Pharma company: ranbaxy
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List of ranbaxy products:
- 30 Plus
- Abac
- Abzorb - Pharmacological action Abzorb 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. Abzorb 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 vaginalis. ...
- 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,...
- Acetaminophen - 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...
- 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...
- Acetaminophen; Codeine N3
- 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...
- Acyclovir - 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...
- Adco-Amoclav
- Adco-Ciprin - Pharmacological action Adco-Ciprin 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. Adco-Ciprin is active against Staphylococcus spp. (including strains producing and not producing...
- Adheb
- Aeromist
- Afidil
- Airlukast
- Alapren - Alapren information Alapren is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Alapren 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, Alapren stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors, Alapren...
- Alfuzosine
- Alfuzosine L.P.
- Allerfen
- 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....
- 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...
- Altiva
- Altiva-D
- Altraflam-P
- Ambroxit
- Amilide
- 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...
- 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...
- Amlodipinmaleat
- Amobarbital; Secobarbitol
- Amoxicilin; Clarithromycin; Omeprazole
- Amoxicilinum; Clavulanicum Acidum
- 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; Clavulanate
- Amoxicilline
- Amoxicilline; Acide Clavulanique
- Amoxicilline; Acide Clavulanique Adultes
- Amoxicilline; Acide Clavulanique Enfants
- Amoxicilline; Acide Clavulanique Nourrissons
- Amoxiclav
- Amoxy + Clav Potas Com
- Amoxy Clav
- Amoxycillin - 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...
- Amoxycillin; Clavulanic Acid
- Amytal
- Angitrit
- Aprelief
- Arbil
- Aripra-MT
- Artagen - 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...
- Aspacardin
- Aspent
- Aspent-M
- Aspenter
- 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...
- 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...
- Attafur
- Aventyl - Nortriptyline belongs to the group of medications known as tricylic antidepressants . It is used to treat depression. It works in the central nervous system to elevate the mood of people with depression. It is believed to work by affecting the balance of natural chemicals (called neurotransmitters ) 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...
- Avessa
- Avessa Rheo
- Aviranz
- Aviro-Z
- Avirodin
- Avocomb
- Avocomb-E
- Avocomb-N
- Avolam - Lamivudine information Lamivudine is an anti-HIV treatment in the class of drugs called Nucleoside Reverse Transcriptase Inhibitors (NRTIs). The body breaks down these drugs into chemicals that stop HIV from infecting uninfected cells in the body, but they do not help cells that have already been infected with the virus. This product is an important part of combination anti-HIV treatment. Lamivudine inhibits the reproduction of viruses in the body. Lamivudine warnings Before taking the...
- Avostav
- 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...
- Azithromycine
- Azostat
- Bacqure
- Bacticlor
- Baxmune
- Beclamethazone
- Beclamethazone Easyhaler
- 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: ...
- Besquil - Pharmacological action Besquil 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...
- Bestinem
- Betaclav
- 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...
- 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)...
- Betheran
- 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...
- 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...
- Brustan
- Brustin
- 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
- 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...
- Calchan - 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...
- Calchew
- Calcidif
- Calcium Vitamine D3
- Calibs
- Calmpose
- Caluran - 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...
- Candesar
- Candesar-H
- Candesartan - Candesartan is an angiotensin-receptor blocker (ARB) that may be used alone or with other agents to treat hypertension. It is administered orally as the prodrug, candesartan cilexetil, which is rapidly converted to its active metabolite, candesartan, during absorption in the gastrointestinal tract. Candesartan lowers blood pressure by antagonizing the renin-angiotensin-aldosterone system (RAAS); it competes with angiotensin II for binding to the type-1 angiotensin II receptor (AT1) subtype and...
- Capsidol
- Capsola Medi
- Capsola Plus
- 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 Comp
- Carbilev
- 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...
- Cascor
- Cascor XL
- Casera
- Caslot - Caslot information Caslot 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. Caslot indications This medication is used primarily in treating hypertension or high blood pressure. Caslot warