfant
- Creo-Rectal Nourrisson
- Cromosol Ophta
- Cromosol UD
- Curam
- Curosurf
- Cyclobenzaprine - Cyclobenzaprine is a skeletal muscle relaxant and a central nervous system (CNS) depressant. Cyclobenzaprine acts on the locus coeruleus where it results in increased norepinephrine release, potentially through the gamma fibers which innervate and inhibit the alpha motor neurons in the ventral horn of the spinal cord. It is structurally similar to Amitriptyline, differing by only one double bond. Indication: For use as an adjunct to rest and physical therapy for relief of muscle spasm...
- Cyclosporine - WARNING Only physicians experienced in management of systemic immunosuppressive therapy for the indicated disease should prescribe Neoral. At doses used in solid organ transplantation, only physicians experienced in immunosuppressive therapy and management of organ transplant recipients should prescribe Neoral. Patients receiving the drug should be managed in facilities equipped and staffed with...
- Cyprelle 35
- Cyproheptadine - A serotonin antagonist and a histamine H1 blocker used as antipruritic, appetite stimulant, antiallergic, and for the post-gastrectomy dumping syndrome, etc. [PubChem] Indication: For treatment of perennial and seasonal allergic rhinitis, vasomotor rhinitis, allergic conjunctivitis due to inhalant allergens and foods, mild uncomplicated allergic skin manifestations of urticaria and angioedema, amelioration of allergic reactions to blood or plasma, cold urticaria, dermatographism, and as therapy...
- Cyproteronacetaat; Ethinylestradiol
- Cyproteronacetat EE
- Cyproterone - An anti-androgen that, in the form of its acetate (cyproterone acetate), also has progestational properties. It is used in the treatment of hypersexuality in males, as a palliative in prostatic carcinoma, and, in combination with estrogen, for the therapy of severe acne and hirsutism in females. [Pubchem] Indication: For the palliative treatment of patients with advanced prostatic carcinoma. Cyproterone is an antiandrogen. It suppresses the actions of testosterone (and its metabolite...
- Cyproterone; Ethinylestradiol
- Dandrid
- Decafen
- Deflazacort - 1 INDICATIONS AND USAGE EMFLAZA is indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 5 years of age and older. EMFLAZA is a corticosteroid indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients 5 years of age and older ( 1 ) 2 ...
- Degoran
- Dehydrated Alcohol - SPL UNCLASSIFIED SECTION Rx only Dehydrated Alcohol Injection, USP consists of not less than 98% by volume of ethanol (ethyl alcohol). Dehydrated alcohol is hypobaric in relation to the cerebrospinal fluid. It is injected proximate to nerve tissues and into spinal subarachnoid spaces to produce degeneration of nerve function (neurolysis) for control of chronic pain. ...
- Delatar
- Delnil
- Demo Cineol
- Demo Cineol Adulte
- Demo Cineol Bebe
- Demo Cineol Enfants
- Depex
- Depressase
- Dermazin
- Dermazole
- Desernil
- Desipramine - Desipramine hydrochloride is a dibenzazepine-derivative tricyclic antidepressant (TCA). TCAs are structurally similar to phenothiazines. They contain a tricyclic ring system with an alkyl amine substituent on the central ring. In non-depressed individuals, desipramine does not affect mood or arousal, but may cause sedation. In depressed individuals, desipramine exerts a positive effect on mood. TCAs are potent inhibitors of serotonin and norepinephrine reuptake. Secondary amine TCAs, such as...
- Desloratadine - 1 INDICATIONS AND USAGE Desloratadine Tablets are indicated for: Seasonal Allergic Rhinitis: relief of nasal and non-nasal symptoms in patients 12 years of age and older. ( 1.1 ) Perennial Allergic Rhinitis: relief of nasal and non-nasal symptoms in patients 12 years of age and older. ( 1.2 ) ...
- Desmopressin - Desmopressin is a chemical that is similar to Antidiuretic Hormone (ADH) which is found naturally in the body. It increases urine concentration and decreases urine production. Desmopressin is used to prevent and control excessive thirst, urination, and dehydration caused by injury, surgery, and certain medical conditions, allowing you to sleep through the night without awakening to urinate. It is also used to treat specific types of diabetes insipidus and conditions after head injury or...
- Desmopressine-acetaat
- Desorelle
- Dexa-Phlogont L
- Dexamethasone - DESCRIPTION Dexamethasone tablets USP, 1.5mg for oral administration. Inactive ingredients are microcrystalline cellulose NF, anhydrous lactose NF, FD&C Red #40 aluminum lake, croscarmellose sodium NF, and magnesium stearate NF. The molecular weight for dexamethasone is 392.47. It is designated chemically as 9-fluoro-11β,17,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione. The empirical formula is C22H29F05 and the structural formula is: ...
- Dexmedetomidine - SPL UNCLASSIFIED SECTION Each mL of SILEO contains 0.09 mg dexmedetomidine (equivalent to 0.1 mg dexmedetomidine hydrochloride). For oromucosal use in dogs only. Not intended for ingestion. SPL UNCLASSIFIED SECTION CAUTION Federal law (USA) restricts this drug to use by or on the order of a licensed veterinarian ...
- Dextin
- Dextroamphetamine - BOXED WARNING AMPHETAMINES HAVE A HIGH POTENTIAL FOR ABUSE. ADMINISTRATION OF AMPHETAMINES FOR PROLONGED PERIODS OF TIME MAY LEAD TO DRUG DEPENDENCE AND MUST BE AVOIDED. PARTICULAR ATTENTION SHOULD BE PAID TO THE POSSIBILITY OF SUBJECTS OBTAINING AMPHETAMINES FOR NON-THERAPEUTIC USE OR DISTRIBUTION TO OTHERS, AND THE DRUGS SHOULD...
- Dextropropoxyphene; Paracetamol
- Dextropropoxyphene; Paracetamol; Cafeine
- Diabetase
- Diafat
- Diaglim
- Dialar
- Diaquel
- Diazepam - SPL UNCLASSIFIED SECTION Fliptop Vial Rx only CIV WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death...
- Dibiglim
- Dibiglim-P
- Dibimet
- Dibimet Plus
- Dicillin
- Diclac
- Diclac Akut
- Diclac Dispers
- Diclac Dispers Akut
- Diclac ID
- Diclac Lipogel
- Diclac Retard
- Diclo-Basan
- Diclo-Basan Retard
- Diclo-Gel
- Diclo-Phlogont
- Diclofenac - Pharmacological action NSAIDs, a derivative of phenylacetic acid, diclofenac has a pronounced anti-inflammatory, analgesic and mild antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to two mechanisms: peripheral (indirectly, through suppression of prostaglandin...
- Diclofenac CR
- Diclofenac SR - Pharmacological action NSAIDs, a derivative of phenylacetic acid, diclofenac has a pronounced anti-inflammatory, analgesic and mild antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to two mechanisms: peripheral (indirectly, through suppression of prostaglandin...
- Diclofenac XL
- Diclofenac XR
- Diclofenac-BC
- Diclofenacnatrium
- Diclofenacnatrium Retard
- Diclofenaco
- Diclohexal
- Diclon
- Diclon Rapid
- Diclophlogont
- Diclophlogont Retard
- Diclophlogont SL
- Dicloxacillin - One of the penicillins which is resistant to penicillinase. [PubChem] Indication: Used to treat infections caused by penicillinase-producing staphylococci which have demonstrated susceptibility to the drug. Dicloxacillin is a beta-lactamase resistant penicillin similar to oxacillin. Dicloxacillin has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of dicloxacillin results from the inhibition of cell wall synthesis and is...
- Dicyclomine - A muscarinic antagonist used as an antispasmodic and in urinary incontinence. It has little effect on glandular secretion or the cardiovascular system. It does have some local anesthetic properties and is used in gastrointestinal, biliary, and urinary tract spasms. [PubChem] Indication: For the treatment of functional bowel/irritable bowel syndromeincluding Colicky abdominal pain; diverticulitis Dicyclomine is an anticholinergic drug, a medication that reduces the effect of acetylcholine, a...
- Difenac
- Diflunisal - Cardiovascular Thrombotic Events Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use (see WARNINGS and PRECAUTIONS ). Diflunisal...
- Digoxin - SPL UNCLASSIFIED SECTION Revised 12/11 Rx Only DESCRIPTION: Digoxin Tablets, USP are one of the cardiac (or digitalis) glycosides, a closely related group of drugs having in common specific effects on the myocardium. These drugs are found in a number of plants. Digoxin is extracted from the leaves of Digitalis lanata. The term “digitalis” is used to designate the whole group of...
- Digoxin C.S.D.
- Digoxina
- Dihydergot
- Dihydrocodeine
- Dihydroergotamine - A 9,10alpha-dihydro derivative of ergotamine. It is used as a vasoconstrictor, specifically for the therapy of migraine disorders. [PubChem] Indication: For the acute treatment of migraine headaches with or without aura and the acute treatment of cluster headache episodes. Dihydroergotamine is indicated for the acute treatment of migraine headaches with or without aura and the acute treatment of cluster headache episodes. Dihydroergotamine binds with high affinity to 5-HT1Da and 5-HT1Db...
- Diklofenak
- Dilahex
- Dilanid
- Diltiazem - A benzothiazepine derivative with vasodilating action due to its antagonism of the actions of the calcium ion in membrane functions. It is also teratogenic. [PubChem] Indication: For the treatment of Hypertension Diltiazem, a benzothiazepine calcium-channel blocker, is used alone or with an angiotensin-converting enzyme inhibitor, to treat hypertension, chronic stable angina pectoris, and Prinzmetal's variant angina. Diltiazem is a non-dihydropyridine (DHP)member of the calcium channel blocker...
- Diltiazem CR
- Diltiazem LP
- Dilzicardin
- Dimenhydrinate - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Dimenhydrinate, an anti-nauseant/antiemetic, is the 8-chlorotheophylline salt of diphenhydramine. It contains not less than 53% and not more than 55.5% of diphenhydramine, and not less than 44% and not more than 47% of 8-chlorotheophylline, calculated on the dried basis. Chemically, it is 8-chlorotheophylline compound with...
- Dimethyl Sulfoxide - SPL UNCLASSIFIED SECTION PRESCRIBING INFORMATION Rx only DESCRIPTION RIMSO-50 ® (dimethyl sulfoxide) (DMSO) 50% w/w Aqueous Solution for intravesical instillation. Each mL contains 0.54 gm dimethyl sulfoxide STERILE AND NON-PYROGENIC. ...
- Diophenyl-T
- Diopred - Prednisolone acetate belongs to the family of medications called corticosteroids and is used for its ability to reduce inflammation in many parts of the body. When used in an eye drop, this medication is used to treat swelling and itching of the eye.
- Diphenhydramine - Pharmacological action Diphenhydramine Xepa-Soul Pattinson is a blocker of histamine H1-receptors. It has antiallergic activity, has a local anesthetic, antispasmodic and mild ganglion blocking action. When Diphenhydramine Xepa-Soul Pattinson administered orally diphenhydramine has a sedative and hypnotic effects, has a moderate antiemetic effect and has a central holinoliticheskoy activity. When applied externally it has antiallergic effect. Pharmacokinetics Diphenhydramine...
- Diphenoxylate; Atropine - This medication is used to treat diarrhea . It helps to decrease the number and frequency of bowel movements. It works by slowing the movement of the intestines . Diphenoxylate is similar to narcotic pain relievers, but it acts mainly to slow the gut. Atropine belongs to a class of drugs known as anticholinergics, which help to dry up body fluids and also slow gut movement.
- Dipyridamol
- Dipyridamole - DESCRIPTION PERSANTINE® (dipyridamole USP) is a platelet inhibitor chemically described as 2,2',2",2"'-[(4,8- Dipiperidinopyrimido[5,4- d ]pyrimidine-2,6-diyl)dinitrilo]-tetraethanol. It has the following structural formula: Dipyridamole is an odorless yellow crystalline powder, having a bitter taste. It is soluble in dilute acids, methanol and chloroform, and practically insoluble in water. PERSANTINE...
- Dipyrol
- Disobrom - This combination medication is used to temporarily relieve symptoms caused by the common cold , flu , allergies , or other breathing illnesses (such as sinusitis , bronchitis ). Antihistamines help relieve watery eyes , itchy eyes/nose/throat, runny nose, and sneezing. Decongestants help to relieve stuffy nose and ear congestion symptoms. If you are self-treating with this medication, carefully read the package instructions to be sure it is right for you before you start using...
- Disopyramide - A class I anti-arrhythmic agent (one that interferes directly with the depolarization of the cardiac membrane and thus serves as a membrane-stabilizing agent) with a depressant action on the heart similar to that of guanidine. It also possesses some anticholinergic and local anesthetic properties. [PubChem] Indication: For the treatment of documented ventricular arrhythmias, such as sustained ventricular tachycardia, ventricular pre-excitation and cardiac dysrhythmias. It is a Class Ia...
- Diutensat
- Diutensat Comp.
- Divalproex - This medication is used to treat seizure disorders, certain psychiatric conditions (manic phase of bipolar disorder), and to prevent migraine headaches. It works by restoring the balance of certain natural substances (neurotransmitters) in the brain.
- Dobutamine - A beta-2 agonist catecholamine that has cardiac stimulant action without evoking vasoconstriction or tachycardia. It is proposed as a cardiotonic after myocardial infarction or open heart surgery. [PubChem] Indication: For inotropic support in the short- term treatment of patients with cardiac decompensation due to depressed contractility resulting either from organic heart disease or from cardiac surgical procedures Dobutamine is a direct-acting inotropic agent whose primary activity results...
- Dobutrex
- Docetaxel - WARNING:TOXIC DEATHS, HEPATOTOXICITY, NEUTROPENIA, HYPERSENSITIVITY REACTIONS, AND FLUID RETENTION The incidence of treatment-related mortality associated with docetaxel therapy is increased in patients with abnormal liver function, in patients receiving higher doses, and in patients with non-small cell lung carcinoma and a history of prior treatment with platinum-based chemotherapy who receive...
- Doloreduct - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Dolotandax
- Domperidon
- Domperidone - SPL UNCLASSIFIED SECTION CAUTION Federal law (USA) restricts this drug to use by or on the order of a licensed veterinarian. For oral use in horses only. DESCRIPTION Domperidone is D 2 dopamine receptor antagonist. Chemically, domperidone is ...
- Donepezil - Donepezil (Aricept), is a centrally acting reversible acetyl cholinesterase inhibitor. Its main therapeutic use is in the treatment of Alzheimer’s disease where it is used to increase cortical acetylcholine. Donepezil is postulated to exert its therapeutic effect by enhancing cholinergic function. This is accomplished by increasing the concentration of acetylcholine through reversible inhibition of its hydrolysis by acetylcholinesterase. If this proposed mechanism of action is correct,...
- Dorcol DM
- Dorzolamide - Dorzolamide is a carbonic anhydrase (CA) inhibitor. It is used in ophthalmic solutions (Trusopt) to lower intraocular pressure (IOP) in open-angle glaucoma and ocular hypertension. Indication: For the treatment of elevated intraocular pressure in patients with ocular hypertension or open-angle glaucoma. Also used prophylatically for the inhibition of perioperative IOP increase (before neodynium yttrium aluminum garnet laser posterior capsulotomy). Dorzolamide is topical CA inhibitor that is...
- Dorzolamide; Timolol
- Dosulfin Bronquial
- Dosulfin Fuerte
- Dotur - Pharmacological action Doxycycline is an semisynthetic tetracycline group's antibiotic of broad-spectrum. This medication has bacteriostatic action due to suppression of protein synthesis of pathogens. It active against aerobic gram-positive bacteria: Staphylococcus spp. (including strains producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae), Bacillus anthracis, Listeria monocytogenes; anaerobic bacteria: Clostridium spp. Doxycycline is also active against...
- Doxazosin - DESCRIPTION Doxazosin mesylate is a quinazoline compound that is a selective inhibitor of the alpha 1 subtype of alpha adrenergic receptors. The chemical name of doxazosin mesylate is 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(1,4-benzodioxan-2-ylcarbonyl) piperazine methanesulfonate. The molecular formula for doxazosin mesylate is C 23 H 25 N 5 O 5 • CH 4 O 3 S and the molecular weight is 547.6. It has the following structure: ...
- Doxazosine Retard
- Doxepin - Doxepin hydrochloride is a dibenzoxepin-derivative tricyclic antidepressant (TCA). TCAs are structurally similar to phenothiazines. They contain a tricyclic ring system with an alkyl amine substituent on the central ring. In non-depressed individuals, doxepin does not affect mood or arousal, but may cause sedation. In depressed individuals, doxepin exerts a positive effect on mood. TCAs are potent inhibitors of serotonin and norepinephrine reuptake. Tertiary amine TCAs, such as doxepin and...
- Doxercalciferol - DESCRIPTION Doxercalciferol, the active ingredient in Hectorol ® , is a synthetic vitamin D 2 analog that undergoes metabolic activation in vivo to form 1α,25-dihydroxyvitamin D 2 (1α,25-(OH) 2 D 2 ), a naturally occurring, biologically active form of vitamin D 2 . Hectorol ...
- Doxorubicine
- Doxycyclin - Pharmacological action Doxycycline is an semisynthetic tetracycline group's antibiotic of broad-spectrum. This medication has bacteriostatic action due to suppression of protein synthesis of pathogens. It active against aerobic gram-positive bacteria: Staphylococcus spp. (including strains producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae), Bacillus anthracis, Listeria monocytogenes; anaerobic bacteria: Clostridium spp. Doxycycline is also active against...
- Doxycycline - Pharmacological action Doxycycline is an semisynthetic tetracycline group's antibiotic of broad-spectrum. This medication has bacteriostatic action due to suppression of protein synthesis of pathogens. It active against aerobic gram-positive bacteria: Staphylococcus spp. (including strains producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae), Bacillus anthracis, Listeria monocytogenes; anaerobic bacteria: Clostridium spp. Doxycycline is also active against...
- Doxyhexal
- Doxyhexal SF
- Doxylar
- Doxysol
- Droperidol - SPL UNCLASSIFIED SECTION Injection, USP For Intravenous or Intramuscular Use Only Ampul R x only WARNING ...
- Duloxetine - WARNING: SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. Increased risk of suicidal thinking and behavior in children, adolescents, and young adults...
- Durodor Retard
- Duvaxan
- DynaCirc - Isradipine is used with or without other medications to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. Isradipine is called a calcium channel blocker. It works by relaxing blood vessels so blood can flow more easily.
- Ebetaxel
- Ebunex
- Ecapril
- Ecobiosan
- Ecobiosan E
- Ecobiosan E600
- Ecodipi - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Ecodipin - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Ecodipin E - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Ecodipin Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Ecodipine - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Ecodolor
- Ecodolor Retard
- Ecodurex
- Ecofenac
- Ecofenac CR
- Ecofenac Lipogel
- Ecofenac Ret
- Ecofenac Retard
- Ecomep - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Ecomucyl
- Econazole - A broad spectrum antimycotic with some action against Gram positive bacteria. It is used topically in dermatomycoses also orally and parenterally. [PubChem] Indication: For topical application in the treatment of tinea pedis, tinea cruris, and tinea corporis caused by Trichophyton rubrum, Trichophyton mentagrophytes, Trichophyton tonsurans, Microsporum canis, Microsporum audouini, Microsporum gypseum, and Epidermophyton floccosum, in the treatment of cutaneous candidiasis, and in the treatment...
- Econazole LP
- Ecoprofen - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ecovent
- Ecovent Easyhaler
- Edicin
- Efryl Rhume
- Eisen-Sandoz
- Elcoman
- Embolex LM
- Enahexal
- Enalapril - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Enalapril Comp
- Enalapril HCT
- Enalapril Hctz
- Enalapril-BC
- Enalapril; Hydrochlorothiazide - This medication is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains 2 medications, enalapril and hydrochlorothiazide . Enalapril belongs to a class of drugs known as ACE inhibitors . It works by relaxing blood vessels so that blood can flow through the body more easily. Hydrochlorothiazide is a "water pill" (diuretic) and causes your body to get rid of extra salt and...
- Enalaprilmaleaat
- Enalaprilmaleaat HCT
- Endep - This medication is used to treat mental/mood problems such as depression. It may help improve mood and feelings of well-being, relieve anxiety and tension, help you sleep better, and increase your energy level. This medication belongs to a class of medications called tricyclic antidepressants. It works by affecting the balance of certain natural chemicals (neurotransmitters such as serotonin) in the brain . OTHER USES: This section contains uses of this drug that are not listed in the...
- Endoxan
- Enoxaparin preservative free
- Ephedrine - An alpha- and beta-adrenergic agonist that may also enhance release of norepinephrine. It has been used in the treatment of several disorders including asthma, heart failure, rhinitis, and urinary incontinence, and for its central nervous system stimulatory effects in the treatment of narcolepsy and depression. It has become less extensively used with the advent of more selective agonists. [PubChem] Indication: Ephedrine commonly used as a stimulant, appetite suppressant, concentration aid,...
- Epinastine - Epinastine is used for the prevention of itching associated with allergic conjunctivitis. It has a multi-action effect that inhibits the allergic response in 3 ways: 1. stabilizes mast cells by preventing mast cell degranulation to control the allergic response, 2. prevents histamine binding to both the H1- and H2-receptors to stop itching and provide lasting protection, and 3. prevents the release of proinflammatory chemical mediators from the blood vessel to halt progression of the allergic...
- Epirubicine
- Eplerenone - 1 INDICATIONS AND USAGE Eplerenone tablets are an aldosterone antagonist indicated for: • Improving survival of stable patients with LV systolic dysfunction (LVEF less than or equal to 40%) and CHF after an acute myocardial infarction. (1.1) • the treatment of hypertension,...
- Epril - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Epril Mite - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Epril Plus
- Epril Submite - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Errolon - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Errolon A
- Erybesan
- Erythrogenat
- Erythrogenat TS
- Erythromycin - SPL UNCLASSIFIED SECTION Film-coated Tablets Rx only To reduce the development of drug-resistant bacteria and maintain the effectiveness of Erythromycin Tablets and other antibacterial drugs, Erythromycin Tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Erythromycin; Benzoyl Peroxide - This product is used to treat moderate acne . It helps to reduce the number of pimples. This medication is a combination of 2 drugs. Erythromycin works by stopping the growth of acne-causing bacteria. It belongs to a class of drugs known as macrolide antibiotics. Benzoyl peroxide also kills acne-causing bacteria and causes the top layer of skin to dry and peel off so that new skin can form. This product also contains alcohol which helps to dry extra oils from the skin.
- Erytromycine - Pharmacological action Erythromycin is a macrolide antibiotic. Has bacteriostatic action. However at higher doses against susceptible organisms has a bactericidal effect. erythromycin is reversibly bound to the ribosome of bacteria, thereby inhibiting protein synthesis. Erythromycin is active against gram-positive bacteria: Staphylococcus spp. (strains producing and not producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae); gram-negative bacteria: Neisseria...
- Escitalopram - Warnings and Precautions ( 5.2 ) 1/2017 ...
- Estradiol - SPL UNCLASSIFIED SECTION ESTROGENS INCREASE THE RISK OF ENDOMETRIAL CANCER Close clinical surveillance of all women taking estrogens is important. Adequate diagnostic measures, including endometrial sampling when indicated, should be undertaken to rule out malignancy in all cases of undiagnosed persistent or recurring abnormal vaginal bleeding. There is no evidence that...
- Estramon
- Estramon TTS
- Estramon Uno
- Estranor
- Estranor Eco
- Estulic
- Etiasa
- Etidrel
- Etidrel Kit
- Etidronate
- Etisec
- Etodolac - Cardiovascular Thrombotic Events Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use (see WARNINGS and ...
- Euclugon
- Ex-Lax Light
- Excillin
- Exoderil
- Exodril
- Exogran
- Eyelube
- Ezul
- Famotidine - DESCRIPTION The active ingredient in PEPCID* Registered trademark of Merck Sharp and Dohme Corp, a subsidiary of Merck & Co. Inc. and is used under license. (famotidine) is a histamine H 2 ‑receptor antagonist. Famotidine is N -(aminosulfonyl)-3-[[[2-[(diaminomethylene)amino]-4-thiazolyl]methyl]thio]propanimidamide. The empirical formula of famotidine is C 8 H 15 N 7 O 2 S 3 and its molecular weight is 337.43. Its structural...
- Fantamax
- Favistan
- Felodil
- Felodil Retard
- Felodipin - Felodipine is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. Felodipine is known as a calcium channel blocker. By blocking calcium, this medication relaxes and widens blood vessels so blood can flow more easily. OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care...
- Felodipin Eco
- Felodipine - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Felodipine is a calcium antagonist (calcium channel blocker). Felodipine is a dihydropyridine derivative that is chemically described as ± ethyl methyl 4-(2,3-dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate. Its molecular formula is C 18 H 19 Cl 2 NO 4 and its structural formula is: ...
- Felodipine L.P.
- Felodipine Retard
- Felodipino
- Femanest
- Femanor
- Femasekvens
- Femerin
- Feminil
- Feminil Mite
- Fenahex
- Fenicol
- Fenofibrate - 1 INDICATIONS AND USAGE Fenofibrate tablets are a peroxisome proliferator receptor alpha (PPARα) activator indicated as an adjunct to diet: To reduce elevated LDL-C, Total-C, TG and Apo B, and to increase HDL C in adult patients with primary hypercholesterolemia or...
- Fenoldopam - A dopamine D1 receptor agonist that is used as an antihypertensive agent. It lowers blood pressure through arteriolar vasodilation. [PubChem] Indication: For the in-hospital, short-term (up to 48 hours) management of severe hypertension when rapid, but quickly reversible, emergency reduction of blood pressure is clinically indicated, including malignant hypertension with deteriorating end-organ function. Fenoldopam is an agonist at D1-like dopamine receptors, binds to α2-adrenoceptors,...
- Fenoprofen - SPL UNCLASSIFIED SECTION Rx only Cardiovascular Risk Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may increase with duration of use. Patients with...
- Fenprocoumon
- Fensol
- Fentanyl - SPL UNCLASSIFIED SECTION For Topical Application in Dogs Only Opioid Analgesic NOT FOR INJECTION 50 mg/mL (500 mg/10 mL) CAUTION: Federal law restricts this drug to use by or on the order of a licensed...
- Fentanyl Sandoz MAT
- Ferrofumaraat
- Ferrous Sulphate
- Ferrum Sandoz
- Fexofenadine - Fexofenadine hydrochloride (Allegra) is an antihistamine drug used in the treatment of hayfever and similar allergy symptoms. It was developed as a successor of and alternative to terfenadine. Fexofenadine, like other second and third-generation antihistamines, does not readily pass through the blood-brain barrier, and so causes less drowsiness than first-generation histamine-receptor antagonists. Indication: For management of Seasonal allergic rhinitis Fexofenadine is a second-generation, long...
- Fexofenadine; Pseudoephedrin - This medication is used to relieve allergy symptoms such as watery eyes , runny/stuffy nose, itching eyes/nose, and sneezing. It contains 2 medications: fexofenadine and pseudoephedrine . Fexofenadine is an antihistamine and works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction . Pseudoephedrine is a decongestant and works by narrowing the blood vessels in the nose to decrease swelling and congestion. This medication is not...
- Fibrazate
- Finasterid
- Finasteride - 1 INDICATIONS AND USAGE PROSCAR, is a 5α-reductase inhibitor, indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to ( 1.1 ): Improve symptoms Reduce the risk of acute urinary retention Reduce the risk of the need for surgery including transurethral resection of the prostate (TURP)...
- Flecainide - A potent anti-arrhythmia agent, effective in a wide range of ventricular and atrial arrhythmias and tachycardias. Paradoxically, however, in myocardial infarct patients with either symptomatic or asymptomatic arrhythmia, flecainide exacerbates the arrhythmia and is not recommended for use in these patients. [PubChem] Indication: Flecainide is is a class Ic antiarrhythmic agent and as such, it is used for the prevention of paroxysmal supraventricular tachycardias (PSVT), including...
- Flecainide-Acetaat
- Flox-Ex
- Floxbio - Pharmacological action Ciprofloxacin is a broad-spectrum antimicrobial drug of fluoroquinolone group with bactericidal action. Inhibits DNA gyrase and inhibits the synthesis of bacterial DNA. Highly active against most gram-negative bacteria: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae. Ciprofloxacin is active against Staphylococcus spp. (including strains producing and not producing...
- Flucess - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Flucillin
- Flucloxacillin - Antibiotic analog of cloxacillin. [PubChem] Indication: Used to treat bacterial infection by susceptible microorganisms. Flucloxacillin is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms. The name "penicillin" can either refer to several variants of penicillin available, or to the group of antibiotics derived from the penicillins. Flucloxacillin has in vitro activity against gram-positive and gram-negative...
- Flucloxacilline
- Fluco - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fluconazol - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fluconazol Eco - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fluconazole - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fludarabine - Fludarabine (marketed as fludarabine phosphate under the trade name Fludara) is a chemotherapy drug used in the treatment of hematological malignancies. [Wikipedia] Indication: For the treatment of adult patients with B-cell chronic lymphocytic leukemia (CLL) who have not responded to or whose disease has progressed during treatment with at least one standard alkylating-agent containing regimen Fludarabine is a chemotherapy drug used in the treatment of chronic lymphocytic leukemia. It acts at...
- Fluhexal - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Flumazenil - DESCRIPTION Flumazenil injection is a benzodiazepine receptor antagonist. Chemically, flumazenil is ethyl 8-fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a](1,4) benzodiazepine-3-carboxylate. Flumazenil has an imidazobenzodiazepine structure, a calculated molecular weight of 303.3 and the following structural formula: C 15 H 14 FN 3 O 3 ...
- Flumox
- Flunitrazepam - A benzodiazepine with pharmacologic actions similar to those of diazepam that can cause anterograde amnesia. Some reports indicate that it is used as a date rape drug and suggest that it may precipitate violent behavior. The United States Government has banned the importation of this drug. [PubChem] Indication: For short-term treatment of severe insomnias, that are not responsive to other hypnotics. Flunitrazepam is a powerful hypnotic drug that is a benzodiazepine derivative. It has powerful...
- Flunizol - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fluorouracil - Dosage and Administration ( 2 ) 07/2016 1 INDICATIONS AND USAGE Adrucil (fluorouracil injection) is indicated for the treatment of patients with: Adrucil ® (fluorouracil injection) is a nucleoside metabolic inhibitor indicated for the treatment of...
- Fluoxetin
- Fluoxetina
- Fluoxetine - Pharmacological action Fluoxetine is an antidepressant, propylamine derivative. The mechanism of action is associated with selective blockade of the inverse of neuronal serotonin reuptake in the CNS. Fluoxetine is a weak antagonist of choline, adrenergic and histamine receptors. Unlike most antidepressants fluoxetine apparently does not cause reduction of functional activity of postsynaptic beta-adrenergic receptors. This medication improves mood, reduces anxiety and stress, eliminates...
- Fluoxetine-BC
- Fluphenazine - A phenothiazine used in the treatment of psychoses. Its properties and uses are generally similar to those of chlorpromazine. [PubChem] Indication: For management of manifestations of psychotic disorders. Fluphenazine is a trifluoro-methyl phenothiazine derivative intended for the management of schizophrenia and other psychotic disorders. Fluphenazine has not been shown effective in the management of behaviorial complications in patients with mental retardation.
- Flurazepam - A benzodiazepine derivative used mainly as a hypnotic. [PubChem] Indication: For short-term and intermittent use in patients with recurring insomnia and poor sleeping habits Flurazepam, a benzodiazepine derivative, is a hypnotic agent which does not appear to decrease dream time as measured by rapid eye movements (REM). Furthermore, it decreases sleep latency and number of awakenings for a consequent increase in total sleep time.
- Flurbiprofen - Boxed Warning 5/2016 Warnings and Precautions, Cardiovascular Thrombotic Events ( 5.1 ) 5/2016 Warnings and Precautions, Heart Failure and Edema ( 5.5 ) 5/2016 WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS ...
- Flusol
- Flutahexal
- Flutamide - SPL UNCLASSIFIED SECTION Flutamide Capsules, USP Rx only Revised: July 2014 195814-2 Rx only WARNINGS: Hepatic Injury: There have been postmarketing reports of hospitalization...
- Flutepan
- Fluticasone - Fluticasone is used to control and prevent symptoms (such as wheezing and shortness of breath) caused by asthma . It works by reducing swelling (inflammation) of the airways in the lungs to make breathing easier. Controlling symptoms of asthma helps you maintain your normal activities and decreases time lost from work or school. Fluticasone belongs to a class of drugs known as corticosteroids. This medication must be used regularly to be effective. It does not work immediately and should...
- Fluticasonpropionaat
- Fluvastatin - 1 INDICATIONS AND USAGE Therapy with lipid-altering agents should be only one component of multiple risk factor intervention in individuals at significantly increased risk for atherosclerotic vascular disease due to hypercholesterolemia. Drug therapy is indicated as an adjunct to diet when the response to a diet restricted in saturated fat and cholesterol and other non-pharmacologic measures alone has been inadequate. ...
- Fluvastatin Mite
- Fluvastatine
- Fluvoxamina
- Fluvoxamine - Fluvoxamine is an antidepressant which functions pharmacologically as a selective serotonin reuptake inhibitor. Though it is in the same class as other SSRI drugs, it is most often used to treat obsessive-compulsive disorder.Fluvoxamine has been in use in clinical practice since 1983 and has a clinical trial database comprised of approximately 35,000 patients. It was launched in the US in December 1994 and in Japan in June 1999. As of the end of 1995, more than 10 million patients worldwide...
- Fluvoxaminemaleaat
- Fluxes - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Fluzol - Pharmacological action Fluconazole is an antifungal drug from the group of triazole derivatives. Inhibits the synthesis of ergosterol disrupting the permeability of the cell wall. This medication is active against Candida, Microsporum, Cryptococcus neoformans, Trichophyton. Pharmacokinetics Fluconazole is well absorbed after oral administration. Simultaneous ingestion does not affect absorption. The bioavailability is 90%. Fluconazole is widely distributed in tissues and organs of the...
- Folinate de Calcium
- Foliumzuur
- Foltrin - This medication is a multivitamin product used to treat or prevent low blood levels of iron (e.g., for anemia or during pregnancy ). Iron is an important mineral the body needs to produce red blood cells and keep you in good health. Vitamin C improves the absorption of iron from the stomach . Vitamin B12 is important for growth, cell production, and nerve function. Intrinsic factor is identical to a substance that is made naturally in the stomach. It improves the absorption of...
- Fondur
- Foristal
- Foristal Lontabs
- Formax
- Formoterol Easyhaler
- Forpyn
- Fortalidon
- Fosfomycin - An antibiotic produced by Streptomyces fradiae. [PubChem] Indication: For the treatment of uncomplicated urinary tract infections (acute cystitis) in women due to susceptible strains of Escherichia coli and Enterococcus faecalis. Fosfomycin is a broad spectrum antibiotic that concentrates in kidney and bladder and is used to treat uncomplicated urinary tract infections. Fosfomycin also reduces nephrotoxicity and ototoxicity of platinum-containing anti-tumor agents.
- Fosinopril - WARNING: FETAL TOXICITY When pregnancy is detected, discontinue fosinopril sodium tablets as soon as possible. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. See WARNINGS: Fetal Toxicity ...
- Fosinoprilnatrium
- Frisium - Clobazam belongs to the class of medications known as benzodiazepines . It is used to treat certain seizure disorders. It is used as an add-on to other antiseizure medications when extra treatment for control of seizures is needed. Seizures are caused by uncontrolled firing of neurons in the brain (also referred to as increased electrical activity in the brain). This medication works by reducing the rate of firing of these neurons. Your doctor may have suggested this medication for...
- Frusemide-BC - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Fungicil
- Funginix - Terbinafine information Terbinafine is an antifungal drug used as athlete's foot medication. Terbinafine works like an antibiotic to treat fungal infections. Terbinafine indications This medicine is mainly indicated to treat fungal infections of the fingernails and toenails. Terbinafine may also be used for purposes not mentioned here. Terbinafine warnings This drug is classed as a FDA pregnancy category B drug and may cause severe side effects to an unborn baby. Consult with your...
- Fungireduct
- Furo-Basan - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Furosemide - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Furosemide Special - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Fursol - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- GEA
- Gabadoz - Pharmacological action Gabapentin is an antiepileptic drug. Chemical structure is similar to GABA fulfilling the function of the inhibitory neurotransmitter in the CNS. It is believed that the mechanism of action of Gabapentin is different from other anticonvulsants acting through GABA synapses (including valproate, barbiturates, benzodiazepines, inhibitors of GABA-transaminase, inhibitors of GABA capture, GABA agonists and prodrugs of GABA). In in vitro studies showed that Gabapentin is...
- Gabapentin - Pharmacological action Gabapentin is an antiepileptic drug. Chemical structure is similar to GABA fulfilling the function of the inhibitory neurotransmitter in the CNS. It is believed that the mechanism of action of Gabapentin is different from other anticonvulsants acting through GABA synapses (including valproate, barbiturates, benzodiazepines, inhibitors of GABA-transaminase, inhibitors of GABA capture, GABA agonists and prodrugs of GABA). In in vitro studies showed that Gabapentin is...
- Gabapentina - Pharmacological action Gabapentin is an antiepileptic drug. Chemical structure is similar to GABA fulfilling the function of the inhibitory neurotransmitter in the CNS. It is believed that the mechanism of action of Gabapentin is different from other anticonvulsants acting through GABA synapses (including valproate, barbiturates, benzodiazepines, inhibitors of GABA-transaminase, inhibitors of GABA capture, GABA agonists and prodrugs of GABA). In in vitro studies showed that Gabapentin is...
- Gabapentine - Pharmacological action Gabapentin is an antiepileptic drug. Chemical structure is similar to GABA fulfilling the function of the inhibitory neurotransmitter in the CNS. It is believed that the mechanism of action of Gabapentin is different from other anticonvulsants acting through GABA synapses (including valproate, barbiturates, benzodiazepines, inhibitors of GABA-transaminase, inhibitors of GABA capture, GABA agonists and prodrugs of GABA). In in vitro studies showed that Gabapentin is...
- Gabexal - Pharmacological action Gabapentin is an antiepileptic drug. Chemical structure is similar to GABA fulfilling the function of the inhibitory neurotransmitter in the CNS. It is believed that the mechanism of action of Gabapentin is different from other anticonvulsants acting through GABA synapses (including valproate, barbiturates, benzodiazepines, inhibitors of GABA-transaminase, inhibitors of GABA capture, GABA agonists and prodrugs of GABA). In in vitro studies showed that Gabapentin is...
- Galantamine - Galantamine information Galantamine is a popular medicine that is able to effectively reverse or at least delay mental decline in the case of patients who are suffering from Alzheimer's disease. This medicine achieves its goal by boosting the patient's acetylcholine brain levels. Galantamine indications Galantamine is a popular drug that is generally prescribed to patients who are suffering from Alzheimer's disease. However, this product is only a temporary remedy, as it is unable to...
- Gastrotranquil
- Gastrotranquil Retard
- Geavir
- Gemcit - Gemcitabine is used alone or with other treatments/ medications to treat certain types of cancer (including breast , lung , ovarian, pancreatic). It is a chemotherapy drug that works by slowing or stopping the growth of cancer cells. OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it...
- Gemcitabin - Gemcitabine is used alone or with other treatments/ medications to treat certain types of cancer (including breast , lung , ovarian, pancreatic). It is a chemotherapy drug that works by slowing or stopping the growth of cancer cells. OTHER USES: This section contains uses of this drug that are not listed in the approved professional labeling for the drug but that may be prescribed by your health care professional. Use this drug for a condition that is listed in this section only if it...
- Gemcitabine - • Dosage and Administration, Dose Modifications for Non-Hematologic Adverse Reactions ( 2.5 ) 5/2014 • Warnings and Precautions, Capillary Leak Syndrome ( 5.9 )...
- Gemfibrozil - Gemfibrozil information Gemfibrozil is a drug which is usually prescribed along with a diet to people who have very high levels of serum triglycerides (triglycerides are fatty substances from the blood) and who are at a risk of developing pancreatitis (this is the inflammation of the pancreas). This medication may also be used in order to reduce the risk of developing coronary heart disease in people who have not responded to the other therapy options: weight loss, exercises, and diet and...
- Gemfibrozil-BC - Gemfibrozil information Gemfibrozil is a drug which is usually prescribed along with a diet to people who have very high levels of serum triglycerides (triglycerides are fatty substances from the blood) and who are at a risk of developing pancreatitis (this is the inflammation of the pancreas). This medication may also be used in order to reduce the risk of developing coronary heart disease in people who have not responded to the other therapy options: weight loss, exercises, and diet and...
- Gencin
- Gentamicin - Gentamicin Sulfate Solution 100 mg/mL Gentamicin Sterile Multiple Dose Vial For Use in Horses Only For intra-uterine use in horses only. CAUTION : Federal law restricts this drug to use by or on the order of a licensed veterinarian. ...
- Gentamicine
- Gepeprostin - Bicalutamide information Bicalutamide prevents the actions of androgens or male hormones in the body. It is an anti-androgen. Bicalutamide indications This medication is primarily used in the treatment of cancer in the prostate. It may also be used for purposes other than those indicated here. Bicalutamide warnings This drug may not be advisable if you have liver disease or any other serious illness. You may not be able to take this drug, may need dosage adjustments, or may need...
- Gestodene; Ethinylestradiol
- Gestonette
- Gillazym
- Gingium
- Gingium Intens
- Gingium Spezial
- Ginkgo
- Ginkodilat
- Glaucosan
- Gliben
- Glibenclamid
- Glibenclamide
- Gliclazide - Gliclazide is an oral antihyperglycemic agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM). It belongs to the sulfonylurea class of insulin secretagogues, which act by stimulating β cells of the pancreas to release insulin. Sulfonylureas increase both basal insulin secretion and meal-stimulated insulin release. Medications in this class differ in their dose, rate of absorption, duration of action, route of elimination and binding site on their target pancreatic...
- Gliclazide LM
- Glihexal
- Glimepirid - Glimepiride is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes (non- insulin -dependent diabetes ). It may also be used with other diabetes medications . Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart attack or stroke . Glimepiride belongs to the class of drugs known as...
- Glimepiride - 1 INDICATIONS AND USAGE Glimepiride tablets USP are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus [see Clinical Studies (14.1) ]. Glimepiride is a sulfonylurea indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes...
- Glimexal
- Glipizide - SPL UNCLASSIFIED SECTION For Oral Use DESCRIPTION GLUCOTROL (glipizide) is an oral blood-glucose-lowering drug of the sulfonylurea class. The Chemical Abstracts name of glipizide is 1-cyclohexyl-3-[[p-[2-(5-methylpyrazine-carboxamido)ethyl]phenyl]sulfonyl]urea. The molecular formula is C 21 H 27 N 5 O 4 S; the molecular weight is...
- Glipizide; Metformin - This anti-diabetic medication is a combination of 2 drugs ( glipizide and metformin). It is used along with a diet and exercise program to control high blood sugar in patients with type 2 diabetes (non- insulin -dependent diabetes ). Glipizide is a sulfonylurea and works by stimulating the release of your body's natural insulin and by decreasing the amount of sugar that your liver makes. Metformin is a biguanide and works by decreasing the amount of sugar that your liver makes and that...
- Glutethimide - A hypnotic and sedative. Its use has been largely superseded by other drugs. [PubChem] Indication: For the treatment of insomnia. Glutethimide is a hypnotic sedative that was introduced in 1954 as a safe alternative to barbiturates to treat insomnia. Before long, however, it had become clear that glutethimide was just as likely to cause addiction and caused similarly severe withdrawal symptoms.
- Glyben
- Glyburide - DESCRIPTION Glyburide tablets USP contain glyburide, which is an oral blood-glucose-lowering drug of the sulfonylurea class. Glyburide is a white, crystalline compound. The chemical name for glyburide is 1-[[p-[2-(5-chloro-o-anisamido)ethyl]phenyl]-sulfonyl]-3-cyclohexylurea and the molecular weight is 493.99. It has the following structural formula: Molecular formula: C 23 H 28 ClN 3 O 5 S Each tablet,...
- Glyburide; Metformin - This combination medication is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes (non- insulin -dependent diabetes ). It may also be used with other diabetes medications. This product contains 2 medications. Glyburide belongs to the class of drugs known as sulfonylureas. It lowers blood sugar by causing the release of your body's natural insulin and by decreasing the amount of sugar that your liver makes. Metformin works by...
- Glycopyrrolate - Glycopyrrolate tablets contain the synthetic anticholinergic glycopyrrolate. Glycopyrrolate is a quaternary ammonium compound with the following chemical name: 3-[(cyclopentylhydroxyphenylacetyl)oxy]-1,1-dimethylpyrrolidinium bromide. Its empirical formula is C 19 H 28 BrNO 3 , its molecular weight is 398.33, and its structural formula is: Each 1 mg tablet contains: Glycopyrrolate, USP 1mg Each 2...
- Glyred
- Glyred-M
- Gramcal
- Granisetron - 1 INDICATIONS AND USAGE Sancuso ® (Granisetron Transdermal System) is indicated for the prevention of nausea and vomiting in patients receiving moderately and/or highly emetogenic chemotherapy regimens of up to 5 consecutive days duration. Sancuso is a serotonin -3 (5-HT3) receptor antagonist indicated for the prevention of nausea and vomiting in patients receiving moderately and/or highly...
- Gynergen
- Gyros - Pharmacological action Ofloxacin is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
- HCT - Hydrochlorothiazide information Hydrochlorothiazide is an antihypertensive, diuretic drug that acts on the electrolyte reabsorption in the renal tubular mechanism increasing the excretion of chloride and sodium in equivalent amounts. The exact mechanism of its antihypertensive action is not known at this time. Hydrochlorothiazide indications Hydrochlorothiazide is typically employed for the treatment of patients suffering from hypertension, either as monotherapy or in combination with...
- Haloperidol - WARNING Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7...
- Haloperidol LA
- Hapilux
- Heartburn Relief - Famotidine is known as an H2 histamine blocker. It works by reducing the amount of acid in your stomach . It is used to prevent and treat heartburn and other symptoms caused by too much acid in the stomach (acid indigestion). Check the ingredients on the label even if you have used the product before. The manufacturer may have changed the ingredients. Also, products with similar names may contain different ingredients meant for different purposes. Taking the wrong product could harm you.
- Hedix
- Heparin - Unfractionated heparin (UH) is a heterogenous preparation of anionic, sulfated glycosaminoglycan polymers with weights ranging from 3000 to 30,000 Da. It is a naturally occurring anticoagulant released from mast cells. It binds reversibly to antithrombin III (ATIII) and greatly accelerates the rate at which ATIII inactivates coagulation enzymes thrombin (factor IIa) and factor Xa. UH is different from low molecular weight heparin (LMWH) in the following ways: the average molecular weight of...
- Heparin preservative free
- Hepasol Lipogel
- Herpoviric - Pharmacological action Acyclovir Pharma is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against...
- Hexa-Blok - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Hexa-Defital Lotion
- Hexa-Defital NF
- Hexa-Defital Shampoo
- Hexabotin - Pharmacological action Erythromycin is a macrolide antibiotic. Has bacteriostatic action. However at higher doses against susceptible organisms has a bactericidal effect. erythromycin is reversibly bound to the ribosome of bacteria, thereby inhibiting protein synthesis. Erythromycin is active against gram-positive bacteria: Staphylococcus spp. (strains producing and not producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae); gram-negative bacteria: Neisseria...
- Hexadilat - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Hexaglucon
- Hexalacton - Pharmacological action Spironolactone is a potassium, magnesium sparing diuretic. This medication is a competitive antagonist of aldosterone on the effect on distal nephron (competes for binding sites on cytoplasmic protein receptors, reduces the synthesis of permeases in the aldosterone-sensitive part of collecting tubules and distal tubules), increases the excretion of Na+, Cl- and water and reduces the excretion of K+ and urea, reduces the titratable acidity of urine. Increased diuresis...
- Hexalid
- Hexamet
- Hexamycin
- Hexanurat - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Hexapindol
- Hexaretic
- Hexarone
- Hexasoptin
- Hexazide - Hydrochlorothiazide information Hydrochlorothiazide is an antihypertensive, diuretic drug that acts on the electrolyte reabsorption in the renal tubular mechanism increasing the excretion of chloride and sodium in equivalent amounts. The exact mechanism of its antihypertensive action is not known at this time. Hydrochlorothiazide indications Hydrochlorothiazide is typically employed for the treatment of patients suffering from hypertension, either as monotherapy or in combination with...
- Hiconcil
- Higroton
- Higroton-Res
- Histamed
- Histaterfen
- Hjerdyl
- Hormodausse
- Humanalbumin ZLB
- Hydralazine - A direct-acting vasodilator that is used as an antihypertensive agent. [PubChem] Indication: For the treatment of essential hypertension, alone or as an adjunct. Also for the management of severe hypertension when the drug cannot be given orally or when blood pressure must be lowered immediately, congestive heart failure (in combination with cardiac glycosides and diuretics and/or with isosorbide dinitrate), and hypertension secondary to pre-eclampsia/eclampsia. A vasodilator, hydralazine works...
- Hydrex - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Hydrochloorthiazide - Hydrochlorothiazide information Hydrochlorothiazide is an antihypertensive, diuretic drug that acts on the electrolyte reabsorption in the renal tubular mechanism increasing the excretion of chloride and sodium in equivalent amounts. The exact mechanism of its antihypertensive action is not known at this time. Hydrochlorothiazide indications Hydrochlorothiazide is typically employed for the treatment of patients suffering from hypertension, either as monotherapy or in combination with...
- Hydrochlorothiazide - Hydrochlorothiazide information Hydrochlorothiazide is an antihypertensive, diuretic drug that acts on the electrolyte reabsorption in the renal tubular mechanism increasing the excretion of chloride and sodium in equivalent amounts. The exact mechanism of its antihypertensive action is not known at this time. Hydrochlorothiazide indications Hydrochlorothiazide is typically employed for the treatment of patients suffering from hypertension, either as monotherapy or in combination with...
- Hydromorphone - An opioid analgesic derived from morphine and used mainly as an analgesic. It has a shorter duration of action and is more potent than morphine. [PubChem] Indication: For the relief of moderate to severe pain such as that due to surgery, cancer, trauma/injury, or burns. Hydromorphone is a hydrogenated ketone derivative of morphine that acts as a narcotic analgesic. It has a shorter duration of action than morphine. Hydromorphone is approximately 8 times more potent on a milligram basis than...
- Hydromorphone HP
- Hydromorphone HP Forte
- Hydroxychloroquine - A chemotherapeutic agent that acts against erythrocytic forms of malarial parasites. Indication: For the suppressive treatment and treatment of acute attacks of malaria due to Plasmodium vivax, P. malariae, P. ovale, and susceptible strains of P. falciparum. It is also indicated for the treatment of discoid and systemic lupus erythematosus, and rheumatoid arthritis. Hydroxychloroquine possesses antimalarial properties and also exerts a beneficial effect in lupus erythematosus (chronic discoid...
- Hydroxydes Aluminium / Magnesium Sandoz Conseil
- Hydroxyzine - Hydroxyzine information This medication is made by Pfizer and is generically known as hydroxyzine hydrochloride and is available in tablet and syrup form. Hydroxyzine indications This drug is prescribed for the relief of anxiety and tension brought about by psychoneurosis. Hydroxyzine may also be used for the containment of pruritus due to allergic reactions such as chronic uticaria and contact dermatitis. Hydroxyzine may be used as a sedative when used as a premedication following...
- Hyoscine
- Hypnor
- Hypolar Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- INH-Ciba
- ISDN - Isosorbide dinitrate belongs to the class of medications called anti-anginals . It is used to prevent chest pain associated with angina. It works by relaxing blood vessels and increasing the blood and oxygen supply to the heart. Isosorbide dinitrate may reduce the number, length, and severity of angina attacks. Tolerance for exercise may be increased and the need for fast-acting nitroglycerin (tablets and spray) may be reduced.
- Ibax
- Ibu Eco - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ibuphlogont - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ibuphlogont Retard - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ibuprofen - SPL UNCLASSIFIED SECTION Rx Only Cardiovascular Risk • NSAIDs may cause an increased risk of serious cardiovascular thrombotic events,...
- Ibuprofene - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ibuprofene Conseil - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Ibuprofeno - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Idarubicin - An orally administered anthracycline antineoplastic. The compound has shown activity against breast cancer, lymphomas and leukemias, together with the potential for reduced cardiac toxicity. [PubChem] Indication: For the treatment of acute myeloid leukemia (AML) in adults. This includes French-American-British (FAB) classifications M1 through M7. Idarubicin is an antineoplastic in the anthracycline class. General properties of drugs in this class include: interaction with DNA in a variety of...
- Imadrax
- Imipenem; Cilastatin
- Imipramine - Imipramine, the prototypical tricyclic antidepressant (TCA), is a dibenzazepine-derivative TCA. TCAs are structurally similar to phenothiazines. They contain a tricyclic ring system with an alkyl amine substituent on the central ring. In non-depressed individuals, imipramine does not affect mood or arousal, but may cause sedation. In depressed individuals, imipramine exerts a positive effect on mood. TCAs are potent inhibitors of serotonin and norepinephrine reuptake. Tertiary amine TCAs, such...
- Immunal
- Imozop - Pharmacological action Zopiclone is a sleeping drug from group of cyclopyrrolone derivatives. This drug is "non benzodiazepine" agonist of benzodiazepine receptors. Zopiclone also has sedative, anxiolytic, muscle-relaxing center, anticonvulsant and amnesic properties. Like a derivative of benzodiazepine zopiclone enhances GABA-ergic processes in the brain, interacting with the benzodiazepine receptors, as a result of the increased sensitivity of GABA-receptors to the neurotransmitter....
- Imurek
- Imurek I.V.
- Indapamide - SPL UNCLASSIFIED SECTION 40-9191 Revised — November 2015 Rx Only DESCRIPTION Indapamide is an oral antihypertensive/diuretic. Its molecule contains both a polar sulfamoyl chlorobenzamide moiety and a lipid-soluble methylindoline moiety. It differs...
- Indo-Phlogont
- Indolar SR
- Indometacine
- Indomethacin - SPL UNCLASSIFIED SECTION Rx only ...
- Indomethacin ER
- InfectoTrimet
- Inflacor
- Infufer - Iron dextran belongs to a class of medications known as iron supplements. It is an injectable form of iron that is used to treat iron-deficiency anemia when oral iron supplements cannot be taken or when oral iron supplements have not produced the needed results. Iron is important for the production of red blood cells. It helps red blood cells to carry oxygen to the various parts of the body. Your doctor may have suggested this medication for conditions other than the ones listed in...
- Infuvite Pediatric
- Intemipril - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Introvale - This combination hormone medication is used to prevent pregnancy . It contains 2 hormones: a progestin ( levonorgestrel ) and an estrogen (ethinyl estradiol ). It works mainly by preventing the release of an egg ( ovulation ) during your menstrual cycle. It also makes vaginal fluid thicker to help prevent sperm from reaching an egg (fertilization) and changes the lining of the uterus (womb) to prevent attachment of a fertilized egg. If a fertilized egg does not attach to the uterus, it...
- Invagesic
- Invagesic Forte
- Ipocol
- Iprolan
- Irahex
- Irbesartan - Irbesartan information Irbesartan is a drug that classified as an Angiotensin II receptor antagonist. Irbesartan indications This blood pressure medication (Irbesartan Zydus Pharmaceuticals) is indicated for the treatment of hypertension or high blood pressure. Irbesartan works by preventing the narrowing of blood vessels and arteries and it also prevents the constriction of the flow of blood. Buy Irbesartan Zydus Pharmaceuticals, as it is also prescribed for the treatment of kidney...
- Irbesartan; Hydrochlorothiazide - This drug is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: irbesartan and hydrochlorothiazide . Irbesartan is an angiotensin receptor blocker and works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) that causes you to make more urine, which helps your body get rid of extra salt and water....
- Irenax
- Irinotecan - Irinotecan is an antineoplastic enzyme inhibitor primarily used in the treatment of colorectal cancer. It is a derivative of camptothecin that inhibits the action of topoisomerase I. Irinotecan prevents religation of the DNA strand by binding to topoisomerase I-DNA complex, and causes double-strand DNA breakage and cell death. Indication: For the treatment of metastatic colorectal cancer (first-line therapy when administered with 5-fluorouracil and leucovorin). Also used in combination with...
- Isodur
- Isomonit
- Isomonit Retard
- Isoniazid - SPL UNCLASSIFIED SECTION Rev. 02/11 Rx Only WARNING Severe and sometimes fatal hepatitis associated with isoniazid therapy has been reported and may occur or may develop even after many months of treatment. The risk of developing hepatitis is age related. Approximate case rates by age are: less than 1 per 1,000 for persons under 20 years of age, 3 per 1...
- Isosorbide Dinitrate - SPL UNCLASSIFIED SECTION Rev. 11/10 Rx Only DESCRIPTION Isosorbide dinitrate (ISDN) is 1,4:3,6-dianhydro-D-glucitol 2,5-dinitrate, an organic nitrate whose structural formula is: and whose molecular weight is 236.14. The organic nitrates are vasodilators,...
- Isosorbide Mononitrate - DESCRIPTION monoket ® , an organic nitrate, is a vasodilator with effects on both arteries and veins. The empirical formula is C 6 H 9 NO 6 and the molecular weight is 191.14. The chemical name for monoket ® is 1,4:3,6-Dianhydro-D-glucitol 5-nitrate and the compound has the following structural formula: monoket ® is available in 10 mg and 20 mg tablets. Each tablet also contains as inactive ingredients: ...
- Isosorbidedinitraat Retard
- Isosorbidemononitraat
- Isosorbidemononitraat Retard
- Isostenase
- Isostenase Retard
- Isotretinoin - DO NOT GET PREGNANT CONTRAINDICATIONS AND WARNINGS Isoxsuprine - This medication is used along with other treatment for certain blood vessel diseases (e.g., arteriosclerosis obliterans, Raynaud's disease, Buerger's disease , cerebrovascular insufficiency). It works by widening blood vessels to help increase blood flow (improve circulation) to certain parts of the body (e.g., hands/ feet , brain ). This effect may help to decrease symptoms such as cold hands and feet, numbness, tingling, and decreased memory or judgment.
- Ispagel
- Istret
- Itraconazol
- Itraconazole - WARNING: CONGESTIVE HEART FAILURE, CARDIAC EFFECTS, AND DRUG INTERACTIONS Do not administer ONMEL for the treatment of onychomycosis in patients with evidence of ventricular dysfunction such as congestive heart failure (CHF) or a history of CHF. When itraconazole was administered intravenously to dogs and healthy human volunteers, negative inotropic effects were seen. If signs or symptoms of congestive...
- Ivel Mono
- Josalid
- Justum
- Kafsir
- Kanisar
- Kefotax
- Kefzol - Cefazolin is an antibiotic used to treat a wide variety of bacterial infections . It may also be used before and during certain surgeries to help prevent infection. This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria.
- Kelofibrase
- Ketamine - A cyclohexanone derivative used for induction of anesthesia. Its mechanism of action is not well understood, but ketamine can block NMDA receptors (receptors, N-methyl-D-aspartate) and may interact with sigma receptors. [PubChem] Indication: For use as the sole anesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. Ketamine is a rapid-acting general anesthetic producing an anesthetic state characterized by profound analgesia, normal...
- Ketaxal
- Ketoconazole - WARNING When used orally, ketoconazole has been associated with hepatic toxicity, including some fatalities. Patients receiving this drug should be informed by the physician of the risk and should be closely monitored. See WARNINGS and PRECAUTIONS sections. Coadministration of terfenadine with ketoconazole tablets is contraindicated. Rare cases of serious cardiovascular adverse events, including death, ventricular tachycardia and...
- Ketohexal
- Ketonal - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketoprofen - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketoprofene - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketoprofene GNR - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketoprofene LP - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Ketorolac - A pyrrolizine carboxylic acid derivative structurally related to indomethacin. It is an NSAID and is used principally for its analgesic activity. (From Martindale The Extra Pharmacopoeia, 31st ed) Indication: For the short-term (~5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting. Ketorolac, an antiinflammatory agent with analgesic and antipyretic properties, is used to treat osteoarthritis and control acute pain....
- Ketotifen - Active ingredient Ketotifen (0.025%) (equivalent to ketotifen fumarate 0.035%) Purpose Antihistamine Use Temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander. Warnings Do not use ...
- Klacid HP 7
- Klacid HP7
- Klarmyn
- Klarmyn SR
- Klidibrax
- Kogrel
- Kontagripp - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Kontagripp Mono - Pharmacological action NSAIDs, a derivative of phenylpropionic acid, ibuprofen has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to both peripheral (indirectly, through suppression of prostaglandin synthesis), and a central...
- Kontagripp-RR
- Kuracid
- Kuterid
- L-Arginine - An essential amino acid that is physiologically active in the L-form. [PubChem] Indication: Used for nutritional supplementation, also for treating dietary shortage or imbalance. Studies have shown that is has improved immune responses to bacteria, viruses and tumor cells; promotes wound healing and regeneration of the liver; causes the release of growth hormones; considered crucial for optimal muscle growth and tissue repair.
- Labetalol - Blocker of both alpha- and beta-adrenergic receptors that is used as an antihypertensive. [PubChem] Indication: For the management of hypertension (alone or in combination with other classes of antihypertensive agents), as well as chronic stable angina pectoris and sympathetic overactivity syndrome associated with severe tetanus. Labetalol is used parenterally for immediate reduction in blood pressure in severe hypertension or in hypertensive crises when considered an emergency, for the control...
- Labimion
- Labistatin - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Lactulose - DESCRIPTION Lactulose is a synthetic disaccharide in solution form for oral administration. Each 15 mL of Lactulose Solution contains: 10 g lactulose (and less than 1.6 g galactose, less than 1.2 g lactose, and 1.2 g or less of other sugars). Also contains FD&C Yellow No. 6, purified water, and flavoring. Sodium hydroxide used to adjust pH . The pH range is 2.5 to 6.5. Lactulose is a colonic acidifier which promotes laxation. The...
- Lactulosestroop
- Lakea
- Lameton
- Lamotrigin
- Lamotrigine - WARNING: SERIOUS SKIN RASHES See full prescribing information for complete boxed warning. Cases of life-threatening serious rashes, including Stevens-Johnson syndrome and toxic...
- Lansoprazol
- Lansoprazole - Active ingredient (in each capsule) Lansoprazole 15 mg Purpose Acid reducer Use • treats frequent heartburn (occurs 2 or more days a week) • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full...
- Larafen - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Larapam
- Lectrum
- Leflunomide - Leflunomide information This medication, with the generic name of Leflunomide, is specially formulated to provide physical relief from inflammation, swelling, stiffness, and joint pain as caused by rheumatoid arthritis. Leflunomide acts by stopping the production of too much immune cells causing inflammation and swelling in the body. Leflunomide indications Leflunomide is prescribed to patients showing signs of rheumatism as listed below: Inflammation Swelling Stiffness Joint pain ...
- Lesifit
- Leucovorin - The active metabolite of folic acid. Leucovorin is used principally as its calcium salt as an antidote to folic acid antagonists which block the conversion of folic acid to folinic acid. [PubChem] Indication: For the treatment of osteosarcoma (after high dose methotrexate therapy). Used to diminish the toxicity and counteract the effects of impaired methotrexate elimination and of inadvertent overdosages of folic acid antagonists, and to treat megaloblastic anemias due to folic acid deficiency....
- Leucovorine
- Leuprolide - Leuprolide is used to treat advanced prostate cancer in men. It is not a cure. Most types of prostate cancer need the male hormone testosterone to grow and spread. Leuprolide works by reducing the amount of testosterone that the body makes. This helps slow or stop the growth of cancer cells and helps relieve symptoms such as painful/difficult urination. Talk to your doctor about the risks and benefits of treatment. OTHER USES: This section contains uses of this drug that are not...
- Leuprorelin 1 Monat
- Leuprorelin 3 Monate
- Levetiracetam - Levetiracetam information Levetiracetam is type of drug that belongs to the group of medicines called antiepileptic drug. Levetiracetam indications This medication is indicated to control seizure. The precise way of how Levetiracetam works is not yet known. This medicine may also be used for purposes not mentioned here. Levetiracetam warnings This drug belongs in the FDA pregnancy category C. Levetiracetam may cause severe side effects to an unborn baby. Do not take Levetiracetam...
- Levhexal
- Levodopa-Carbi
- Levofloxacin - Indications and Usage Plague (1.14) 04/2012 Dosage and Administration Dosage in Adult Patients with Normal Renal Function (2.1) 04/2012 Dosage in Pediatric Patients (2.2) ...
- Levothyroxine - The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (monoiodotyrosine) and the coupling of iodotyrosines (diiodotyrosine) in the thyroglobulin. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form triiodothyronine which exerts a broad spectrum of stimulatory effects on cell metabolism. [PubChem] Indication: For use alone or in combination with antithyroid agents...
- Levoxal
- Lictyn
- Lidocaine; Prilocaine
- Lidomyxin
- Linatil
- Linatil Comp
- Linatil Comp Mite
- Linbac
- Lindacil
- Lindynette
- Linex
- Linoxal - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Lisdene - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Lisinopril - WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue lisinopril as soon as possible [see Warnings and Precautions (5.1) ]. • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see ...
- Lisinopril HCT
- Lisinopril HCTZ
- Lisinopril-BC - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Lisinopril; Hydrochlorothiazide - This medication is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: lisinopril and hydrochlorothiazide . Lisinopril is an ACE inhibitor and works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) that causes you to make more urine, which helps your body get rid of extra salt and water. This...
- Lisinopril; Hydrochlorthiazid
- Lisitril - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Lisitril Comp.
- Lisobac
- Listril - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Listril Comp
- Lo-Tone
- Lo-Uric - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Locasalen
- Lodiric - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Lomilan
- Lomilan Express
- Lonox - This medication is used to treat diarrhea . It helps to decrease the number and frequency of bowel movements. It works by slowing the movement of the intestines . Diphenoxylate is similar to narcotic pain relievers, but it acts mainly to slow the gut. Atropine belongs to a class of drugs known as anticholinergics, which help to dry up body fluids and also slow gut movement.
- Lopedium
- Lopedium Express
- Lopedium ISO
- Lopedium T
- Loperamid
- Loperamide - One of the long-acting synthetic antidiarrheals; it is not significantly absorbed from the gut, and has no effect on the adrenergic system or central nervous system, but may antagonize histamine and interfere with acetylcholine release locally. [PubChem] Indication: For the control and symptomatic relief of acute nonspecific diarrhea and of chronic diarrhea associated with inflammatory bowel disease or gastroenteritis. Also used for reducing the volume of discharge from ileostomies. Loperamide...
- Loperamide Conseil
- Loperamide Viaref
- Loperol
- Lopimed
- Lopresor - Metoprolol belongs to the class of medications called beta-blockers. Metoprolol is used to treat high blood pressure and prevent the symptoms of angina (chest pain). It is also used to help reduce the risk of death right after a heart attack. It works by reducing the demands put on the heart. Metoprolol is also taken by people who have had a heart attack to reduce the risk of having another one. Metoprolol is often used in combination with other high blood pressure medications such as...
- Lopresor Retard
- Lopresor-R
- Lorado
- Lorado Pollen
- Lorano
- Lorano Akut
- Loratadin
- Loratadina
- Loratadine - Active ingredient (in each tablet) Loratadine 10 mg Purpose Antihistamine Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • itchy, watery eyes ...
- Loratin Express
- Lorazepam - DESCRIPTION Each mL of Lorazepam Concentrate, USP for oral administration contains: Lorazepam . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 mg Inactive Ingredients Lorazepam Oral Concentrate, USP contains polyethylene glycol, propylene glycol and triacetin. Lorazepam, an antianxiety agent, has the chemical formula, ...
- Loromycin - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
- Loryna - This medication is a combination of 2 hormones: an estrogen (ethinyl estradiol ) and a progestin (drospirenone). This product is used to prevent pregnancy . It works mainly by preventing the release of an egg ( ovulation ) during your menstrual cycle. It also makes vaginal fluid thicker to help prevent sperm from reaching an egg (fertilization) and changes the lining of the uterus (womb) to prevent attachment of a fertilized egg. If a fertilized egg does not attach to the uterus, it...
- Losartan - Losartan is an angiotensin-receptor blocker (ARB) that may be used alone or with other agents to treat hypertension. Losartan and its longer acting metabolite, E-3174, lower blood pressure by antagonizing the renin-angiotensin-aldosterone system (RAAS); they compete with angiotensin II for binding to the type-1 angiotensin II receptor (AT1) subtype and prevents the blood pressure increasing effects of angiotensin II. Unlike angiotensin-converting enzyme (ACE) inhibitors, ARBs do not have the...
- Losartan; Hydrochlorothiazide - This drug is used to treat high blood pressure . It is also used to lower the risk of strokes in patients with high blood pressure and an enlarged heart . Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains two medications: losartan and hydrochlorothiazide . Losartan is an angiotensin receptor blocker and works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) that...
- Lotensin Hctz
- Lovastatin - DESCRIPTION Lovastatin, USP is a cholesterol lowering agent isolated from a strain of Aspergillus terreus . After oral ingestion, lovastatin, USP, which is an inactive lactone, is hydrolyzed to the corresponding β-hydroxyacid form. This is a principal metabolite and an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase. This enzyme catalyzes the conversion of HMG-CoA to mevalonate, which is an early and rate limiting step in the...
- Lovastatina
- Loxapac
- Loxapac IM - Loxapine belongs to the class of medications called antipsychotics . It is used to treat the symptoms of schizophrenia. This medication is believed to work by changing the way that certain nerve signals work in the brain. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed this with your doctor or...
- MCP
- Macalvit
- Macalvit Effervescent
- Macalvit Injections
- Macalvit Orange
- Macalvit Zitrone
- Magluphen
- Magnesium
- Magnesium Forte
- Magnesium Sandoz Eco
- Magnesium Sandoz Forte
- Magnesium Sandoz Quick Minerals
- Magnesium Sulfate - SPL UNCLASSIFIED SECTION Magnesium Sulfate Injection, USP Ansyr™ Plastic Syringe Rx...
- Malex - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Malonetta
- Mandolgin - Pharmacological action Tramadol Karnataka Antibiotics & Pharmaceuticals is an opioid analgesic, a derivative of cyclohexanol. It is non-selective agonist of mu-, delta- and kappa-receptors in the CNS. Tramadol is a racemate (+) and (-) of isomers (50% / 50%) which in various ways are involved in analgesic effects. The isomer (+) is a pure agonist opioid receptors, it has low tropism and has a pronounced selectivity for different subtypes of receptors. The isomer (-) inhibiting neuronal...
- Mandolgin Retard - Pharmacological action Tramadol Karnataka Antibiotics & Pharmaceuticals is an opioid analgesic, a derivative of cyclohexanol. It is non-selective agonist of mu-, delta- and kappa-receptors in the CNS. Tramadol is a racemate (+) and (-) of isomers (50% / 50%) which in various ways are involved in analgesic effects. The isomer (+) is a pure agonist opioid receptors, it has low tropism and has a pronounced selectivity for different subtypes of receptors. The isomer (-) inhibiting neuronal...
- Mandolgin Uno - Pharmacological action Tramadol Karnataka Antibiotics & Pharmaceuticals is an opioid analgesic, a derivative of cyclohexanol. It is non-selective agonist of mu-, delta- and kappa-receptors in the CNS. Tramadol is a racemate (+) and (-) of isomers (50% / 50%) which in various ways are involved in analgesic effects. The isomer (+) is a pure agonist opioid receptors, it has low tropism and has a pronounced selectivity for different subtypes of receptors. The isomer (-) inhibiting neuronal...
- Mantus
- Maprotiline - Maprotiline is a tetracyclic antidepressant with similar pharmacological properties to tricyclic antidepressants (TCAs). Similar to TCAs, maprotiline inhibits neuronal norepinephrine reuptake, possesses some anticholinergic activity, and does not affect monoamine oxidase activity. It differs from TCAs in that it does not appear to block serotonin reuptake. Maprotiline may be used to treat depressive affective disorders, including dysthymic disorder (depressive neurosis) and major depressive...
- Masulin
- Maxamox
- Mebendazol - Pharmacological action Mebendazole is a worming medication a broad spectrum of action, it is most effective when enterobioze. This drug causes irreversible disturbance of glucose utilization in the body of the worm and inhibits the synthesis of ATP. Pharmacokinetics Mebendazole is practically not absorbed from the gastrointestinal tract. The plasma protein binding is 90%. This medication is distributed unevenly in organs and accumulates in adipose tissue, liver, and larvae of helminths...
- Meclizine - DESCRIPTION Chemically, meclizine HCl, USP is 1-( p -chloro-α-phenylbenzyl)-4-( m -methylbenzyl) piperazine dihydrochloride monohydrate. Inactive ingredients for the tablets are: colloidal silicon dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate and talc. The 12.5 mg tablets also contain FD&C Blue #1 Aluminum Lake. The 25 mg...
- Meclofenamate
- Medigel
- Medroxyprogesterone - (6 alpha)-17-Hydroxy-6-methylpregn-4-ene-3,20-dione. A synthetic progestational hormone used in veterinary practice as an estrus regulator. [PubChem] Indication: Used as a contraceptive and to treat secondary amenorrhea, abnormal uterine bleeding, pain associated with endometriosis, endometrial and renal cell carcinomas, paraphilia in males, GnRH-dependent forms of precocious puberty, as well as to prevent endometrial changes associated with estrogens. Medroxyprogesterone is a synthetic...
- Mefalgic
- Mefenaminsaure
- Mefloquine - A phospholipid-interacting antimalarial drug (antimalarials). It is very effective against plasmodium falciparum with very few side effects. [PubChem] Indication: For the treatment of mild to moderate acute malaria caused by Mefloquineuine-susceptible strains of Plasmodium falciparum (both chloroquine-susceptible and resistant strains) or by Plasmodium vivax. Also for the prophylaxis of Plasmodium falciparum and Plasmodium vivax malaria infections, including prophylaxis of...
- Megion
- Megion I.M.
- Megion I.V.
- Meglubet
- Meglucon
- Melhexal
- Mellaril
- Melleretten Solution
- Meloxicam - WARNING: RISK OF SERIOUS CARDIOVASCULAR and GASTROINTESTINAL EVENTS Cardiovascular Risk Nonsteroidal anti-inflammatory drugs (NSAIDs) may cause an increased risk of serious cardiovascular (CV) thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may increase with duration of use....
- Meprobamate - C-IV DESCRIPTION Meprobamate is a white powder with a characteristic odor and a bitter taste. It is slightly soluble in water, freely soluble in acetone and alcohol, and sparingly soluble in ether. The structural formula of meprobamate is: ...
- Meritene
- Meropenem - 1 INDICATIONS AND USAGE MERREM IV is a penem antibacterial indicated for the treatment of: • Complicated skin and skin structure infections (adult patients and pediatric patients 3 months of age and older only). (1.1) • Complicated intra-abdominal infections (adult and...
- Mesactol
- Mesalazine - An anti-inflammatory agent, structurally related to the salicylates, which is active in inflammatory bowel disease. It is considered to be the active moiety of sulphasalazine. (From Martindale, The Extra Pharmacopoeia, 30th ed) Indication: For the treatment of active ulcerative proctitis. Mesalazine (INN, BAN), also known as Mesalamine (USAN) or 5-aminosalicylic acid (5-ASA), is an anti-inflammatory drug used to treat inflammation of the digestive tract (Crohn's disease) and mild to moderate...
- Mesantoin
- Metaxalone - DESCRIPTION Metaxalone tablets, USP are available as 400 mg round, peach colored tablets. Chemically, metaxalone is 5-[(3,5- dimethylphenoxy) methyl]-2-oxazolidinone. The empirical formula is C 12 H 15 NO 3 , which corresponds to a molecular weight of 221.25. The structural formula is: Metaxalone, USP is a white to almost white, odorless crystalline powder freely...
- Metfin
- Metformin - Metformin is a biguanide antihyperglycemic agent used for treating non-insulin-dependent diabetes mellitus (NIDDM). It improves glycemic control by decreasing hepatic glucose production, decreasing glucose absorption and increasing insulin-mediated glucose uptake. Metformin is the only oral antihyperglycemic agent that is not associated with weight gain. Metformin may induce weight loss and is the drug of choice for obese NIDDM patients. When used alone, metformin does not cause hypoglycemia;...
- Metformin ER
- Metformin-BC
- Metformina
- Metformine
- Methazolamide - DESCRIPTION: Methazolamide, a sulfonamide derivative, is a white crystalline powder, weakly acidic, slightly soluble in water, alcohol and acetone. The chemical name for methazolamide is: N-[5-(aminosulfonyl)-3-methyl-1,3,4-thiadiazol-2(3H)-ylidene]-acetamide and it has the following structural formula: Each tablet, for oral administration, contains 25 mg or 50 mg methazolamide. In addition, each tablet...
- Methergin
- Methimazole - DESCRIPTION TAPAZOLE ® (Methimazole Tablets, USP) (1-methylimidazole-2-thiol) is a white, crystalline substance that is freely soluble in water. It differs chemically from the drugs of the thiouracil series primarily because it has a 5- instead of a 6-membered ring. Each tablet contains 5 or 10 mg (43.8 or 87.6 µmol) methimazole, an orally administered antithyroid drug. Each tablet also contains lactose monohydrate,...
- Methionin
- Methocarbamol - SPL UNCLASSIFIED SECTION METHOCARBAMOL TABLETS, USP Rev. 03/11 Rx Only DESCRIPTION: Methocarbamol Tablets, USP, a carbamate derivative of guaifenesin, are a central nervous system (CNS) depressant with sedative and musculoskeletal relaxant...
- Methotrexaat
- Methoxsalen - SPL UNCLASSIFIED SECTION CAUTION: METHOXSALEN IS A POTENT DRUG. READ ENTIRE BROCHURE PRIOR TO PRESCRIBING OR DISPENSING THIS MEDICATION. Methoxsalen with UV radiation should be used only by physicians who have special competence in the diagnosis and treatment of psoriasis and who have special training and experience in photochemotherapy. The use of Psoralen and ultraviolet radiation therapy should be under...
- Methyclothiazide - DESCRIPTION Methyclothiazide, a diuretic-antihypertensive agent, is a member of the benzothiadiazine (thiazide) class of drugs. It is an analogue of hydrochlorothiazide and occurs as a white to practically white crystalline powder which is basically odorless. Methyclothiazide is very slightly soluble in water and chloroform, and slightly soluble in alcohol. Chemically, methyclothiazide is represented as 6-chloro-3-(chloromethyl)-3,4-dihydro-2-methyl-2H-1,2...
- Methyldopa - DESCRIPTION Methyldopa is an antihypertensive and is the L-isomer of alpha-methyldopa. It is levo-3-(3,4-dihydroxyphenyl)-2-methylalanine sesquihydrate. Methyldopa is supplied as tablets for oral administration, containing 250 mg and 500 mg of methyldopa. The amount of methyldopa is calculated on the anhydrous basis. Its molecular formula is C 10 H 13 NO 4 •1 1/2 H 2 O, with a molecular weight of 238.24, and its structural formula is: ...
- Methyldopa; Hydrochlorothiazide - This medication is used to treat high blood pressure ( hypertension ). Lowering high blood pressure helps prevent strokes, heart attacks , and kidney problems. This product contains 2 medications: methyldopa and hydrochlorothiazide . Methyldopa works by relaxing blood vessels so blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic). It increases the amount of urine you make, especially when you first start the medication. It also helps to relax the blood...
- Methylene Blue - WARNING: SEROTONIN SYNDROME WITH CONCOMITANT USE OF SEROTONERGIC DRUGS PROVAYBLUE™ may cause serious or fatal serotonergic syndrome when used in combination with serotonergic drugs. Avoid concomitant use of PROVAYBLUE™ with selective serotonin reuptake inhibitors (SSRIs), serotonin and norepinephrine reuptake inhibitors (SNRIs), and monoamine oxidase inhibitors ( 5.1 , ...
- Methylfenidaat
- Methylphenidate - WARNING: ABUSE AND DEPENDENCE CNS stimulants, including COTEMPLA XR-ODT, other methylphenidate-containing products, and amphetamines, have a high potential for abuse and dependence. Assess the risk of abuse prior to prescribing, and monitor for signs of abuse and dependence while on therapy [see Warnings and Precautions (5.1) , Drug Abuse and Dependence (9.2 , 9.3) ] . ...
- Methylphenidate SR
- Methylprednisolone - DESCRIPTION Methylprednisolone Tablets contain methylprednisolone which is a glucocorticoid. Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. Methylprednisolone occurs as a white to practically white, odorless, crystalline powder. It is sparingly soluble in alcohol, in dioxane, and in methanol, slightly soluble in acetone, and in chloroform, and very slightly...
- Meto Zerok
- Metoclopramide - Boxed Warning 8/2017 Indications and Usage ( 1 ) 8/2017 Dosage and Administration, Dosage for Gastroesophageal Reflux ( 2.2 ) 8/2017 Dosage and Administration, Dosage for Acute and...
- Metohexal
- Metolazone - SPL UNCLASSIFIED SECTION Rx Only DO NOT INTERCHANGE ZAROXOLYN TABLETS AND OTHER FORMULATIONS OF METOLAZONE THAT SHARE ITS SLOW AND INCOMPLETE BIOAVAILABILITY AND ARE THERAPEUTICALLY EQUIVALENT AT THE SAME DOSES TO MYKROX® TABLETS, A MORE RAPIDLY AVAILABLE AND COMPLETELY BIOAVAILABLE METOLAZONE PRODUCT. FORMULATIONS BIOEQUIVALENT TO ZAROXOLYN AND FORMULATIONS BIOEQUIVALENT TO MYKROX SHOULD BE INTERCHANGED FOR ONE...
- Metopress
- Metopress Retard
- Metoprolol - Pharmacological action Metoprolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic effect. Metoprolol decreases automaticity of sinus node, reducing heart rate, slows AV-conduction, decreases myocardial contractility and excitability, reduces cardiac output, reduces myocardial oxygen demand. This drug inhibits the stimulatory effect of catecholamines on the heart during physical and...
- Metoprolol ER
- Metoprolol GEA Retard
- Metoprololsuccinaat HCT
- Metoprololsuccinaat Retard
- Metoprololtartraat
- Metoxim
- Metrolyl - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
- Metronidazol - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
- Metronidazole - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
- Mexiletine - Antiarrhythmic agent pharmacologically similar to lidocaine. It may have some anticonvulsant properties. [PubChem] Indication: For the treatment of ventricular tachycardia and symptomatic premature ventricular beats, and prevention of ventricular fibrillation. Mexiletine is a local anesthetic, antiarrhythmic agent (Class Ib), structurally similar to lidocaine, but orally active. Mexiletine has fast onset and offset kinetics, meaning that they have little or no effect at slower heart rates, and...
- Mianserine
- Micocept
- Miconazol
- Miconazol Hydroc
- Miconazolnitraat
- Micozol
- Micro Mn
- Midacum
- Midazolam - A short-acting hypnotic-sedative drug with anxiolytic and amnestic properties. It is used in dentistry, cardiac surgery, endoscopic procedures, as preanesthetic medication, and as an adjunct to local anesthesia. The short duration and cardiorespiratory stability makes it useful in poor-risk, elderly, and cardiac patients. It is water-soluble at pH less than 4 and lipid-soluble at physiological pH. [PubChem] Midazolam is a schedule IV drug in the United States. Indication: For use as a sedative...
- Midazolam-BC
- Midodrine - An ethanolamine derivative that is an adrenergic alpha agonist. It is used as a vasoconstrictor agent in the treatment of hypotension. [PubChem] Indication: For the treatment of symptomatic orthostatic hypotension (OH). Midodrine is a prodrug, i.e., the therapeutic effect of orally administered midodrine is due to the major metabolite desglymidodrine formed by deglycination of midodrine. Desglymidodrine diffuses poorly across the blood-brain barrier, and is therefore not associated with effects...
- Midrat
- Milador
- Milligest
- Milrinone - A positive inotropic cardiotonic agent with vasodilator properties. It inhibits cAMP phosphodiesterase activity in myocardium and vascular smooth muscle. Milrinone is a derivative of amrinone and has 20-30 times the ionotropic potency of amrinone. [PubChem] Indication: Indicated for the treatment of congestive heart failure. Milrinone, a synthetic dimethylxanthine derivative structurally related to theophylline and caffeine, is used in the treatment of peripheral vascular diseases and in the...
- Minocycline - Minocycline information Minocycline belongs to the group tetracycline, which is used to treat infections caused by bacteria. Minocycline works by interfering with the ability of the bacteria to produce proteins, which is very essential to the growth and increase of numbers to the bacteria. Minocycline stops the spread of infection and the remaining bacteria are killed by the immune system or eventually die. Minocycline indications Minocycline is indicated for the treatment different...
- Minotabs
- Minoxidil - Pharmacological action Minoxidil is a drugs for the treatment of hair loss. This medication has a stimulating effect on hair growth in men and women with androgenetic alopecia (male pattern baldness). The appearance of signs of hair growth observed after 4 months or more of taking the drug 2 times / day. The beginning and the severity of the effect may vary in different patients. After the abolition of minoxidil new hair growth stops, and after 3-4 months may restore the original...
- Minoxidil Conseil - Pharmacological action Minoxidil is a drugs for the treatment of hair loss. This medication has a stimulating effect on hair growth in men and women with androgenetic alopecia (male pattern baldness). The appearance of signs of hair growth observed after 4 months or more of taking the drug 2 times / day. The beginning and the severity of the effect may vary in different patients. After the abolition of minoxidil new hair growth stops, and after 3-4 months may restore the original...
- Mirtazapin
- Mirtazapine - Suicidality and Antidepressant Drugs Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of major depressive disorder (MDD) and other psychiatric disorders. Anyone considering the use of mirtazapine tablets or any other antidepressant in a child, adolescent, or young adult must balance this risk with...
- Mirtazipine
- Mirzalux
- Mitoxantron - Mitoxantrone is used to treat leukemia and other cancers. It is also used to treat multiple sclerosis. It belongs to a class of drugs known as anthracenediones and works by slowing or stopping the growth of certain cells (including cancer cells and cells that affect the body's natural defenses).
- Moclo A
- Moclobemide - A reversible monoamine oxidase inhibitor (MAOI) selective for isoform A (RIMA) used to treat major depressive disorder. Indication: For the treatment of depression. Moclobemide belongs to a class of MAOI antidepressants known as reversible inhibitors of monoamine oxidase type-A (RIMAs). The primary role of monoamine oxidase MAO lies in the metabolism of and regulation of the levels of monoamines (serotonin, norepinephrine, and dopamine). Within neurons, MAO appears to regulate the levels of...
- Modisal
- Mogetic
- Mometasone - Mometasone is a medium-potency synthetic corticosteroid with antiinflammatory, antipruritic, and vasoconstrictive properties. Studies in asthmatic patients have demonstrated that mometasone provides a favorable ratio of topical to systemic activity due to its primary local effect along with the extensive hepatic metabolism and the lack of active metabolites. Though effective for the treatment of asthma, glucocorticoids do not affect asthma symptoms immediately. Maximum improvement in symptoms...
- Mondus
- Mononitrato de Isosorbida
- Monostenase
- Monostenase Long
- Monovent
- Morph
- Morphine - DESCRIPTION Opium Tincture, USP (Deodorized), is for oral administration. It is freed from unpleasant odor or nauseating substances by “denarcotization” with a petroleum distillate. Opium tincture is a clear, reddish-brown hydroalcoholic solution. Each 100 mL contains 1 g of anhydrous morphine (represents the equivalent of 10 g of Powdered Opium, USP), alcohol, 19%, and water. Opium has a very characteristic odor and...
- Morphine HP
- Morphine LP Epidural
- Motiron
- Mucolysin
- Multivitamine
- Mycohexal - Pharmacological action Clotrimazole is an antifungal agent of imidazole derivatives group for topical use. This medication has an effect at the expense of the synthesis of ergosterol, which is part of the cell membrane of fungi. Clotrimazole has a broad spectrum of action. Clotrimazole is active against dermatophytes, molds, fungi of the genus Candida, Malassezia furfur. This drug is also active against Corynebacterium minutissimum, Streptococcus spp., Staphylococcus spp., Trichomonas...
- Mycophenolate
- Mycrol
- NAC
- NAC Sandoz Hustenloser
- NGLong
- Nabumetone - SPL UNCLASSIFIED SECTION Rx Only Cardiovascular Risk NSAIDs Through out this package insert, the term NSAID refers to a non-aspirin non-steroidal anti-inflammatory drug. may cause an increased risk of serious cardiovascular thrombotic events,...
- Nadolol - DESCRIPTION Nadolol is a synthetic nonselective beta-adrenergic receptor blocking agent designated chemically as 1-( tert -butylamino)-3-[(5, 6, 7, 8-tetrahydro- cis -6, 7-dihydroxy-1-naphthyl)oxy]-2-propanol. Structural formula: C 17 H 27 NO 4 M.W. 309.40 Nadolol is a white crystalline powder. It is freely soluble in ethanol, soluble in hydrochloric acid, slightly soluble in...
- Nafcillin - SPL UNCLASSIFIED SECTION For Intramuscular or Intravenous Injection To reduce the development of drug-resistant bacteria and maintain the effectiveness of Nafcillin for Injection and other antibacterial drugs, Nafcillin for Injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Nakom
- Nakom Mite
- Naloxone - A specific opiate antagonist that has no agonist activity. It is a competitive antagonist at mu, delta, and kappa opioid receptors. [PubChem] Indication: For the complete or partial reversal of narcotic depression, including respiratory depression, induced by opioids including natural and synthetic narcotics, propoxyphene, methadone and the narcotic-antagonist analgesics: nalbuphine, pentazocine and butorphanol. Naloxone is an opiate antagonist and prevents or reverses the effects of opioids...
- Naltrexon
- Naltrexone - Dosage and Administration, Directions for Use ( 2.4 ) x/2015 ...
- Naproxen - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Naproxen DR - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Naproxen EC - Naproxen EC information Naproxen EC is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen EC Sanis Health's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen EC indications Naproxen EC is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation...
- Naproxennatrium
- Naratriptan - Naratriptan is a triptan drug used for the treatment of migraine headaches. It is a selective 5-hydroxytryptamine1 receptor subtype agonist. Indication: For the acute treatment of migraine attacks with or without aura in adults. Naratriptan is a selective agonist of serotonin (5-hydroxytryptamine; 5-HT) type 1B and 1D receptors. It is structurally and pharmacologically related to other selective 5-HT1B/1D receptor agonist. Naratriptan has only a weak affinity for 5-HT1A, 5-HT5A, and 5-HT7...
- Nasal Drops - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- NasenSpray
- Natriumcromoglicaat
- Natriumvalproaat
- Natriumvalproaat Chrono
- Nauseatol - Dimenhydrinate belongs to a group of medications called antiemetics. This medication is used to prevent and treat motion sickness as well as nausea and vomiting associated with various conditions such as chemotherapy, radiation, and surgery. It is also used to treat nausea and spinning sensations ( vertigo ) due to Ménière's disease and other conditions that cause these symptoms. Dimenhydrinate works to relieve or prevent nausea and vomiting by affecting the vomiting centre...
- Naxen - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Nebacetin
- Nefazodone - Nefazodone hydrochloride (trade name Serzone) is an antidepressant drug marketed by Bristol-Myers Squibb. Its sale was discontinued in 2003 in some countries, due to the small possibility of hepatic (liver) injury, which could lead to the need for a liver transplant, or even death. The incidence of severe liver damage is approximately 1 in 250,000 to 300,000 patient-years. On May 20, 2004, Bristol-Myers Squibb discontinued the sale of Serzone in the United States. [Wikipedia] Indication: For...
- Neo Citran Daycaps
- Neo Citran Extra Strength
- NeoCitran - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Neocitec
- Neostigmine - A cholinesterase inhibitor used in the treatment of myasthenia gravis and to reverse the effects of muscle relaxants such as gallamine and tubocurarine. Neostigmine, unlike physostigmine, does not cross the blood-brain barrier. [PubChem] Indication: Neostigmine is used for the symptomatic treatment of myasthenia gravis by improving muscle tone. Neostigmine is a cholinesterase inhibitor used in the treatment of myasthenia gravis and to reverse the effects of muscle relaxants such as gallamine...
- Neurolep
- Neurolep LC
- Neurospas - Pharmacological action Baclofen is a centrally acting muscle relaxant; GABA B -receptor agonist. It depresses mono-and polysynaptic reflexes presumably by reducing the release of excitatory amino acids (glutamate and aspartate) from the terminals which occurs as a result of stimulation of presynaptic GABA-receptors. This medication does not affect the transmission of impulses in the nerve-muscle synapses; reduces skeletal muscle tone; has a moderate analgesic effect. Pharmacokinetics ...
- Neurozepam
- Neutrilac
- Niacin - DESCRIPTION Niacin or nicotinic acid, a water-soluble B-complex vitamin and antihyperlipidemic agent, is 3-pyridinecarboxylic acid. It is a white, crystalline powder, sparingly soluble in water. It has the following structural formula: Each NIACOR ® Tablet, for oral administration, contains 500 mg of nicotinic acid. In addition, each tablet contains the following inactive ingredients: croscarmellose sodium, hydrogenated...
- Nif-Atenil
- Nife-Basan - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nife-Basan CR - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nife-Basan Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifecard XL - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedalat - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipat - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipat Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipat Uno - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipin CR - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipine - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipine LP - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifedipine Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifehexal Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nifidine - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
- Nimadorm
- Nitrazepam - A benzodiazepine derivative used as an anticonvulsant and hypnotic. Indication: Used to treat short-term sleeping problems (insomnia), such as difficulty falling asleep, frequent awakenings during the night, and early-morning awakening. Nitrazepam is a type of benzodiazepine drug. It is a powerful hypnotic drug which possesses strong sedative, anxiolytic, amnestic, anticonvulsant, and skeletal muscle relaxant properties. Nitrazepam shortens the time required to fall asleep and lengthens the...
- Nitrendepat
- Nitrofurantoin - SPL UNCLASSIFIED SECTION (Twice-a-day Dosage) Rx Only SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of nitrofurantoin capsules USP (monohydrate/macrocrystals) and other antibacterial drugs, nitrofurantoin capsules USP (monohydrate/macrocrystals) should be used only to treat or prevent...
- Nitroglycerin - SPL UNCLASSIFIED SECTION Rx DESCRIPTION: Molecular Structure Structural Formula SPL UNCLASSIFIED SECTION Molecular Structure ...
- Nitroglycerin SR
- Nitroglycerine
- Nizatidine - SPL UNCLASSIFIED SECTION Rx Only DESCRIPTION Nizatidine, USP is a histamine H2-receptor antagonist. Chemically, it is N -[2-[[[2-[(dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]- N’ -methyl-2-nitro-1,1-ethenediamine. The structural formula is as follows: Nizatidine, USP has the empirical...
- Nopyn
- NorLevo
- NorLevo Uno
- Noranat
- Norepinephrine - Precursor of epinephrine that is secreted by the adrenal medulla and is a widespread central and autonomic neurotransmitter. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers and of the diffuse projection system in the brain arising from the locus ceruleus. It is also found in plants and is used pharmacologically as a sympathomimetic. [PubChem] Indication: Mainly used to treat patients in vasodilatory shock states such as septic shock and neurogenic shock and...
- Norethisterone
- Norflox
- Norfloxacin - A synthetic fluoroquinolone (fluoroquinolones) with broad-spectrum antibacterial activity against most gram-negative and gram-positive bacteria. Norfloxacin inhibits bacterial DNA gyrase. [PubChem] Indication: For the treatment of urinary tract infection Norfloxacin is a quinolone/fluoroquinolone antibiotic. Norfloxacin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase, which allows the untwisting required to...
- Norfloxacine
- Norfloxacino
- Norsol
- Nortriptyline - Nortriptyline hydrochloride, the N-demethylated active metabolite of amitriptyline, is a dibenzocycloheptene-derivative tricyclic antidepressant (TCA). TCAs are structurally similar to phenothiazines. They contain a tricyclic ring system with an alkyl amine substituent on the central ring. In non-depressed individuals, nortriptyline does not affect mood or arousal, but may cause sedation. In depressed individuals, nortriptyline exerts a positive effect on mood. TCAs are potent inhibitors of...
- Novo Fosfostilben
- Novynette
- Nubain
- Nubrex
- Nydrazid
- Nystatin - DESCRIPTION Nystatin, USP is an antimycotic polyene antibiotic obtained from Streptomyces noursei . Its structural formula: C 47 H 75 NO 17 M.W. 926.13 Nystatin Tablets USP contain the inactive ingredients: Corn Starch, Povidone, Compressible Sugar, Microcrystalline Cellulose, Sodium Starch Glycolate, Talc, Magnesium Stearate,...
- Odemase - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Odemase Retard - Pharmacological action Furosemide is a loop diuretic. This medication violates the reabsorption of sodium and chlorine in the large segment of the ascending loop of Henle. Due to increasing separation of sodium ions occurs secondary (indirect osmotically bound water) increased excretion of water and increased secretion of potassium ions in the distal renal tubule. Simultaneously increased excretion of calcium and magnesium ions. Furosemide has secondary effects caused by the release of...
- Odemo-Genat
- Oflox - Pharmacological action Ofloxacin is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
- Ofloxacin - Pharmacological action Ofloxacin is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
- Ofloxacine - Pharmacological action Ofloxacin is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
- Oksibutin
- Olandoz
- Olmesartan - Olmesartan is an antihypertensive agent which belongs to the class of medicines called angiotensin II receptor antagonists. It acts rapidly to lower high blood pressure. It is marketed worldwide by Daiichi Sankyo, Ltd. and in the United States by Daiichi Sankyo, Inc. and Forest Laboratories. Indication: For the treatment of hypertension. Olmesartan, a specific angiotensin II type 1 antagonist, is used alone or with other antihypertensive agents to treat hypertension. Unlike the angiotensin...
- Olopatadine - Used to treat allergic conjunctivitis (itching eyes), olopatadine inhibits the release of histamine from mast cells. It is a relatively selective histamine H1 antagonist that inhibits the in vivo and in vitro type 1 immediate hypersensitivity reaction including inhibition of histamine induced effects on human conjunctival epithelial cells. Indication: For the treatment of ocular itching associated with allergic conjunctivitis.
- Omed - This medication is used to relieve pain and itching from certain ear conditions (e.g., middle ear inflammation with congestion and/or fluid build-up, "swimmer's ear", outer ear inflammation). Benzocaine is a topical anesthetic that helps to numb the pain and itching. Do not use this medication in infants younger than 1 year.
- Omeprazol - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Omeprazol Eco - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Omeprazole - WARNINGS AND PRECAUTIONS Bone Fracture ( 5.3 ) 09/2010 WARNINGS AND PRECAUTIONS Diminished anti-platelet activity of clopidogrel ( 5.4 ) 01/2011 ...
- Omeprazole DR - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Omnipen - Ampicillin is used to treat a wide variety of bacterial infections . It is a penicillin -type antibiotic. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (e.g., common cold , flu ). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.
- Omnitrope - Somatropin belongs to a class of medications known as growth stimulants . Somatropin is a synthetic growth hormone. Growth hormone is made naturally in our bodies by the pituitary gland and is necessary for the stimulation of growth in children. Somatropin is used to treat: growth hormone deficiency in children (to replace growth hormone that they are unable to produce enough of naturally) adults who have growth hormone deficiency (this can result from pituitary disease, surgery...
- Oncovin
- Ondansetron - Warnings and Precautions, ( 5.3 ) 09/2014 1 INDICATIONS AND USAGE ZUPLENZ is a 5-HT3 receptor antagonist indicated for: ...
- Ondansetron Durascan
- Ondansetron ODT
- Ondansetron preservative free
- Ondantor
- Ondaz
- Onzem
- Opehex - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Optimyxin
- Optimyxin Drops
- Optimyxin Plus - Polymyxin b - neomycin compound belongs to the family of medications known as antibacterials . The compound contains a combination of antibiotics used to treat certain types of infections caused by bacteria. The topical ointment can be used to treat some skin infections and to prevent infections in burns, minor cuts, and wounds. The drops are used to treat some types of infections of the eye and ear. The irrigating solution is used to prevent bladder infections in people who have catheters...
- Orbenil
- Orofen - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Orofen Retard - Pharmacological action Ketoprofen is a NSAID, propionic acid derivative. This medication has analgesic, anti-inflammatory and antipyretic activity. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. A pronounced analgesic effect of ketoprofen is due to two mechanisms: peripheral (indirect, via inhibition of...
- Orphenadrine - A muscarinic antagonist used to treat drug-induced parkinsonism and to relieve pain from muscle spasm. [PubChem] Indication: Indicated for the treatment of Parkinson's disease. Orphenadrine is indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions. Orphenadrine is an anticholinergic with a predominantly central effect and only a weak peripheral effect. In addition, it has mild antihistaminic and...
- Orphenadrine; Aspirin; Caffeine ER
- Orstanorm med Heparin
- Osadrox
- Ospamox
- Ospen
- Ospen KV
- Ospen Mega
- Ospexin
- Oxacillin - SPL UNCLASSIFIED SECTION For Intramuscular or Intravenous Injection To reduce the development of drug-resistant bacteria and maintain the effectiveness of Oxacillin for Injection and other antibacterial drugs, Oxacillin for Injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION ...
- Oxaline
- Oxaliplatin - DOSAGE AND ADMINISTRATION ( 2.2 ) 12/2015 WARNINGS AND PRECAUTIONS ( 5.3 , 5.6 , 5.7 ) 12/2015 WARNING: ANAPHYLACTIC REACTIONS Anaphylactic reactions to Oxaliplatin have been reported, and may occur within minutes of Oxaliplatin administration. Epinephrine, corticosteroids, and...
- Oxandrolone - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Oxandrolone Tablets, USP, oral tablets, contain 2.5 mg of the anabolic steroid oxandrolone. Oxandrolone is 17β-hydroxy-17α-methyl-2-oxa-5α-androstan-3-one with the following structural formula: ...
- Oxapax
- Oxaprozin - WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS See full prescribing information for complete boxed warning. ...
- Oxazepam - WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death (see Warnings, Drug Interactions). • Reserve concomitant prescribing of these drugs for use in patients for whom alternative treatment options are inadequate. • Limit dosages...
- Oxipres
- Oxprenolol - A beta-adrenergic antagonist used in the treatment of hypertension, angina pectoris, arrhythmias, and anxiety. [PubChem] Indication: Used in the treatment of hypertension, angina pectoris, arrhythmias, and anxiety. Oxprenolol is a non-selective beta blocker with some intrinsic sympathomimetic activity. Oxprenolol is a lipophilic beta blocker which passes the blood-brain barrier more easily than water soluble beta blockers. As such, it is associated with a higher incidence of CNS-related side...
- Oxybutynine
- PZA-Ciba
- Paclitaxel - SPL UNCLASSIFIED SECTION OAS-OAS/PLV/60/US/PIL-001 237103 Paccal Vet ® -CA1 (paclitaxel for injection) 60 mg paclitaxel per vial Antineoplastic For intravenous use in dogs only Conditionally approved by FDA pending a full demonstration of effectiveness under application number 141-422. ...
- Paizu
- Paluxetil
- Pamafen
- Pamidron - Pamidronate is used to treat high blood calcium levels and certain bone problems (bone metastases/lesions) that may occur with some types of cancer . It is also used to treat a certain type of bone disease (Paget's disease) that causes abnormal and weak bones. Pamidronate belongs to a class of drugs known as bisphosphonates. It works by slowing the release of calcium from bones to lower blood calcium levels, reducing the risk of broken bones ( fractures ) and reducing bone pain.
- Pamidronate - Pamidronic acid (INN) or pamidronate disodium (USAN), marketed as pamidronate disodium pentahydrate under the brand name Aredia, is a bisphosphonate. [Wikipedia] Indication: For the treatment of moderate or severe hypercalcemia associated with malignancy Pamidronate is in a class of drugs called bisphosphonates. Pamidronate reduces breakdown of the bones. Pamidronate is used in the treatment of Paget's disease of bone; to reduce high levels of calcium in the blood associated with malignancy...
- Panam - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Panam Retard - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Pancillin
- Pancuronium - A bis-quaternary steroid that is a competitive nicotinic antagonist. As a neuromuscular blocking agent it is more potent than curare but has less effect on the circulatory system and on histamine release. Indication: Used as a muscle relaxant during anesthesia and surgical procedures. Pancuronium is a typical non-depolarising curare-mimetic muscle relaxant. It acts as a competitive acetylcholine antagonist on neuromuscular junctions, displacing acetylcholine (hence competitive) from its...
- Panthenol - Active ingredients Panthenol (0.5%) Purpose Hair treatment Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Warnings For external use only ...
- Pantoprazole - Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease. Indication: Short-term (up to 16 weeks) treatment of erosive esophagitis. Pantoprazole is a substituted benzimidazole indicated for the short-term treatment (up to 16 weeks) in the healing and symptomatic relief of erosive esophagitis. Pantoprazole is a proton pump inhibitor (PPI) that suppresses the final step in gastric acid...
- Papaverine - An alkaloid found in opium but not closely related to the other opium alkaloids in its structure or pharmacological actions. It is a direct-acting smooth muscle relaxant used in the treatment of impotence and as a vasodilator, especially for cerebral vasodilation. The mechanism of its pharmacological actions is not clear, but it apparently can inhibit phosphodiesterases and it may have direct actions on calcium channels. [PubChem] Indication: For the treatment of impotence and vasospasms....
- Papaverine SR
- Paracetamol - Pharmacological action Paracetamol is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Paracetamol prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in trauma,...
- Paracetamol Comp.
- Paracetamol Conseil - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Paracetamol Sandoz Zapfchen - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Paracetamol; Codeine
- Paricalcitol - 1 INDICATIONS AND USAGE Paricalcitol Injection is an active vitamin D 2 analog indicated for the prevention and treatment of secondary hyperparathyroidism associated with chronic kidney disease (CKD) Stage 5. Paricalcitol Injection is an active vitamin D 2 analog indicated for the prevention and treatment of secondary hyperparathyroidism associated with chronic kidney disease Stage 5. ( 1 ) ...
- Parlodel - This medication is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes (non- insulin -dependent diabetes ). Bromocriptine is an ergot medication that is believed to make your body's insulin function better, improving blood sugar control. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. Proper control of diabetes may also lessen your risk of a heart...
- Paronex
- Paroxetin
- Paroxetine - Pharmacological action Paroxetine is an antidepressant, selective serotonin reuptake inhibitor. This medication has a bicyclic structure distinct from the structures of other known antidepressants. Paroxetine has antidepressant and anxiolytic effects when expressed enough incentive (activated) effect. Antidepressant (thymoleptic) action is related to the ability of paroxetine selectively block the reuptake of serotonin presynaptic membrane than is caused by increase of free content of...
- Passagen
- Pauly
- Pediatric Digoxin
- Peg-Lyte - PEG (polyethylene glycol) with electrolyte is used to clean out the intestines before certain bowel exam procedures such as colonoscopy or barium enema X-rays. It is a laxative that works by drawing large amounts of water into the colon . This effect results in watery bowel movements. Clearing stool from the intestines helps your doctor to better examine the intestines during your procedure. OTHER USES: This section contains uses of this drug that are not listed in the approved US...
- Pen-Vi-K
- Peni G
- Penibrin
- Penibrin Veterinary
- Penicillat
- Penicillin
- Penicillin G Na
- Penicillin G Potassium - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of Penicillin G Potassium and other antibacterial drugs, Penicillin G Potassium for Injection should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Buffered Pfizerpen (penicillin G potassium) for Injection is a...
- Penicillin G Sodium - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of penicillin G sodium and other antibacterial drugs, penicillin G sodium should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Penicillin G sodium for Injection, USP is sterile penicillin G sodium powder for...
- Penicillin-VK
- Penisol
- Penta / 3B
- Penta / 3B + C
- Penta / 3B Plus
- Pentamycetin
- Pentamycetin-HC
- Pentoxifylline - Rx only DESCRIPTION Pentoxil ® (Pentoxifylline Extended-release Tablets, USP) for oral administration contain 400 mg of the active drug and the following inactive ingredients: D&C Red No. 27 Aluminum Lake, FD&C Blue No. 1 Aluminum Lake, hypromellose USP, magnesium stearate NF, polyethylene glycol NF, polysorbate 80 NF, povidone USP, silicon dioxide NF and titanium dioxide USP, in an extended-release formulation. Pentoxifylline is a tri-substituted xanthine derivative...
- Pentoxifylline LP
- Pergolide - SPL UNCLASSIFIED SECTION NADA 141-331, Approved by FDA Dopamine receptor agonist for oral use in horses only SPL UNCLASSIFIED SECTION Caution Federal law restricts this drug to use by or on the order of a licensed veterinarian. Description Prascend Tablets are rectangular light red colored, half-scored...
- Perindopril - Perindopril is a nonsulfhydryl prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is rapidly metabolized in the liver to perindoprilat, its active metabolite, following oral administration. Perindoprilat is a potent, competitive inhibitor of ACE, the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS)....
- Permethrin - SPL UNCLASSIFIED SECTION * w/w Rx Only DESCRIPTION Permethrin Cream, 5% is a topical scabicidal agent for the treatment of infestation with Sarcoptes scabiei (scabies). It is available in an off-white, vanishing cream base. Permethrin Cream, 5% is for topical use only. ...
- Perphenazine - WARNING Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in...
- Perphenazine; Amitriptyline - This medication is used to treat depression occurring with other mental/mood disorders (such as anxiety, agitation, schizophrenia ). This medication is a combination of a tricyclic antidepressant ( amitriptyline ) and an antipsychotic medication ( perphenazine ). Together, they restore the balance of certain natural chemicals in the brain (neurotransmitters such as dopamine, norepinephrine, and serotonin). This medication helps you to have a better mood and sense of well-being, think more...
- Pezeta
- Phendimet SR
- Phendimetrazine - Phendimetrazine is a weight loss medication. Phendimetrazine is chemically related to amphetamines and is a Schedule III drug under the Convention on Psychotropic Substances. In the United States, phendimetrazine is a Schedule III controlled substance under the Uniform Controlled Substances Act of 1970. Indication: Used in the management of exogenous obesity as a short term adjunct (a few weeks) in a regimen of weight reduction based on caloric restriction. Phendimetrazine is a phenylalkylamine...
- Phenobarbital - WARNING: MAY BE HABIT-FORMING DESCRIPTION The barbiturates are nonselective central nervous system (CNS) depressants that are primarily used as sedative-hypnotics. In subhypnotic doses, they are also used as anticonvulsants. The barbiturates and their sodium salts are subject to control under the Federal Controlled Substances Act. Phenobarbital is a...
- Phenol - Active ingredient Phenol 1.4% Purpose Oral Anesthetic/Analgesic Uses temporarily relieves sore throat pain, sore mouth, pain associated with canker sores, minor mouth irritation Warnings Sore throat warning: Severe or persistent sore throat or sore throat...
- Phentermine - A central nervous system stimulant and sympathomimetic with actions and uses similar to those of dextroamphetamine. It has been used most frequently in the treatment of obesity. [PubChem] Indication: For the treatment and management of obesity. Phentermine is indicated in the management of exogenous obesity as a short term (a few weeks) adjunct in a regimen of weight reduction based on caloric restriction. Phentermine hydrochloride is a sympathomimetic amine with pharmacologic activity similar...
- Phentermine YL
- Phentolamine - A nonselective alpha-adrenergic antagonist. It is used in the treatment of hypertension and hypertensive emergencies, pheochromocytoma, vasospasm of raynaud disease and frostbite, clonidine withdrawal syndrome, impotence, and peripheral vascular disease. [PubChem] Indication: Used as an aid for the diagnosis of pheochromocytoma, and may be administered immediately prior to or during pheochromocytomectomy to prevent or control paroxysmal hypertension resulting from anesthesia, stress, or...
- Phenylbutazone - KEEP OUT OF REACH OF CHILDREN FOR HORSES ONLY CAUTION : Federal law restricts this drug to use by or on the order of a licensed veterinarian. DESCRIPTION :...
- Phenylephrine - Phenylephrine is a sympathomimetic amine that acts predominantly on α-adrenergic receptors. It is mainly used to treat nasal congestion, but may also be useful in treating hypotension and shock, hypotension during spinal anaesthesia, prolongation of spinal anaesthesia, paroxysmal supraventricular tachycardia, symptomatic relief of external or internal hemorrhoids, and to increase blood pressure as an aid in the diagnosis of heart murmurs. Indication: Phenylephrine is mainly used to treat...
- Phenyltrope
- Phenytoin - Warnings and Precautions ( 5.11 ) 11/2016 1 INDICATIONS AND USAGE DILANTIN INFATABS are indicated for the treatment of generalized...
- Phlogont Ointment
- Phlogont-Thermal
- Phosphate Sandoz
- Pilocarpine - A slowly hydrolyzed muscarinic agonist with no nicotinic effects. Pilocarpine is used as a miotic and in the treatment of glaucoma. [PubChem] Indication: For the treatment of radiation-induced dry mouth (xerostomia) and symptoms of dry mouth in patients with Sjögrens syndrome. Pilocarpine is a choline ester miotic and a positively charged quaternary ammonium compound. Pilocarpine, in appropriate dosage, can increase secretion by the exocrine glands. The sweat, salivary, lacrimal, gastric,...
- Pindolol - T1999-39 89003701 Visken ® (pindolol) tablets, USP Rx only Visken ® (pindolol), a synthetic beta-adrenergic receptor blocking agent with intrinsic sympathomimetic activity is 1-(Indol-4-yloxy)-3-(isopropylamino)-2-propanol. Its structural formula is: Pindolol is a white to off-white odorless powder soluble in organic solvents and aqueous acids. Visken ® (pindolol)...
- Piperacillin; Tazobactam
- Piracetam
- Piramil - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Pirax
- Piro-Phlogont - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Pirom - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Pirosol - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Piroxicam - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Pixicam - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Platinox
- Plendur
- Plexol - This medication is used as a moisturizer to treat or prevent dry, rough, scaly, itchy skin and minor skin irritations (e.g., diaper rash , skin burns from radiation therapy). Emollients are substances that soften and moisturize the skin and decrease itching and flaking. Some products (e.g., zinc oxide, white petrolatum ) are used mostly to protect the skin against irritation (e.g., from wetness). Dry skin is caused by a loss of water in the upper layer of the skin....
- Polytopic Cream - Polymyxin B sulfate - gramicidin contains a combination of antibiotics used to treat certain types of infections caused by bacteria. The topical cream can be used to treat certain skin infections and to prevent infections in burns, skin grafts, minor cuts, and wounds. The eye/ear drops are used to treat and prevent some types of external infections of the eye and ear. All preparations work by killing the bacteria that cause these infections. Your doctor may have suggested this medication...
- Polytopic Ointment
- Portal
- Potassium
- Potassium Chloride ER
- Pramipexole - Pramipexole is a medication indicated for treating Parkinson’s disease and restless legs syndrome (RLS). It is also sometimes used off-label as a treatment for cluster headache or to counteract the problems with low libido experienced by some users of SSRI antidepressant drugs. Pramipexole has shown robust effects on pilot studies in bipolar disorder. Pramipexole is classified as a non-ergoline dopamine agonist. Indication: For the treatment of signs and symptoms of idiopathic Parkinson's...
- Pravasta Eco
- Pravastatin - Pravastatin is a cholesterol-lowering agent that belongs to a class of medications known as statins. It was derived from microbial transformation of mevastatin, the first statin discovered. It is a ring-opened dihydroxyacid with a 6’-hydroxyl group that does not require in vivo activation. Pravastatin is one of the lower potency statins; however, its increased hydrophilicity is thought to confer advantages such as minimal penetration through lipophilic membranes of peripheral cells,...
- Pravastatina
- Pravastatine
- Pravastatinenatrium
- Prazosin - Prazosin is a selective α-1-adrenergic receptor antagonist used to treat hypertension. It has also been used to decrease urinary obstruction and relieve symptoms associated with symptomatic benign prostatic hyperplasia. α1-Receptors mediate contraction and hypertrophic growth of smooth muscle cells. Antagonism of these receptors leads to smooth muscle relaxation in the peripheral vasculature and prostate gland. Prazosin has also been used in conjunction with cardiac glycosides and...
- Prazosine
- Prednisolon - Pharmacological action Prednisolone is a glucocorticosteroid (GCS). This medication inhibits the function of leukocytes and tissue macrophages. Prednisolone restricts the migration of leukocytes in the area of inflammation. This drug violates the ability of macrophages to phagocytosis and the formation of interleukin-1. Prednisolone contributes to the stabilization of lysosomal membranes, thereby reducing the concentration of proteolytic enzymes in inflammation. This medicine decreases...
- Prednisolone - SPL UNCLASSIFIED SECTION For Oral Use in Dogs Only CAUTION Federal law restricts this drug to use by or on the order of a licensed veterinarian. DESCRIPTION Prednisolone, like methylprednisolone, is a potent anti-inflammatory steroid. Prednisolone, 11,17,21-trihydroxypregna-1,4-diene-3,20-dione, is a synthetic dehydrogenated...
- Prednison
- Prednisone - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Prednisone Tablets USP are available for oral administration containing either 1 mg, 2.5 mg, 5 mg, 10 mg, 20 mg or 50 mg of prednisone USP. Each tablet contains the following inactive ingredients: lactose monohydrate, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium starch glycolate and stearic acid (1 mg, 2.5 mg, and 5 mg only). ...
- Prima-E
- Primum
- Probitor - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Procainamide - A derivative of procaine with less CNS action. [PubChem] Indication: For the treatment of life-threatening ventricular arrhythmias. Procainamide is an agent indicated for production of local or regional anesthesia and in the treatment of ventricular tachycardia occurring during cardiac manipulation, such as surgery or catheterization, or which may occur during acute myocardial infarction, digitalis toxicity, or other cardiac diseases. The mode of action of the antiarrhythmic effect of...
- Prochlorperazine - SPL UNCLASSIFIED SECTION ANTIEMETIC - TRANQUILIZER WARNING SPL UNCLASSIFIED SECTION Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials...
- Profiben
- Profuzosin
- Progesterone - DESCRIPTION Progesterone injection, a progestin, is a sterile solution of progesterone in a suitable vegetable oil available for intramuscular use. Progesterone occurs as a white or creamy white, crystalline powder. It is odorless and is stable in air. Practically insoluble in water, it is soluble in alcohol, acetone, and dioxane and sparingly soluble in vegetable oils. It has the...
- Prohexal
- Prohibit - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Promecilina
- Promethazine - A phenothiazine derivative with histamine H1-blocking, antimuscarinic, and sedative properties. It is used as an antiallergic, in pruritus, for motion sickness and sedation, and also in animals. [PubChem] Indication: For the treatment of allergic disorders, and nausea/vomiting. Promethazine, a phenothiazine, is an H1-antagonist with anticholinergic, sedative, and antiemetic effects and some local anesthetic properties. Promethazine is used as an antiemetic or to prevent motion sickness.
- Propabloc
- Propal - Pharmacological action Propranolol is a non-selective beta-blocker. This medication has antihypertensive, antianginal and antiarrhythmic action. The hypotensive effect is associated with a decrease in minute volume of blood, sympathetic stimulation of peripheral vascular disease, decreased activity of the renin-angiotensin system (has a value in patients with initial hypersecretion of renin), sensitivity of baroreceptors of the aortic arch (not going to enhance their activity in response...
- Propal Retard - Pharmacological action Propranolol is a non-selective beta-blocker. This medication has antihypertensive, antianginal and antiarrhythmic action. The hypotensive effect is associated with a decrease in minute volume of blood, sympathetic stimulation of peripheral vascular disease, decreased activity of the renin-angiotensin system (has a value in patients with initial hypersecretion of renin), sensitivity of baroreceptors of the aortic arch (not going to enhance their activity in response...
- Propantheline - A muscarinic antagonist used as an antispasmodic, in rhinitis, in urinary incontinence, and in the treatment of ulcers. At high doses it has nicotinic effects resulting in neuromuscular blocking. [PubChem] Indication: For the treatment of enuresis. It has also been used for hyperhidrosis, and cramps or spasms of the stomach, intestines or bladder. Propantheline is an anticholinergic drug, a medication that reduces the effect of acetylcholine, a chemical released from nerves that stimulates...
- Propiden
- Propofol-BC
- Propoxyphene - A narcotic analgesic structurally related to methadone. Only the dextro-isomer has an analgesic effect; the levo-isomer appears to exert an antitussive effect. [PubChem] Indication: For the relief of mild to moderate pain Propoxyphene, a synthetic opiate agonist, is structurally similar to methadone. Its general pharmacologic properties are those of the opiates as a group. The analgesic effect of propoxyphene is due to the d-isomer, dextropropoxyphene. It binds to the opiate receptors and leads...
- Propoxyphene Compound 65
- Propoxyphene; Acetaminophen
- Propranolol - Pharmacological action Propranolol is a non-selective beta-blocker. This medication has antihypertensive, antianginal and antiarrhythmic action. The hypotensive effect is associated with a decrease in minute volume of blood, sympathetic stimulation of peripheral vascular disease, decreased activity of the renin-angiotensin system (has a value in patients with initial hypersecretion of renin), sensitivity of baroreceptors of the aortic arch (not going to enhance their activity in response...
- Propranolol; Hydrochlorothiazide
- Prostal
- Prostamustin
- Prostanus
- Prostogenat
- Protamine
- Protogut
- Proventol Expectorant
- Provoltar
- Proxatan
- Proxem - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Pyridostigmine - A cholinesterase inhibitor with a slightly longer duration of action than neostigmine. It is used in the treatment of myasthenia gravis and to reverse the actions of muscle relaxants. [PubChem] Indication: For the treatment of myasthenia gravis. Pyridostigmine is a parasympathomimetic and a reversible cholinesterase inhibitor. Since it is a quaternary amine, it is poorly absorbed in the gut and doesn't cross the blood-brain barrier. Pyridostigmine has a slightly longer duration of action than...
- Quinapril - Quinapril is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is metabolized to quinaprilat (quinapril diacid) following oral administration. Quinaprilat is a competitive inhibitor of ACE, the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS). Quinapril may be used to treat essential hypertension and...
- Quinapril HCT
- Quinidine - An optical isomer of quinine, extracted from the bark of the Cinchona tree and similar plant species. This alkaloid dampens the excitability of cardiac and skeletal muscles by blocking sodium and potassium currents across cellular membranes. It prolongs cellular action potential, and decreases automaticity. Quinidine also blocks muscarinic and alpha-adrenergic neurotransmission. [PubChem] Indication: For the treatment of ventricular pre-excitation and cardiac dysrhythmias Quinidine, a hydantoin...
- Quiril
- Quiril Comp.
- R-Flex
- Radiblock
- Ramipril - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Ramipril HCT
- Ramipril; Hydrochlorthiazid
- Ramixal - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Raniclon
- Ranihexal
- Ranimed
- Ranimed 75 Antacid
- Ranital
- Ranitidin
- Ranitidina
- Ranitidine - Pharmacological action Ranitidine is a blocker of histamine H2-receptors. Inhibits basal and stimulated by histamine, gastrin and acetylcholine (to a lesser extent) the secretion of hydrochloric acid. Increases the pH of gastric contents and reduces the activity of pepsin. The duration of action of ranitidine with a single admission - 12 hours. Pharmacokinetics After oral administration, ranitidine is rapidly absorbed from the gastrointestinal tract. Eating and antacids significantly...
- Ranitidine-BC
- Ranxas
- Regeeva
- Regonol
- Renidone
- Reserpine - An alkaloid found in the roots of Rauwolfia serpentina and R. vomitoria. Reserpine inhibits the uptake of norepinephrine into storage vesicles resulting in depletion of catecholamines and serotonin from central and peripheral axon terminals. It has been used as an antihypertensive and an antipsychotic as well as a research tool, but its adverse effects limit its clinical use. [PubChem] Indication: Foe the treatment of hypertension Reserpine is an adrenergic blocking agent used to treat mild to...
- Reserpine; Hydrochlorothiazide
- Restor
- Retarpen Compositum
- Revitonus C
- Rhinergal
- Rho-Nitro Pumpspray - Nitroglycerin belongs to the class of medications called anti-anginals . Nitroglycerin is used to relieve acute attacks of angina (chest pain). Nitroglycerin relieves acute angina attacks by relaxing blood vessels and increasing the oxygen and blood supply to the heart. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If...
- Rhovane - Pharmacological action Zopiclone is a sleeping drug from group of cyclopyrrolone derivatives. This drug is "non benzodiazepine" agonist of benzodiazepine receptors. Zopiclone also has sedative, anxiolytic, muscle-relaxing center, anticonvulsant and amnesic properties. Like a derivative of benzodiazepine zopiclone enhances GABA-ergic processes in the brain, interacting with the benzodiazepine receptors, as a result of the increased sensitivity of GABA-receptors to the neurotransmitter....
- Rhumalgan SR
- Rhumalgan XL
- Ribavirin - WARNING: RISK OF SERIOUS DISORDERS AND RIBAVIRIN-ASSOCIATED EFFECTS WARNING: RISK OF SERIOUS DISORDERS AND RIBAVIRINASSOCIATED EFFECTS See full prescribing information for complete boxed warning. Ribavirin monotherapy, including...
- Ridazine
- Rifadin
- Rifampicine
- Rifampin - SPL UNCLASSIFIED SECTION Rx Only SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of rifampin for injection, USP and other antibacterial drugs, rifampin should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. ...
- Rifcin
- Rimactan - This medication is a rifamycin antibiotic used to prevent and treat tuberculosis and other infections. This antibiotic treats only bacterial infections . It will not work for viral infections (e.g., common cold , flu ). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.
- Rimactane - This medication is a rifamycin antibiotic used to prevent and treat tuberculosis and other infections. This antibiotic treats only bacterial infections . It will not work for viral infections (e.g., common cold , flu ). Unnecessary use or overuse of any antibiotic can lead to its decreased effectiveness.
- Rimactane Forte
- Rimactazid
- Rimactazid + E
- Rimactazid + Z
- Rimactazid Paed
- Rimactazide
- Rimactazide + Z
- Rimantadine - An RNA synthesis inhibitor that is used as an antiviral agent in the prophylaxis and treatment of influenza. [PubChem] Indication: For the prophylaxis and treatment of illness caused by various strains of influenza A virus in adults. Rimantadine, a cyclic amine, is a synthetic antiviral drug and a derivate of adamantane, like a similar drug amantadine. Rimantadine is inhibitory to the in vitro replication of influenza A virus isolates from each of the three antigenic subtypes (H1N1, H2H2 and...
- Rimcure
- Rimcure 3-FDC
- Rimcure Paed
- Rimmax 2F DC
- Rimstar
- Rimstar 4
- Rimstar 4-FDC
- Rimstar 4FDC
- Rimthree FDC
- Risperidon - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
- Risperidone - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
- Rispolux - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
- Rizatriptan - Rizatriptan is a triptan drug used for the treatment of migraine headaches. It is a selective 5-hydroxytryptamine1 receptor subtype agonist. Indication: For treatment of acute migraine attacks with or without aura. Rizatriptan is a selective agonist of serotonin (5-hydroxytryptamine; 5-HT) type 1B and 1D receptors. It is structurally and pharmacologically related to other selective 5-HT1B/1D receptor agonists and has only a weak affinity for 5-HT1A, 5-HT5A, and 5-HT7 receptors and no...
- Rocap
- Rociject
- Rocillin
- Rocuronium Bromide - 1 INDICATIONS AND USAGE Rocuronium bromide injection is indicated for inpatients and outpatients as an adjunct to general anesthesia to facilitate both rapid sequence and routine tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation. Rocuronium bromide injection is a nondepolarizing neuromuscular blocking agent indicated as an adjunct to general...
- Rolab-Amoclav
- Rolab-Pen-V-K
- Rolazine
- Romin
- Ronal
- Rosiglitazone - Rosiglitazone is an anti-diabetic drug in the thiazolidinedione class of drugs. It is marketed by the pharmaceutical company GlaxoSmithKline as a stand-alone drug (Avandia) and in combination with metformin (Avandamet) or with glimepiride (Avandaryl).Like other thiazolidinediones, the mechanism of action of rosiglitazone is by activation of the intracellular receptor class of the peroxisome proliferator-activated receptors (PPARs), specifically PPARОі. Rosiglitazone is a selective ligand of...
- Rosuvastatin - Rosuvastatin is an antilipemic agent that competitively inhibits hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase. HMG-CoA reducuase catalyzes the conversion of HMG-CoA to mevalonic acid, the rate-limiting step in cholesterol biosynthesis. Rosuvastatin belongs to a class of medications called statins and is used to reduce plasma cholesterol levels and prevent cardiovascular disease. Indication: Used as an adjunct to dietary therapy to treat primary hypercholesterolemia (heterozygous...
- Rotacor
- Rotaqor - Pharmacological action Rotaqor is a lipid-lowering drugs of the statin group. An inhibition of HMG-CoA reductase leads to a series of sequential reactions that result in reduced intracellular cholesterol content and it is a compensatory increase in activity of LDL receptors and thus accelerate the catabolism of LDL cholesterol. The lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. The reduction in LDL cholesterol is dose-dependent and is not...
- Rotet
- Rovit - This medication is a multivitamin product used to treat or prevent vitamin deficiency due to poor diet , certain illnesses, or during pregnancy . Vitamins are important building blocks of the body and help keep you in good health.
- Rovit C - Pharmacological action Ascorbic acid (vitamin c) is essential for the formation of intracellular collagen, is required to strengthen the structure of teeth, bones, and the capillary walls. Vitamin C participates in redox reactions, the metabolism of tyrosine, converting folic acid into folinic acid, metabolism of carbohydrates, the synthesis of lipids and proteins, iron metabolism, processes of cellular respiration. Reduces the need for vitamins B1, B2, A, E, folic acid, pantothenic acid,...
- Roxicam - Pharmacological action Piroxicam is a NSAID, refers to a group oxicams. This medication has anti-inflammatory, analgesic and antipyretic effect. The mechanism of action associated with inhibition of the enzyme COX, which leads to inhibition of prostaglandin synthesis from arachidonic acid. Piroxicam inhibits the aggregation of platelets. For systemic use this medicine reduces the pain syndrome. When Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Roxithromycin - Roxithromycin is a semi-synthetic macrolide antibiotic. It is very similar in composition, chemical structure and mechanism of action to erythromycin, azithromycin, or clarithromycin. Roxithromycin prevents bacteria from growing, by interfering with their protein synthesis. Roxithromycin binds to the subunit 50S of the bacterial ribosome, and thus inhibits the translocation of peptides. Roxithromycin has similar antimicrobial spectrum as erythromycin, but is more effective against certain...
- Roxithromycine
- Roxitromicina
- Roxitromycine
- Rozide
- Rytmogenat
- Sab-Anuzinc HC
- Sab-Anuzinc HC Plus
- Sab-Betaxolol
- Sab-Cortimyxin
- Sab-Dexamethasone
- Sab-Diclofenac
- Sab-Dimenhydrinate
- Sab-Gentamicin
- Sab-Idoxuridine
- Sab-Indomethacin
- Sab-Levobunolol
- Sab-Naproxen - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Sab-Opium and Belladonna
- Sab-Opticort
- Sab-Pentasone
- Sab-Prednase
- Sab-Prednisolone - Pharmacological action Prednisolone is a glucocorticosteroid (GCS). This medication inhibits the function of leukocytes and tissue macrophages. Prednisolone restricts the migration of leukocytes in the area of inflammation. This drug violates the ability of macrophages to phagocytosis and the formation of interleukin-1. Prednisolone contributes to the stabilization of lysosomal membranes, thereby reducing the concentration of proteolytic enzymes in inflammation. This medicine decreases...
- Sab-Prochlorperazine
- Sab-Proctomyxin HC
- Sab-Sodium Chloride - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- Sab-Timolol
- Sab-Tobramycin
- Sab-Trifluridine
- Sabal
- Salbubreathe
- Salbutamol - Salbutamol is a short-acting, selective beta2-adrenergic receptor agonist used in the treatment of asthma and COPD. It is 29 times more selective for beta2 receptors than beta1 receptors giving it higher specificity for pulmonary beta receptors versus beta1-adrenergic receptors located in the heart. Salbutamol is formulated as a racemic mixture of the R- and S-isomers. The R-isomer has 150 times greater affinity for the beta2-receptor than the S-isomer and the S-isomer has been associated with...
- Salinex - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- Salinex Nasal Lubricant
- Sanadorm
- Sanapens
- Sanaxin
- Sandimmune - This medication is used to prevent organ rejection in people who have received a liver , kidney, or heart transplant. It is usually used along with other medications to allow your new organ to function normally. Cyclosporine belongs to a class of drugs known as immunosuppressants. It works by slowing down your body's defense system (immune system) to prevent your body from rejecting a transplanted organ. Because of the risk of severe allergic reactions from intravenous cyclosporine, it should...
- Sandocal D
- Sandocef
- Sandoglobulin - This medication is used to strengthen the body's natural defense system (immune system) to lower the risk of infection in persons with a weakened immune system. This medication is made from healthy human blood that has a high level of certain defensive substances (antibodies), which help fight infections. It is also used to increase the blood count (platelets) in persons with a certain blood disorder (idiopathic thrombocytopenia purpura- ITP ). Platelets are needed to stop bleeding and form...
- Sandomigran - Pizotifen is used to prevent migraine headaches. It is not used to treat headaches once they have started. It is not known exactly how this medication works, but it is thought to affect chemicals, called neurotransmitters, in the brain. This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here. As well, some forms...
- Sandopril
- Sandostatin LAR - Octreotide is a man-made (synthetic) version of a naturally occurring hormone known as somatostatin . Octreotide is used to treat severe diarrhea, flushing, and other symptoms that occur with certain cancers of the intestine. It works by slowing down the release of substances that cause diarrhea and flushing and by increasing water absorption. Octreotide also reduces the amount of growth hormone in the body, and so it is also used to treat acromegaly , a condition associated with...
- Sandostatin LAR Depot - This medication is a long-acting form of octreotide. Octreotide is used to treat severe watery diarrhea and sudden reddening of the face and neck caused by certain types of tumors (e.g., carcinoid tumors , vasoactive intestinal peptide tumors) that are found usually in the intestines and pancreas . The symptoms occur when these tumors make too much of certain natural substances (hormones). This medication works by blocking the production of these hormones. By decreasing watery diarrhea,...
- Sandothal
- Sandovask
- Sandoz Acebutolol - Acebutolol belongs to the class of medications called beta-blockers . It is used to treat high blood pressure and angina (chest pain). It works by reducing the demands put on the heart. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed this with your doctor or are not sure why you are taking this...
- Sandoz Alendronate - Alendronate belongs to a family of medications known as bisphosphonates . It is used to treat and prevent osteoporosis for postmenopausal women. It is also used to treat osteoporosis for men. Alendronate may also be used to treat and prevent steroid-induced osteoporosis for men and women (osteoporosis caused by taking corticosteroids such as prednisone for long periods of time). It may also be used to treat Paget's disease of the bone for both men and women. It works by increasing the...
- Sandoz Alfuzosin - Alfuzosin belongs to a group of medications known as alpha-1 receptor antagonists. It is used to treat the symptoms of enlarged prostate ( benign prostatic hyperplasia or BPH). Alfuzosin helps to relax the muscles in the prostate and the opening of the bladder, which in turn improves urine flow and decreases symptoms of BPH. Alfuzosin does not slow or stop the progression of enlarged prostate. Your doctor may have suggested this medication for conditions other than those listed in these...
- Sandoz Amlodipine - Amlodipine belongs to the family of medications known as calcium channel blockers. Amlodipine is used to treat high blood pressure and angina (chest pain). It works to control blood pressure and reduces the number of angina attacks by widening and relaxing blood vessels.
- Sandoz Anagrelide - Anagrelide belongs to the family of medications called platelet-reducing agents . This medication is used to manage a condition called thrombocythemia, where your body produces too many platelets. Platelets are cells in your blood that help clots to form when you bleed. If your body makes too many platelets, it is hard for your blood to flow normally and it will be more likely to clot or bleed. This can cause medical problems such as heart attacks, stroke, blood clots in the lung or legs...
- Sandoz Anuzinc
- Sandoz Anuzinc HC - This combination product containing two ingredients belongs to a group of medications known as corticosteroids. It is used to treat hemorrhoids. It may also be used to treat discomfort after surgery to the anal area and other conditions affecting the anal area. It works by reducing swelling, irritation, and itching. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be...
- Sandoz Anuzinc HC Plus - This combination product contains 3 medications: pramoxine, hydrocortisone, and zinc sulfate. Pramoxine is a topical anesthetic , which makes the affected areas numb. Hydrocortisone is a corticosteroid with an anti-inflammatory effect. It reduces swelling, itching, and discomfort. Zinc reduces itching and discomfort and helps prevent infection by protecting the areas to which it is applied. This medication is used to relieve pain, swelling, itching, and discomfort in the anal area ...
- Sandoz Anuzinc Plus
- Sandoz Atorvastatin
- Sandoz Azithromycin - Azithromycin belongs to the family of medications known as macrolide antibiotics. It is used to treat certain types of infections that are caused by bacteria. It is most commonly used to treat ear infections (e.g., otitis media), throat infections, lung infections (e.g., pneumonia), and skin infections. It can also be used to prevent mycobacterium avium complex (MAC) infections in people with HIV infection. Your doctor may have suggested this medication for conditions other than the ones...
- Sandoz Betaxolol - Betaxolol belongs to the family of medications known as beta adrenergic blocking agents or "beta-blockers." It is used as an eye drop to lower pressure in the eye to treat chronic open-angle glaucoma or other causes of high pressure inside the eye. The full effects of the eye drops may not be seen for a period of a few weeks. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this...
- Sandoz Brimonidine - Brimonidine belongs to the family of medications known as alpha-2-adrenergic receptor agonists. It is available in eye-drop form and is used to reduce the pressure inside the eye for people with open-angle glaucoma or intraocular hypertension (increased pressure in the eye). Fluid is constantly being formed and drained out of the eye. When this fluid does not drain out of the eye properly, pressure inside the eye increases. Brimonidine works by reducing the amount of fluid produced by...
- Sandoz Bupropion SR - Bupropion belongs to the family of medications known as antidepressants . It is used to treat depression . It works by affecting the balance of chemicals that occur naturally in the brain. For the treatment of depression, the full effects of the medication may not be seen until after several weeks of treatment. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used...
- Sandoz Ca-D
- Sandoz Calcitonin NS
- Sandoz Calcium
- Sandoz Calcium + D
- Sandoz Calcium + Vitamine C
- Sandoz Calcium Injections
- Sandoz Calcium-C
- Sandoz Candesartan
- Sandoz Carbamazepine
- Sandoz Carbamazepine CR
- Sandoz Cefprozil - Cefprozil is an antibiotic that belongs to the family of medications known as cephalosporins . It is used to treat certain types of infections caused by bacteria. It is most commonly used to treat infections of the throat, ear, sinus, skin, and bladder. It works by weakening the cell walls of the bacteria causing the infection, thereby killing the bacteria. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well,...
- Sandoz Clarithromycin - Clarithromycin belongs to the group of medications called macrolide antibiotics. It is used to treat infections caused by certain bacteria. It works by killing or stopping the growth of bacteria that can cause certain infections. Clarithromycin may be prescribed for people with bacterial throat infections, sinus infections, ear infections, bronchitis, pneumonia, and skin infections such as impetigo and cellulitis. Clarithromycin may also be used to prevent and treat certain...
- Sandoz Clonazepam - Pharmacological action Clonazepam is an antiepileptic drugs from the group of benzodiazepine derivatives. This medication has a pronounced anticonvulsant and central muscle relaxant, anxiolytic, sedative and hypnotic effects. Clonazepam strengthens the inhibitory effect of GABA on the transmission of nerve impulses. Anxiolytic effects of this drug is due to the influence on the amygdaloid complex of the limbic system and appears in reducing the emotional stress, reduce anxiety, fear,...
- Sandoz Cortimyxin
- Sandoz Cyclosporine - Cyclosporine belongs to the groups of medications known as immunosuppressant agents. It is used to prevent the rejection of organ transplants and bone marrow transplants by suppressing the body's natural defence, the immune system. It is also used to treat rheumatoid arthritis, which is thought to be caused by the body's own immune system attacking the joints of the body. Cyclosporine is also used to treat severe psoriasis when other treatments have not been effective. It has also been...
- Sandoz Dexamethasone - Dexamethasone belongs to the family of medications known as corticosteroids . Dexamethasone eye drops and ointment are used to treat a number of eye conditions associated with inflammation of the eye (e.g., allergic conjunctivitis). Dexamethasone works by reducing inflammation, irritation, and redness. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of...
- Sandoz Diclofenac
- Sandoz Diclofenac Rapide
- Sandoz Diclofenac SR
- Sandoz Diltiazem CD - Diltiazem belongs to a family of medications known as calcium channel blockers . It is used to treat high blood pressure and angina (chest pain). It works by relaxing blood vessels and by reducing the workload of the heart. The injectable form of this medication is sometimes used in the hospital to bring abnormal heart rhythms under control. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of...
- Sandoz Diltiazem T - Diltiazem belongs to a family of medications known as calcium channel blockers . It is used to treat high blood pressure and angina (chest pain). It works by relaxing blood vessels and by reducing the workload of the heart. The injectable form of this medication is sometimes used in the hospital to bring abnormal heart rhythms under control. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of...
- Sandoz Dimenhydrinate
- Sandoz Dorzolamide
- Sandoz Dorzolamide; Timolol
- Sandoz Enalapril
- Sandoz Eyelube
- Sandoz Famciclovir - Famciclovir belongs to the family of medications known as antivirals . It is used to treat genital herpes and prevent recurring episodes of genital herpes. It is also used to treat shingles (a painful rash caused by some herpes viruses, also known as herpes zoster). These infections are caused by viruses. Famciclovir prevents the virus from making DNA (genetic material) and copying itself, and so leads to lower levels of virus in the blood. It helps to prevent the virus from...
- Sandoz Felodipine - Felodipine belongs to a class of medications called calcium channel blockers . It is used to treat high blood pressure . It controls blood pressure by relaxing blood vessels and reducing the workload of the heart. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed this with your doctor or are not...
- Sandoz Fenofibrate S - Fenofibrate belongs to the class of medications known as fibrates . It is used in addition to diet and exercise to treat people with certain types of abnormal cholesterol levels. Fenofibrate reduces bad cholesterol (low density lipoproteins [LDL] and very low density lipoproteins [VLDL]) and triglycerides in your blood. It also increases good cholesterol (high density lipoprotein [HDL]) levels. Bringing cholesterol levels in the blood into the desired range has been shown to reduce the...
- Sandoz Fentanyl - Fentanyl belongs to a group of medications called opioids. Fentanyl is used to treat persistent chronic (long-term) moderate-to-severe pain for those who need constant pain relief and are currently taking other opioid (narcotic) medications. It acts on the brain to increase pain tolerance. This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or approved for all...
- Sandoz Finasteride
- Sandoz Finasteride A - Finasteride belongs to a group of medications known as 5 alpha-reductase inhibitors . It is used to treat male pattern baldness by preventing the enzyme 5 alpha-reductase from converting testosterone to its active form in the body (dihydrotestosterone or DHT). DHT plays a major role in inherited male pattern baldness (androgenic alopecia), and by preventing its production finasteride can stimulate hair growth in many men with mild to moderate inherited male pattern baldness. The...
- Sandoz Fluoxetine - Fluoxetine belongs to a class of medications called selective serotonin reuptake inhibitors (SSRIs). It is used for the treatment of depression and helps to elevate mood. Selective serotonin reuptake inhibitors work by increasing the amount of a neurotransmitter, called serotonin, that is available in certain parts of the brain. Although you may start feeling better within a few weeks of treatment, the full effects of the medication may not be evident until several weeks of treatment have...
- Sandoz Fluvoxamine - Fluvoxamine belongs to the class of medications called selective serotonin reuptake inhibitors (SSRIs). It is used to treat depression and obsessive-compulsive disorder (OCD). It helps to reduce anxiety and unpleasant thoughts associated with OCD and improves mood by treating depression. Serotonin reuptake inhibitors are thought to work by increasing the amount of a neurotransmitter (a chemical found in the brain) called serotonin . Although you may start feeling better within a few...
- Sandoz Gentamicin - Gentamicin belongs to the family of medications known as antibiotics . It is used to treat infections of the eye or ear that are caused by certain bacteria. It works by blocking the metabolism of the bacteria and this then kills the bacteria. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed this...
- Sandoz Gliclazide
- Sandoz Glyburide - Glyburide is an antidiabetes medication that belongs to the family of medications known as sulfonylureas . It is used to treat high blood sugar (hyperglycemia) in people with type 2 diabetes. Antidiabetes medications such as glyburide are used when diet, exercise, and weight reduction have not been found to lower blood sugar well enough on their own. Glyburide increases the release of insulin (a hormone produced by the pancreas that allows sugar to enter into cells where it is needed for...
- Sandoz Idoxuridine
- Sandoz Indomethacin - Indomethacin belongs to the class of medications known as nonsteroidal anti-inflammatories (NSAIDs). It works by reducing pain, swelling, and inflammation. Indomethacin is used for the relief of mild to moderately severe pain accompanied by inflammation. It can be used for people with conditions such as rheumatoid arthritis, osteoarthritis, ankylosing spondylitis, and gout. Your doctor may have suggested this medication for conditions other than the ones listed in these drug information...
- Sandoz Irbesartan - Irbesartan information Irbesartan is a drug that classified as an Angiotensin II receptor antagonist. Irbesartan indications This blood pressure medication (Irbesartan Zydus Pharmaceuticals) is indicated for the treatment of hypertension or high blood pressure. Irbesartan works by preventing the narrowing of blood vessels and arteries and it also prevents the constriction of the flow of blood. Buy Irbesartan Zydus Pharmaceuticals, as it is also prescribed for the treatment of kidney...
- Sandoz Irbesartan HCT
- Sandoz K
- Sandoz Leflunomide - Leflunomide information This medication, with the generic name of Leflunomide, is specially formulated to provide physical relief from inflammation, swelling, stiffness, and joint pain as caused by rheumatoid arthritis. Leflunomide acts by stopping the production of too much immune cells causing inflammation and swelling in the body. Leflunomide indications Leflunomide is prescribed to patients showing signs of rheumatism as listed below: Inflammation Swelling Stiffness Joint pain ...
- Sandoz Letrozole - Letrozole belongs to the group of cancer-fighting medications known as antineoplastics , and specifically to the type of antineoplastics known as nonsteroidal aromatase inhibitors . Letrozole can be used to treat advanced breast cancer in postmenopausal women , including those who are no longer getting the beneficial effects of antiestrogen medications such as tamoxifen. Letrozole can also reduce the risk of breast cancer recurrence in postmenopausal women who have been successfully...
- Sandoz Levobunolol
- Sandoz Levofloxacin - Levofloxacin belongs to the class of medications called quinolones . It is an antibiotic used for the treatment of certain bacterial infections. It is most commonly used to treat infections of the bladder, kidney, prostate, sinus, skin, and lung. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed...
- Sandoz Lisinopril
- Sandoz Lisinopril HCT
- Sandoz Memantine - Memantine belongs to the group of medications known as NMDA receptor antagonists . It is used alone or with other medications to treat people with moderate-to-severe Alzheimer's disease. Memantine does not cure Alzheimer's disease, but it is used to decrease the symptoms. It works in the brain to block the effect of some chemicals that cause symptoms of Alzheimer's disease such as decreased memory and other mental functions. Your doctor may have suggested this medication for conditions...
- Sandoz Metformin FC - Metformin belongs to the class of medications called oral hypoglycemics, which are medications that lower blood sugar. It is used to control blood glucose (blood sugar) for people with type 2 diabetes. It is used when diet, exercise, and weight reduction have not been found to lower blood glucose well enough on their own. Metformin works by reducing the amount of glucose made by the liver and by making it easier for glucose to enter into the tissues of the body. Metformin has been found...
- Sandoz Methylphenidate SR - Methylphenidate belongs to the family of medications known as stimulants . It is used to treat attention deficit hyperactivity disorder (ADHD) and narcolepsy (uncontrollable need to sleep). It helps to increase attention and decrease restlessness in children and adults who have been diagnosed with ADHD. Other measures (e.g., psychological, educational, and social therapies) are used along with methylphenidate as part of an overall treatment program for ADHD. This medication also helps to...
- Sandoz Metoprolol SR - Metoprolol belongs to the class of medications called beta-blockers. Metoprolol is used to treat high blood pressure and prevent the symptoms of angina (chest pain). It is also used to help reduce the risk of death right after a heart attack. It works by reducing the demands put on the heart. Metoprolol is also taken by people who have had a heart attack to reduce the risk of having another one. Metoprolol is often used in combination with other high blood pressure medications such as...
- Sandoz Metoprolol Type L
- Sandoz Morphine SR
- Sandoz Nabumetone
- Sandoz Naratriptan
- Sandoz Nitrazepam - Nitrazepam belongs to the class of medications called benzodiazepines. It is used for short-term treatment of sleeping problems (insomnia), such as difficulty falling asleep, frequent awakenings during the night, and early-morning awakening. It is also used to manage myoclonic seizures. It works by slowing down the nerves in the brain (the central nervous system). Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. ...
- Sandoz Olanzapine - Olanzapine belongs to group of medications known as antipsychotic/antimanic agents. Olanzapine is used to treat schizophrenia and related mental disorders, as well as bipolar disorder. Schizophrenia can cause symptoms such as hallucinations (e.g., hearing, seeing, or sensing things that are not there), delusions, unusual suspiciousness, and emotional withdrawal. People with this condition may also feel depressed, anxious, or tense. Bipolar disorder causes alternating periods of...
- Sandoz Olanzapine ODT - Olanzapine belongs to group of medications known as antipsychotic/antimanic agents. Olanzapine is used to treat schizophrenia and related mental disorders, as well as bipolar disorder. Schizophrenia can cause symptoms such as hallucinations (e.g., hearing, seeing, or sensing things that are not there), delusions, unusual suspiciousness, and emotional withdrawal. People with this condition may also feel depressed, anxious, or tense. Bipolar disorder causes alternating periods of...
- Sandoz Omeprazole - Omeprazole belongs to the family of medications called proton pump inhibitors (PPIs). It slows or prevents the production of acid within the stomach. It is used to treat conditions where reduction in acid secretion is required for proper healing, including stomach and intestinal ulcers (gastric and duodenal ulcers), the prevention and treatment of ulcers associated with medications known as NSAIDs, reflux esophagitis, Zollinger-Ellison syndrome, heartburn, and gastroesophageal reflux...
- Sandoz Ondansetron - Ondansetron belongs to the class of medications called 5-HT3 receptor antagonists. This medication is used to prevent nausea and vomiting associated with certain types of cancer chemotherapy and radiation. It is also used to prevent and treat the nausea and vomiting that occurs after surgery. It works by reducing the effects of a naturally-occurring chemical in the body called serotonin, which causes nausea and vomiting. This medication may be available under multiple brand names...
- Sandoz Opium and Belladonna
- Sandoz Opticort
- Sandoz Orphenadrine - Orphenadrine belongs to the group of medications called s keletal muscle relaxants . It is used to treat acute muscle spasms. Muscle tightening or spasms result largely from signals in the nervous system telling the muscles to tighten or contract. Orphenadrine helps to relieve muscle tightening and stiffness by reducing the strength of those signals in the nervous system. Muscle relaxants such as orphenadrine are used to help relieve the stiffness, pain, and discomfort caused by sprains...
- Sandoz Oxycodone; Acetaminophen
- Sandoz Pantoprazole - Pantoprazole belongs to the family of medications called proton pump inhibitors (PPIs). Proton pump inhibitors are used to treat conditions such as stomach ulcers, intestinal ulcers, and gastroesophageal reflux disease (GERD, reflux esophagitis) by reducing the amount of acid the stomach produces. Pantoprazole is also sometimes used along with antibiotics to treat stomach ulcers that are caused by bacteria known as H. pylori. Pantoprazole can also be used to treat or reduce the risk of...
- Sandoz Paroxetine - Paroxetine belongs to the class of medications called selective serotonin reuptake inhibitors (SSRIs). It is used to treat depression, obsessive-compulsive disorder, panic disorder, social phobia (social anxiety disorder), generalized anxiety disorder, and posttraumatic stress disorder. It works by affecting the balance of chemicals in the brain that are associated with depression and anxiety disorders. It may take several weeks before the full beneficial effects of this medication are...
- Sandoz Pentasone - Betamethasone sodium phosphate - gentamicin eye-ear drops contain an antibiotic (gentamicin) and a corticosteroid (betamethasone). The antibiotic helps to clear up infections of the eye or ear caused by bacteria. The corticosteroid helps to reduce swelling, inflammation, and irritation of the affected area. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used...
- Sandoz Pindolol
- Sandoz Pioglitazone - Pioglitazone is a member of the family of medications known as thiazolidinediones . It is used to lower high blood sugar associated with type 2 diabetes. Thiazolidinediones such as pioglitazone help insulin to work more effectively. By keeping blood sugar at a desired level, pioglitazone can help to prevent or delay the long-term problems associated with uncontrolled high blood sugar (e.g., kidney disease, eye problems, nerve problems, heart disease). Pioglitazone may be used alone when...
- Sandoz Pramipexole - Pramipexole belongs to the class of medications called dopamine agonists. It is used to treat signs and symptoms of Parkinson's disease. It is also used to treat symptoms of moderate to severe restless leg syndrome. It helps to improve muscle control and movement by affecting the balance of a chemical in the brain called dopamine.
- Sandoz Prednisolone
- Sandoz Prochlorperazine - Prochlorperazine belongs to the group of medications known as antipsychotics , and specifically to the family of antipsychotics called phenothiazines . It is used to treat the symptoms of psychotic disorders such as excessive anxiety, tension, confusion, delusions, and agitation. It works by affecting the chemical balance in the brain. It also can be used to treat or prevent nausea and vomiting caused by the use of certain medications (e.g., cancer treatments) or motion sickness....
- Sandoz Proctomyxin HC - This medication is a combination product that is used for the reduction of swelling, pain, and inflammation of hemorrhoids and other rectal lesions. It is also used to treat proctitis, fissures, cryptitis, pain following rectal surgery, and rectal itching. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not...
- Sandoz Quetiapine - Quetiapine belongs to a class of medications known as antipsychotics. It is used to treat symptoms of schizophrenia, manic episodes associated with bipolar disorder, and depressive episodes associated with bipolar disorder. It works by affecting the actions of certain chemicals in the brain known as neurotransmitters. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not...
- Sandoz Rabeprazole - Rabeprazole belongs to the class of medications known as proton pump inhibitors (PPIs). It works by slowing or preventing the production of acid in the stomach. Rabeprazole is used to treat and maintain healing of gastroesophageal reflux disease (GERD). It is also used to treat symptoms, such as heartburn and regurgitation, of non-erosive reflux disease (NERD). It is also used for short-term treatment in the healing and relief of symptoms associated with duodenal and gastric ulcers....
- Sandoz Ramipril - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Sandoz Ranitidine - Ranitidine belongs to the class of medications called H2-antagonists . Ranitidine is used to reduce the amount of acid secreted by the stomach in order to reduce ulcer and heartburn pain or to assist in healing of ulcers. It is used to treat stomach and duodenal (intestinal) ulcers, and gastroesophageal reflux disease (GERD). Ranitidine is also used to prevent ulcers in certain circumstances and to treat a condition associated with large amounts of stomach acid secretion known as...
- Sandoz Repaglinide
- Sandoz Risedronate - Risedronate belongs to a group of medications called bisphosphonates. It is used to treat and prevent osteoporosis for women who are past menopause and to treat and prevent osteoporosis caused by treatment with corticosteroids (e.g., prednisone) for men and women. It is also used to improve bone mineral density for men with osteoporosis, and to treat a condition called Paget's disease. Risedronate increases the thickness of bone ( bone mineral density ) by slowing down the cells that...
- Sandoz Risperidone - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
- Sandoz Rivastigmine - Rivastigmine belongs to a family of medications known as cholinesterase inhibitors . It is used to treat symptoms of mild to moderate Alzheimer's disease. It is also used to treat mild to moderate dementia (problems with brain functions such as memory, language, and thinking) associated with Parkinson's disease. Alzheimer's disease is caused by the constant degeneration of certain nerve cells in the brain that make a chemical called acetylcholine . This chemical is thought to be important...
- Sandoz Salbutamol
- Sandoz Schmerzgel
- Sandoz Sodium Bicarbonate
- Sandoz Sodium Chloride - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- Sandoz Sumatriptan
- Sandoz Tamsulosin
- Sandoz Tamsulosin CR - Tamsulosin belongs to a group of medications known as alpha 1A receptor antagonists . It is used to treat symptoms of enlarged prostate ( benign prostatic hyperplasia [BPH]). As the prostate gland enlarges, it can put pressure on the urethra , the tube that carries urine away from the bladder to be expelled. This causes a weak urine stream or a feeling of not being able to empty the bladder completely. Tamsulosin helps to relax the muscles in the prostate and the opening of the bladder....
- Sandoz Timolol - This medication belongs to the family of medications called beta-blockers. Timolol eye drops are used to treat glaucoma and increased pressure in the eye. This medication works by reducing the production of fluid in the eye, thereby lowering the pressure in the eye. It may take up to 4 weeks for the eye drops to lower the pressure in the eye to a satisfactory level. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. ...
- Sandoz Tobramycin - Tobramycin belongs to the class of medications called antibiotics. It is used to treat certain eye infections that are caused by bacteria. It works by helping to kill the bacteria that are causing the infection. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed this with your doctor or are not...
- Sandoz Trifluridine - Trifluridine belongs to a group of medications known as antivirals. It is used to treat certain eye infections caused by herpes simplex virus types 1 and 2. It works by killing the virus that causes the infection.
- Sandoz Valproic - Valproic acid belongs to the class of medications called anticonvulsants . It is used to manage and control of certain types of seizures. It works on the central nervous system (CNS) in the brain to reduce the number and severity of seizures. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions discussed here. If you have not discussed...
- Sandoz Valsartan
- Sandoz Valsartan HCT - This is a combination product that contains 2 medications: valsartan and hydrochlorothiazide. This combination medication is used to treat high blood pressure . Valsartan belongs to the class of medications called angiotensin II receptor blockers and helps to lower blood pressure by relaxing blood vessels. Hydrochlorothiazide belongs to the class of medications called diuretics or "water pills" and helps control blood pressure by getting rid of excess salt and water. The full...
- Sandoz Venlafaxine XR - Venlafaxine belongs to the class of antidepressant and anxiolytic medications known as serotonin and norepinephrine reuptake inhibitors (SNRIs). It is used to treat depression. It works on the central nervous system (CNS) to elevate mood in people with depression. Venlafaxine is also used to treat the symptoms of anxiety causing distress in generalized anxiety disorder (GAD), social anxiety disorder (social phobia), and panic disorder (panic attacks). SNRIs work by increasing the amount...
- Sandoz Zolmitriptan
- Sandoz Zolmitriptan ODT
- Sandoz Zopiclone - Pharmacological action Zopiclone is a sleeping drug from group of cyclopyrrolone derivatives. This drug is "non benzodiazepine" agonist of benzodiazepine receptors. Zopiclone also has sedative, anxiolytic, muscle-relaxing center, anticonvulsant and amnesic properties. Like a derivative of benzodiazepine zopiclone enhances GABA-ergic processes in the brain, interacting with the benzodiazepine receptors, as a result of the increased sensitivity of GABA-receptors to the neurotransmitter....
- Sangofer
- Sanorex
- Sansert
- Santis
- Sanval
- Sartaxal
- Scabanca
- Sclerace - Ramipril information Ramipril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Ramipril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Ramipril is also used for the prevention of heart attacks, stroke and other heart related problems. Ramipril warnings The medication is major allergen especially to patients...
- Secef
- Secubar - Lisinopril information Lisinopril is a popular drug that belongs to a wide class of medicines generally known as ACE inhibitors (angiotensin converting enzyme inhibitors). This product is generally prescribed to patients who are suffering from congestive heart failure, high blood pressure or to patients who have recently suffered a heart attack. Lisinopril indications This medication is a well known medicine that is generally prescribed to patients who are suffering from heart medical...
- Secubar Diu
- Sedacoron
- Sedasol Eco Natura
- Sedasol Econatura
- Selegiline - Pharmacological action Selegiline is an almost near-to-white crystalline powder that is round, convex, scored, and uncoated tablet. Selegiline is freely soluble in water. Selegiline is used to treat Parkinson's disease, a disease associated with low levels of dopamine in your brain. The question how really Selegiline works is not known but it is believed to prevent the breakdown of dopamine in your brain. After levedopa or carbidopa therapy begins to deteriorate, selegiline is usually...
- Senna - Active ingredient (in each tablet) Sennosides 8.6mg Ask a doctor or pharmacist before use if you are taking any other drug. Take this product tow or more hours before or after other drugs. Laxatives may affect how other drugs work. Ask a doctor before use if you have noticed a sudden change in bowel habits that lasts over two weeks. ...
- Serodur
- Serolux
- Seronil
- Sertiva
- Sertralin
- Sertralin Eco
- Sertralina
- Sertraline - Pharmacological action Sertraline (with the generic name of Sertraline) belongs to the groups of drugs known as selective serotonin reuptake inhibitors. These selective serotonin reuptake drugs influence chemical imbalance in the brain responsible for depression, panic anxiety, obsessive compulsive disorder and others. Why is Sertraline prescribed? Sertraline is indicated for the treatment of: depression panic anxiety disorders obsessive compulsive disorder PSTD or post traumatic...
- Sertrin
- Servamox
- Servamox CLV
- Servamox CLV 12H
- Servamox-F
- Servicef
- Serviclazide
- Serviclor
- Servicol
- Servidoxyne
- Serviflox
- Servigenta
- Servigesic - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Servimeta
- Servimox - Pharmacological action Amoxicillin is an antibiotic of group semisynthetic penicillins a wide spectrum of action. It is a 4-hydroxyl analog of ampicillin. It has bactericidal action. amoxicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (except strains producing penicillinase), Streptococcus spp; aerobic gram-negative bacteria: Neisseria Gonorrhoeae, Neisseria Meningitidis, Escherichia Coli, Shigella spp., Salmonella spp., Klebsiella spp. Microorganisms...
- Servinaprox
- Servipep
- Serviradine
- Servispor
- Servitrim
- Servitrim Forte
- Servitrim-F
- Servitrocin - Pharmacological action Erythromycin is a macrolide antibiotic. Has bacteriostatic action. However at higher doses against susceptible organisms has a bactericidal effect. erythromycin is reversibly bound to the ribosome of bacteria, thereby inhibiting protein synthesis. Erythromycin is active against gram-positive bacteria: Staphylococcus spp. (strains producing and not producing penicillinase), Streptococcus spp. (including Streptococcus pneumoniae); gram-negative bacteria: Neisseria...
- Servizol
- Sevambutol
- Sicorten Plus
- Simcora - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simplaqor - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simva - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simvahex - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simvahexal - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simvastatin - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simvastatina - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simvastatine - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Simvastatine Biostabilex - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Sinepress
- Sodium Aurothiomalate
- Sodium Bicarbonate - Enter section text here Active ingredient Purpose (in each tablet) Sodium bicarbonate 10 gr (650 mg) ....... Antacid Enter section text...
- Sodium Chloride - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- Sodium Phosphates - Your doctor may prescribe this product (usually along with other products) to clean stool from the intestines before surgery or certain bowel procedures (such as colonoscopy , radiography). Use it only as directed by your doctor. It may also be used to relieve occasional constipation . However, when treating constipation, you should use milder products (such as stool softeners, bulk-forming laxatives) whenever possible. Talk to your doctor or pharmacist about other treatment options. Sodium...
- Sodium Sulamyd - This is a sulphonamide antibiotic used to treat conjunctivitis (inflammation in the eye caused by bacteria), corneal ulcer, and other superficial eye infections . It works by preventing the bacteria that cause the infection and irritation from growing and reproducing. This causes the infection to clear. This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or...
- Sodium Sulamyd with Methylcellulose
- Solumag
- Solutrat
- Somnipar
- Sonazine
- Sonsuur
- Sotahexal
- Sotalol - An adrenergic beta-antagonist that is used in the treatment of life-threatening arrhythmias. [PubChem] Indication: For the maintenance of normal sinus rhythm [delay in time to recurrence of atrial fibrillation/atrial flutter (AFIB/AFL)] in patients with symptomatic AFIB/AFL who are currently in sinus rhythm. Also for the treatment of documented life-threatening ventricular arrhythmias. Sotalol is an antiarrhythmic drug. It falls into the class of beta blockers (and class II antiarrhythmic...
- Sotaryt
- Spacin
- Sparkal
- Sparkal Mite
- Sparzid
- Spasmenzyme
- Spasmoflex
- Spaxim
- Spectroxyl
- Spiramycine; Metronidazole
- Spironolacton - Pharmacological action Spironolactone is a potassium, magnesium sparing diuretic. This medication is a competitive antagonist of aldosterone on the effect on distal nephron (competes for binding sites on cytoplasmic protein receptors, reduces the synthesis of permeases in the aldosterone-sensitive part of collecting tubules and distal tubules), increases the excretion of Na+, Cl- and water and reduces the excretion of K+ and urea, reduces the titratable acidity of urine. Increased diuresis...
- Spironolactone - SPL UNCLASSIFIED SECTION Rx only WARNING Spironolactone has been shown to be a tumorigen in chronic toxicity studies in rats (see Precautions ). Spironolactone should be used only in those conditions described under Indications and Usage ...
- Spironolactone; Hydrochlorothiazide
- Standacillin
- Star-Pen
- Stomacer
- Sucralfaat
- Sufentanil - An opioid analgesic that is used as an adjunct in anesthesia, in balanced anesthesia, and as a primary anesthetic agent. [PubChem] Indication: Used as an analgesic adjunct in anesthesia and as a primary anesthetic drug in procedures requiring assisted ventilation and in the relief of pain. Sufentanil is a synthetic opioid analgesic. Sufentanil interacts predominately with the opioid mu-receptor. These mu-binding sites are discretely distributed in the human brain, spinal cord, and other tissues...
- Suifac - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
- Suiflox
- Suipen
- Sulcef
- Sulfadiazine - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Sulfadiazine is an oral sulfonamide anti-bacterial agent. Each tablet, for oral administration, contains 500 mg sulfadiazine. In addition, each tablet contains the following inactive ingredients: croscarmellose sodium, docusate sodium, microcrystalline cellulose, povidone, sodium benzoate,...
- Sulfamethoxazole - A bacteriostatic antibacterial agent that interferes with folic acid synthesis in susceptible bacteria. Its broad spectrum of activity has been limited by the development of resistance. (From Martindale, The Extra Pharmacopoeia, 30th ed, p208) Indication: For the treatment bacterial infections causing bronchitis, prostatitis and urinary tract infections. Sulfamethoxazole is a sulfonamide drug that inhibits bacterial synthesis of dihydrofolic acid by competing with para-aminobenzoic acid (PABA)...
- Sulfamethoxazole; Trimethoprim
- Sulfisoxazole - A short-acting sulfonamide antibacterial with activity against a wide range of gram- negative and gram-positive organisms. [PubChem] Indication: For the treatment of severe, repeated, or long-lasting urinary tract infections, meningococcal meningitis, acute otitis media, trachoma, inclusion conjunctivitis, nocardiosis, chancroid, toxoplasmosis, malaria and other bacterial infections. Sulfisoxazole is a sulfonamide antibiotic. The sulfonamides are synthetic bacteriostatic antibiotics with a wide...
- Sulindac - Cardiovascular Risk NSAIDs may cause an increased risk of serious cardiovascular thrombotic events, myocardial infarction, and stroke, which can be fatal. This risk may increase with duration of use. Patients with cardiovascular disease or risk factors for cardiovascular disease may be at greater risk. (See WARNINGS ...
- Sulpiride - A dopamine D2-receptor antagonist. It has been used therapeutically as an antidepressant, antipsychotic, and as a digestive aid. (From Merck Index, 11th ed) Indication: Sulpiride is indicated for the treatment of schizophrenia. Sulpiride is a substituted benzamide derivative and a selective dopamine D2 antagonist with antipsychotic and antidepressant activity. Other benzamide derivatives include metoclopramide, tiapride, and sultopride.
- Sumatran
- Sumatriptan - Pharmacological action Sumatriptan is a drug in tablet pharmaceutical form that has sumatriptan as the active element. This drug under trade name Imitrex also contains inactive elements such as the following: croscarmellose sodium; dibasic calcium phosphate; magnesium stearate; microcrystalline cellulose; sodium bicarbonate; hypromellose; iron oxide; titanium dioxide; traction Sumatriptan is a drug used to alleviate the headache brought about by migraine attacks. Why is Sumatriptan...
- Supeudol - Oxycodone belongs to a group of medications known as opioid analgesics (narcotic pain relievers). It is used to relieve moderate to severe pain. It decreases pain by working on the central nervous system.
- Supplin - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
- Surpas
- Syeda - This medication is a combination of 2 hormones: an estrogen (ethinyl estradiol ) and a progestin (drospirenone). This product is used to prevent pregnancy . It works mainly by preventing the release of an egg ( ovulation ) during your menstrual cycle. It also makes vaginal fluid thicker to help prevent sperm from reaching an egg (fertilization) and changes the lining of the uterus (womb) to prevent attachment of a fertilized egg. If a fertilized egg does not attach to the uterus, it...
- Syntocinon
- Tacrolimus - Warnings and Precautions, Use with CYP3A4 Inhibitors and Inducers ( 5.13 ) 08/2013 Warnings and Precautions, QT Prolongation ( 5.14 ) 08/2013 Warnings and Precautions, Gastrointestinal Perforation ( 5.18 ) 08/2013 BOX WARNING - MALIGNANCIES AND SERIOUS INFECTIONS ...
- Tafen
- Tafen Nasal
- Tafen Novolizer
- Talnur
- Tamec
- Tamoxifen - One of the selective estrogen receptor modulators with tissue-specific activities. Tamoxifen acts as an anti-estrogen (inhibiting agent) in the mammary tissue, but as an estrogen (stimulating agent) in cholesterol metabolism, bone density, and cell proliferation in the endometrium. [PubChem] Indication: For the treatment of breast cancer. Tamoxifen belongs to a class of drugs called selective estrogen receptor modulators (SERMs), which have both estrogenic and antiestrogenic effects. Tamoxifen...
- Tamoxifene - Tamoxifen belongs to the group of cancer-fighting medications known as antineoplastics , and specifically to the type of antineoplastics known as antiestrogens . It is used in combination with other medications to treat early breast cancer . Tamoxifen fights certain types of breast cancer, called hormone response or estrogen positive breast cancer, by blocking the effects of the hormone estrogen in the body. This prevents the growth of the types of breast cancer cells that require...
- Tamoxigenat
- Tamsulosin - Tamsulosin is a selective antagonist at alpha-1A and alpha-1B-adrenoceptors in the prostate, prostatic capsule, prostatic urethra, and bladder neck. At least three discrete alpha1-adrenoceptor subtypes have been identified: alpha-1A, alpha-1B and alpha-1D; their distribution differs between human organs and tissue. Approximately 70% of the alpha1-receptors in human prostate are of the alpha-1A subtype. Blockage of these receptors causes relaxation of smooth muscles in the bladder neck and...
- Tamsulosine
- Tamsulosine LP
- Tamsulosine Retard
- Tamsuna
- Tandax
- Tarvexol
- Tavegyl
- Tavist - This combination medication is used to temporarily treat symptoms caused by the common cold , flu , allergies , or other breathing illnesses (such as sinusitis , bronchitis ). Decongestants help relieve stuffy nose, sinus , and ear congestion symptoms. Acetaminophen (APAP) is a non- aspirin pain reliever and fever reducer. Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. Therefore, do not use this product to treat cold symptoms ...
- Temazepam - WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death ( see WARNINGS and Drug Interactions ). ...
- Temol - Pharmacological action Acetaminophen is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetaminophen prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in...
- Tenaron
- Tenoxicam - Tenoxicam, an antiinflammatory agent with analgesic and antipyretic properties, is used to treat osteoarthritis and control acute pain. Indication: For the treatment of rheumatoid arthritis, osteoarthritis, backache, and pain.
- Tensin - Pharmacological action Spironolactone is a potassium, magnesium sparing diuretic. This medication is a competitive antagonist of aldosterone on the effect on distal nephron (competes for binding sites on cytoplasmic protein receptors, reduces the synthesis of permeases in the aldosterone-sensitive part of collecting tubules and distal tubules), increases the excretion of Na+, Cl- and water and reduces the excretion of K+ and urea, reduces the titratable acidity of urine. Increased diuresis...
- Terazosin - Terazosin is a selective alpha1-antagonist used for treatment of symptoms of benign prostatic hyperplasia (BPH). It also acts to lower blood pressure, so it is a drug of choice for men with hypertension and prostate enlargement. It works by blocking the action of adrenaline on smooth muscle of the bladder and the blood vessel walls. Indication: For the treatment of symptomatic BPH and mild to moderate hypertension. Terazosin, classified as a quinazoline, is similar to doxazosin and prazosin. As...
- Terazosine
- Terbifil
- Terbinafin
- Terbinafine - Terbinafine information Terbinafine is an antifungal drug used as athlete's foot medication. Terbinafine works like an antibiotic to treat fungal infections. Terbinafine indications This medicine is mainly indicated to treat fungal infections of the fingernails and toenails. Terbinafine may also be used for purposes not mentioned here. Terbinafine warnings This drug is classed as a FDA pregnancy category B drug and may cause severe side effects to an unborn baby. Consult with your...
- Terfenadine - In the U.S., Terfenadine was superseded by fexofenadine in the 1990s due to the risk of cardiac arrhythmia caused by QT interval prolongation. Indication: For the treatment of allergic rhinitis, hay fever, and allergic skin disorders. Terfenadine, an H1-receptor antagonist antihistamine, is similar in structure to astemizole and haloperidol, a butyrophenone antipsychotic. The active metabolite of terfenadine is fexofenadine.
- Ternelin
- Teronac
- Testosterone - DESCRIPTION TESTOPEL ® (testosterone pellets) are cylindrically shaped pellets 3.2mm (1/8 inch) in diameter and approximately 9mm in length. Each sterile pellet weighs approximately 78mg (75mg testosterone) and is ready for implantation. Androgens are steroids that develop and maintain primary and secondary male sex...
- Tetris
- TheraFlu Flu, Cold and Cough
- TheraFlu Flu, Cold and Cough Medicine
- Thiopental - A barbiturate that is administered intravenously for the induction of general anesthesia or for the production of complete anesthesia of short duration. It is also used for hypnosis and for the control of convulsive states. It has been used in neurosurgical patients to reduce increased intracranial pressure. It does not produce any excitation but has poor analgesic and muscle relaxant properties. Small doses have been shown to be anti-analgesic and lower the pain threshold. (From Martindale,...
- Thioridazine - A phenothiazine antipsychotic used in the management of psychoses, including schizophrenia, and in the control of severely disturbed or agitated behavior. It has little antiemetic activity. Thioridazine has a higher incidence of antimuscarinic effects, but a lower incidence of extrapyramidal symptoms, than chlorpromazine. (From Martindale, The Extra Pharmacopoeia, 30th ed, p618) Indication: For the treatment of schizophrenia and generalized anxiety disorder. Thioridazine is a trifluoro-methyl...
- Thiothixene - WARNING Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a...
- Thrombareduct
- Thycapzol
- Thyrex
- Thyrogen - Thyrotropin alfa belongs to the class of medications called human thyroid stimulating hormones. It is used with radioactive iodine to treat people with thyroid cancer who have had most or all of their thyroid gland removed. It is also used as an additional diagnostic tool, with or without radioactive iodine, for testing for thyroglobulin (Tg) in the blood in people with thyroid cancer. Thyrotropin alfa is a man-made hormone that acts the same way as the naturally-occurring thyroid...
- Ticlopidine - Ticlopidine is an effective inhibitor of platelet aggregation. The drug has been found to significantly reduce infarction size in acute myocardial infarcts and is an effective antithrombotic agent in arteriovenous fistulas, aorto-coronary bypass grafts, ischemic heart disease, venous thrombosis, and arteriosclerosis. [PubChem] Indication: Used to reduce the risk of thrombotic stroke (fatal or nonfatal) in patients who have experienced stroke precursors, and in patients who have had a completed...
- Tilidin N
- Tiligetic
- Tiligetic DP
- Timisol
- Timisol SDU
- Timolol - DESCRIPTION Betimol ® (timolol ophthalmic solution), 0.25% and 0.5%, is a non-selective beta-adrenergic antagonist for ophthalmic use. The chemical name of the active ingredient is (S)-1-[(1,1-dimethylethyl)amino]-3-[(4-(4-morpholinyl)-1,2,5-thiadiazol-3-yl]oxy]-2-propanol. Timolol hemihydrate is the levo isomer. Specific rotation is [α] 25 405nm =-16° (C=10% as the hemihydrate form in 1N HCl). The molecular...
- Tirlor
- Tirotax
- Tizanidine - Tizanidine is a short-acting drug for the management of spasticity. Tizanidine is an agonist at a2-adrenergic receptor sites and presumably reduces spasticity by increasing presynaptic inhibition of motor neurons. In animal models, tizanidine has no direct effect on skeletal muscle fibers or the neuromuscular junction, and no major effect on monosynaptic spinal reflexes. The effects of tizanidine are greatest on polysynaptic pathways. The overall effect of these actions is thought to reduce...
- Tobramycin - DESCRIPTION Tobramycin inhalation solution, USP is a tobramycin solution for inhalation. It is a sterile, clear, slightly yellow, non-pyrogenic, aqueous solution with the pH and salinity adjusted specifically for administration by a compressed air driven reusable nebulizer. The chemical formula for tobramycin, USP is C 18 H 37 N 5 O 9 and the molecular weight is 467.52. Tobramycin, USP is O -3-amino-3-deoxy-α-D-glucopyranosyl-(1→4)- O -[2,6-diamino-2,3...
- Toilax
- Tolazamide - TOLINASE Tablets contain tolazamide, an oral blood glucose lowering drug of the sulfonylurea class. Tolazamide is a white or creamy-white powderwith a melting point of 165° to 173° C. The solubility of tolazamide at pH 6.0 (mean urinary pH) is 27.8 mg per 100 mL. The chemical names for tolazamide are (1) Benzenesulfonamide, N -[[(hexahydro-1 H -azepin-1-yl) amino] carbonyl]-4-methyl-; (2) 1-(Hexahydro-1 H -azepin-1-yl)-3-( p -tolylsulfonyl)urea and its molecular weight...
- Tolbutamide - DESCRIPTION Tolbutamide is an oral blood-glucose-lowering drug of the sulfonylurea class. Tolbutamide is a pure, white, crystalline compound which is practically insoluble in water. The chemical name is benzenesulfonamide, N-[(butylamino)-carbonyl]-4-methyl-. Its structure can be represented as follows: M.W. 270.35 C 12 H 18 N 2 O 3 S Tolbutamide is supplied as...
- Tolmetin - A non-steroidal anti-inflammatory agent (anti-inflammatory agents, NON-steroidal) similar in mode of action to indomethacin. [PubChem] Indication: For the relief of signs and symptoms of rheumatoid arthritis and osteoarthritis, including the treatment of acute flares long-term management. Also for treatment of juvenile rheumatoid arthritis. Tolmetin is a nonsteroidal anti-inflammatory agent. Studies in animals have shown tolmetin to possess anti-inflammatory, analgesic and antipyretic activity....
- Tolmin
- Tolterodine - Tolterodine is an antimuscarinic drug that is used to treat urinary incontinence. Tolterodine acts on M2 and M3 subtypes of muscarinic receptors. Indication: For the treatment of overactive bladder (with symptoms of urinary frequency, urgency, or urge incontinence). Tolterodine is a competitive muscarinic receptor antagonist. Both urinary bladder contraction and salivation are mediated via cholinergic muscarinic receptors. After oral administration, tolterodine is metabolized in the liver,...
- Tonar
- Tonopan
- Topiramat
- Topiramate - DESCRIPTION Topiramate is a sulfamate-substituted monosaccharide. Topiramate tablets are available as 25 mg, 50 mg, 100 mg, and 200 mg circular tablets for oral administration. Topiramate is a white crystalline powder with a bitter taste. Topiramate USP is most soluble in alkaline solutions containing sodium hydroxide or sodium phosphate and having a pH of 9 to 10. It is freely soluble in acetone, chloroform, dimethylsulfoxide, and ethanol....
- Topotecan - WARNING: BONE MARROW SUPPRESSION Do not give Topotecan Injection to patients with baseline neutrophil counts less than 1,500 cells/mm 3 . In order to monitor the occurrence of bone marrow suppression, primarily neutropenia, which may be severe and result in infection and death, monitor peripheral blood counts frequently on all patients receiving Topotecan...
- Torasemid
- Torasemid Eco
- Torasis
- Torecan
- Torkol
- Tradorec
- Tramadol - Pharmacological action Tramadol Karnataka Antibiotics & Pharmaceuticals is an opioid analgesic, a derivative of cyclohexanol. It is non-selective agonist of mu-, delta- and kappa-receptors in the CNS. Tramadol is a racemate (+) and (-) of isomers (50% / 50%) which in various ways are involved in analgesic effects. The isomer (+) is a pure agonist opioid receptors, it has low tropism and has a pronounced selectivity for different subtypes of receptors. The isomer (-) inhibiting neuronal...
- Tramadol LP
- Tramadol Retard
- Tramagetic
- Tramagetic Brause
- Tramahexal
- Tran-Qil - Pharmacological action Lorazepam is an anxiolytic drug (tranquilizer), a derivative of benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, muscle relaxant central, antiemetic effect. The mechanism of the anxiolytic, sedative and hypnotic action is associated with increased inhibitory effect of GABA in the CNS. Anticonvulsant action, apparently in part due to increased presynaptic inhibition; inhibited the spread of epileptogenic activity arising in the...
- Trandolapril - WARNING: FETAL TOXICITY When pregnancy is detected, discontinue trandolapril as soon as possible. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. (See WARNINGS : Fetal Toxicity .) DESCRIPTION Trandolapril is the ethyl ester prodrug of a nonsulfhydryl...
- Tranexamic Acid - RECENT MAJOR CHANGES Contraindications ( 4.1 ) 10/2013 Warnings and Precautions ( 5.1...
- Tranquase
- Transacalm
- Trasicor
- Trazodone - A serotonin uptake inhibitor that is used as an antidepressive agent. It has been shown to be effective in patients with major depressive disorders and other subsets of depressive disorders. It is generally more useful in depressive disorders associated with insomnia and anxiety. This drug does not aggravate psychotic symptoms in patients with schizophrenia or schizoaffective disorders. (From AMA Drug Evaluations Annual, 1994, p309) Indication: For the treatment of depression. Trazodone is an...
- Tremax
- Trepress
- Tres
- Triamcinolone - A glucocorticoid given, as the free alcohol or in esterified form, orally, intramuscularly, by local injection, by inhalation, or applied topically in the management of various disorders in which corticosteroids are indicated. (From Martindale, The Extra Pharmacopoeia, 30th ed, p739) Indication: For the treatment of perennial and seasonal allergic rhinitis. Triamcinolone and its derivatives are synthetic glucocorticoids that are used for their antiinflammatory or immunosuppressive properties.
- Triami
- Triaminic DM
- Triaminic DM Decongestant
- Triaminic DM Plus Decongestant
- Triaminic DM-D
- Triaminic Decongestant and Expectorant
- Triaminic Expectorant DH
- Triaminic Night Time Rub
- Triaminic SR
- Triaminicol - This combination medication is used to treat symptoms caused by the common cold , flu , allergies , hay fever, or other breathing illnesses (e.g., sinusitis , bronchitis ). Dextromethorphan is a cough suppressant that affects a certain part of the brain (cough center), reducing the urge to cough. Decongestants help relieve stuffy nose symptoms. Antihistamines relieve watery eyes , itchy eyes/nose/throat, runny nose, and sneezing. Cough-and-cold products have not been shown to be...
- Triamtereen
- Triamtereen HCT
- Triamtereen; Epitizide
- Triamteren / HCT
- Triamteren Comp.
- Triamterene; Hydrochlorothiazide
- Trifluoperazine - A phenothiazine with actions similar to chlorpromazine. It is used as an antipsychotic and an antiemetic. [PubChem] Indication: For the treatment of anxiety disorders, depressive symptoms secondary to anxiety and agitation. Trifluoperazine is a trifluoro-methyl phenothiazine derivative intended for the management of schizophrenia and other psychotic disorders. Trifluoperazine has not been shown effective in the management of behaviorial complications in patients with mental retardation.
- Triflusal - Approved by the European Stroke Organization, triflusal is recommended as lone therapy for the secondary prevention of atheroembotic stroke. Triflusal appears to be equally effective with a better safety profile than acetylsalicylic acid plus dypridamole and clopidogrel alone based on a double blind, randomized TACIP and TAPIRSS trials. Indication: Prevention of cardiovascular events such as strokeAcute treatment of cerebral infarction, myocardial infarctionThromboprophylaxis due to atrial...
- Trijodthyronin
- Trimebutine - Trimebutine belongs to the class of medications called spasmolytics . It is used to treat irritable bowel syndrome (spastic colon). This condition is caused by overactive movements of the bowels. Trimebutine works by slowing down or normalizing the abnormal movements of the bowel. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this medication may not be used for all of the conditions...
- Trimethoprim - SPL UNCLASSIFIED SECTION To reduce the development of drug-resistant bacteria and maintain the effectiveness of trimethoprim tablets, USP and other antibacterial drugs, trimethoprim tablets, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Trimethoprim is a synthetic antibacterial available in tablet form for...
- Trimin - This combination medication is used to treat symptoms caused by the common cold , flu , allergies , hay fever, or other breathing illnesses (e.g., sinusitis , bronchitis ). Dextromethorphan is a cough suppressant that affects a certain part of the brain (cough center), reducing the urge to cough. Decongestants help relieve stuffy nose symptoms. Antihistamines relieve watery eyes , itchy eyes/nose/throat, runny nose, and sneezing. Cough-and-cold products have not been shown to be...
- Triminetta
- Trimipramin
- Trimoxazole
- Trimoxazole-BC
- Triominic
- Triregol
- Tuberol
- Tusapres
- Tussaminic C
- Tussaminic C Forte
- Tussaminic C Pediatric
- Tussaminic DH
- Ulceran
- Ulcoprotect
- Ulgarine
- Ultrazole
- Ulxit
- Unava
- Uniquin
- Urclar
- Urica - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Urihexal
- Uripurinol - Pharmacological action Allopurinol Laboratories is a medication that violates the synthesis of uric acid. This drug is a structural analog of hypoxanthine. It inhibits the enzyme xanthine oxidase, which is involved in the conversion of hypoxanthine to xanthine and xanthine to uric acid. This is due to decrease in the concentration of uric acid and its salts in body fluids and urine, which helps dissolve existing uric acid deposits and prevents their formation in tissues and kidney....
- Urizide
- Urobacid
- Uromitexan - Mesna is used to protect the bladder against some of the harmful effects of certain cancer medications known as oxazaphosphorines (e.g., cyclophosphamide, ifosfamide). After injection, mesna stays in the blood and is quickly moved to the kidney. Once in the kidney, it attaches to the byproducts of cancer medications that can cause harm to the bladder, making them harmless. Your doctor may have suggested this medication for conditions other than those listed in these drug information...
- Uromitexan Multidose
- Uxalun
- VX2
- Vacer
- Valacyclovir - Valacyclovir is used to treat infections caused by certain types of viruses. In children, it is used to treat cold sores around the mouth (caused by herpes simplex ) and chickenpox (caused by varicella zoster). In adults, it is used to treat shingles (caused by herpes zoster) and cold sores around the mouth. Valacyclovir is also used to treat outbreaks of genital herpes. In people with frequent outbreaks, this medication is used to reduce the number of future episodes. Valacyclovir is...
- Valproat
- Valproate de Sodium
- Vancocin - Vancomycin belongs to the group of medications known as antibiotics . It works by killing the bacteria that are causing the infection. The oral form is used to treat certain infections of the gastrointestinal tract. The intravenous (IV) form of this medication is used to treat other infections such as those involving the bones, lungs, blood, and heart. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well,...
- Vancocin CP
- Vancomycin - Antibacterial obtained from Streptomyces orientalis. It is a glycopeptide related to ristocetin that inhibits bacterial cell wall assembly and is toxic to kidneys and the inner ear. [PubChem] Indication: For the treatment of serious or severe infections caused by susceptible strains of methicillin-resistant (beta-lactam-resistant) staphylococci. Vancomycin is a branched tricyclic glycosylated nonribosomal peptide produced by the fermentation of the Actinobacteria species Amycolatopsis...
- Vancomycine
- Vartalon Complemento
- Vartalon Duo
- Vasotek I.V. - Enalapril information Enalapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Enalapril helps to keep raising blood pressure under control thereby reducing the risk factors of this disease. Since hypertension works out the heart muscles to cause early arterial failure, Enalapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- Vass
- Vastus
- Vegestabil
- Vegestabil Digest
- Veham-Sandoz
- Vehem
- Venlafaxin
- Venlafaxin ER Eco
- Venlafaxine - Suicidality and Antidepressant Drugs Antidepressants increased the risk compared to placebo of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults in short-term studies of Major Depressive Disorder (MDD) and other psychiatric disorders. Anyone considering the use of venlafaxine tablets or any other antidepressant in a child, adolescent; or young adult must...
- Venlafaxine LP
- Verahexal
- Verahexal KHK Retard
- Verahexal RR Retard
- Verahexal Retard
- Verapamil - A calcium channel blocker that is a class IV anti-arrhythmia agent. [PubChem] Indication: For the treatment of hypertension, angina, and cluster headache prophylaxis. Verapamil is an L-type calcium channel blocker that also has antiarrythmic activity. The R-enantiomer is more effective at reducing blood pressure compared to the S-enantiomer. However, the S-enantiomer is 20 times more potent than the R-enantiomer at prolonging the PR interval in treating arrhythmias.
- Verapamil LP
- Verapamil Retard
- Verpamil
- Vi-Medin
- Vibeden
- Vibradox
- Vibuzol
- Vimax
- Viskaldix
- Visken - Pindolol belongs to the class of medications called beta-blockers . It is used to treat high blood pressure and to prevent angina (chest pain). For treatment of high blood pressure, pindolol may be used alone or in combination with other medications that reduce high blood pressure, particularly thiazide diuretics (water pills). Pindolol works by decreasing the demands on the heart. Your doctor may have suggested this medication for conditions other than those listed in these drug...
- Visken + Brinaldix
- Viskenit
- Vita-Brachont
- Vitamin B12 - Pharmacological action Vitamin B12 refers to a group of water-soluble vitamins. It has high biological activity. Vitamin B12 is necessary for normal hematopoiesis (promotes maturation of erythrocytes). Involved in the processes of transmethylation, hydrogen transport, synthesis of methionine, nucleic acids, choline, creatine. Contributes to the accumulation in erythrocytes of compounds containing sulfhydryl groups. Has a beneficial effect on liver function and the nervous system. Activates...
- Vitamin C - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. [PubChem] Indication: Used to treat vitamin C deficiency, scurvy, delayed wound and bone healing, urine acidification, and in general...
- Vitamine B12
- Vitamine C - Pharmacological action Ascorbic acid (vitamin c) is essential for the formation of intracellular collagen, is required to strengthen the structure of teeth, bones, and the capillary walls. Vitamin C participates in redox reactions, the metabolism of tyrosine, converting folic acid into folinic acid, metabolism of carbohydrates, the synthesis of lipids and proteins, iron metabolism, processes of cellular respiration. Reduces the need for vitamins B1, B2, A, E, folic acid, pantothenic acid,...
- Vitamine E
- Vivasartan
- Vivasartan Plus
- Voriconazole - 1 INDICATIONS AND USAGE VFEND is indicated for use in patients 12 years of age and older in the treatment of the following fungal infections: VFEND is an azole antifungal indicated for use in the treatment of: Invasive aspergillosis ( 1.1 ) Candidemia (nonneutropenics) and disseminated candidiasis in skin, abdomen,...
- Vyrohexal - Pharmacological action Acyclovir Pharma is an antiviral agent. Thymidine kinase of virus-infected cells actively converts acyclovir through a series of sequential reactions in the mono-, di- and triphosphate of acyclovir. The latter interacts with the viral DNA polymerase, and embedded in DNA, which is synthesized for new viruses. Thus it is formed a "defective" viral DNA which leads to suppression of replication of new generations of viruses. This mediciine acyclovir is active against...
- Warfarin - Warfarin information Warfarin is an anti-coagulant or a medicine which helps in the thinning of the blood. Warfarin indications This medication is indicated for the reduction of blood clotting essential for the prevention of heart attacks, stroke and the blocking of arteries and veins. Warfarin may also be prescribed to treat other medical conditions aside from the ones mentioned above. Warfarin warnings Due to the anti clotting property of Warfarin Sanis Health, it should be...
- Xionil
- Xorim
- Xorimax
- Xylometazoline - A nasal vasoconstricting decongestant drug which acts by binding to the same receptors as adrenaline. It is applied as a spray or as drops into the nose to ease inflammation and congestion of the nasal passageways. It binds alpha-adrenergic receptors to activate the adrenal system which causes systemic vasoconstriction, thereby easing nasal congestion. Indication: It is used for treating nasal congestion and minor inflammation due to allergies or colds. Xylometazoline is a direct acting...
- Yohimbine - A plant alkaloid with alpha-2-adrenergic blocking activity. Yohimbine has been used as a mydriatic and in the treatment of impotence. It is also alleged to be an aphrodisiac. [PubChem] Indication: Indicated as a sympatholytic and mydriatic. Impotence has been successfully treated with yohimbine in male patients with vascular or diabetic origins and psychogenic origins. Yohimbine is an indolalkylamine alkaloid with chemical similarity to reserpine. Yohimbine blocks presynaptic alpha-2 adrenergic...
- Z-Dorm - Pharmacological action Zopiclone is a sleeping drug from group of cyclopyrrolone derivatives. This drug is "non benzodiazepine" agonist of benzodiazepine receptors. Zopiclone also has sedative, anxiolytic, muscle-relaxing center, anticonvulsant and amnesic properties. Like a derivative of benzodiazepine zopiclone enhances GABA-ergic processes in the brain, interacting with the benzodiazepine receptors, as a result of the increased sensitivity of GABA-receptors to the neurotransmitter....
- Z-Pam
- Zaditen - Ketotifen belongs to the classes of medications called antiallergics and asthma prophylactics. This medication is used in combination with other medications to treat mild allergic asthma in children. Ketotifen is an anti-allergy medication that helps to reduce asthma symptoms by reducing the body's response to allergens (substances that cause allergic reactions). These allergens can often trigger an acute asthma attack. Your doctor may have suggested this medication for conditions...
- Zaditen Infant
- Zaditen SRO
- Zafil
- Zaleplon - SPL UNCLASSIFIED SECTION SPL UNCLASSIFIED SECTION CIV Rx only DESCRIPTION Zaleplon is a nonbenzodiazepine hypnotic from the pyrazolopyrimidine class. The chemical name of zaleplon is N-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-N-ethylacetamide. Its empirical formula is C 17 H 15 N 5 O,...
- Zaprine
- Zepac
- Zetri
- Zibil
- Zilversulfadiazine
- Ziohex
- Ziprasidone - Ziprasidone (marketed as Geodon, Zeldox) was the fifth atypical antipsychotic to gain FDA approval (February 2001). Ziprasidone is Food and Drug Administration (FDA) approved for the treatment of schizophrenia, and the intramuscular injection form of ziprasidone is approved for acute agitation in schizophrenic patients. Ziprasidone has also received approval for acute treatment of mania associated with bipolar disorder. [Wikipedia] Indication: For the treatment of schizophrenia and related...
- Zocolip - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
- Zoldorm
- Zolerol - Pharmacological action Metronidazole is an anti protozoal agent. It is believed that the mechanism of action is associated with DNA damage-sensitive microorganisms. Active against Trichomonas vaginalis, Gardnerella vaginalis, Giardia lamblia, Entamoeba histolytica, and obligate anaerobic bacteria (including Bacteroides spp., Fusobacterium spp.). Aerobic bacteria are resistant to metronidazole. In combination with amoxicillin Metronidazole is active against Helicobacter pylori. It is...
- Zoloid - Pharmacological action Alprazolam is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine. This medication has anxiolytic, sedative, hypnotic, anticonvulsant, central muscle relaxant effect. The mechanism of action is to enhance the inhibitory effect of endogenous GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors located in the allosteric center of postsynaptic GABA-receptor activating...
- Zolpidem - Zolpidem is a prescription short-acting nonbenzodiazepine hypnotic that potentiates gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, by binding to benzodiazepine receptors which are located on the gamma-aminobutyric acid receptors. Zolpidem is used for the short-term treatment of insomnia. It works quickly (usually within 15 minutes) and has a short half-life (2-3 hours). It is classified as an imidazopyridine. As an anticonvulsant and muscle relaxant, the beneficial effects...
- Zolpihexal
- Zoltrim
- Zoltrim Forte
- Zonisamide - DESCRIPTION Zonisamide capsule is an antiseizure drug chemically classified as a sulfonamide and unrelated to other antiseizure agents. The active ingredient is zonisamide, 1,2-benzisoxazole-3-methanesulfonamide. The empirical formula is C 8 H 8 N 2 O 3 S with a molecular weight of 212.23. Zonisamide is a white powder, pKa = 10.2, and is moderately soluble in water (0.80 mg/mL) and 0.1 N HCl (0.50 mg/mL). The chemical structure is: ...
- Zopiclon - Pharmacological action Zopiclone is a sleeping drug from group of cyclopyrrolone derivatives. This drug is "non benzodiazepine" agonist of benzodiazepine receptors. Zopiclone also has sedative, anxiolytic, muscle-relaxing center, anticonvulsant and amnesic properties. Like a derivative of benzodiazepine zopiclone enhances GABA-ergic processes in the brain, interacting with the benzodiazepine receptors, as a result of the increased sensitivity of GABA-receptors to the neurotransmitter....
- Zopiclone - Pharmacological action Zopiclone is a sleeping drug from group of cyclopyrrolone derivatives. This drug is "non benzodiazepine" agonist of benzodiazepine receptors. Zopiclone also has sedative, anxiolytic, muscle-relaxing center, anticonvulsant and amnesic properties. Like a derivative of benzodiazepine zopiclone enhances GABA-ergic processes in the brain, interacting with the benzodiazepine receptors, as a result of the increased sensitivity of GABA-receptors to the neurotransmitter....
- Zoutoplossing - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Sodium Chloride fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- Zumablok - Pharmacological action Atenolol is a cardioselective beta1-blocker without intrinsic sympathomimetic activity. This medication has antihypertensive, antianginal and antiarrhythmic action. Atenolol reduces the stimulatory effect on the heart sympathetic innervation and circulating catecholamines. The hypotensive effect of this drug is associated with a decrease in minute volume of blood, decreased activity of the renin-angiotensin system (has a greater significance for patients with...
- Zumadiac
- Zumafib
- Zumafib Micro
- Zumaflox - Pharmacological action Ciprofloxacin is a broad-spectrum antimicrobial drug of fluoroquinolone group with bactericidal action. Inhibits DNA gyrase and inhibits the synthesis of bacterial DNA. Highly active against most gram-negative bacteria: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae. Ciprofloxacin is active against Staphylococcus spp. (including strains producing and not producing...
- Zumalin
- Zumatic
- Zumatram
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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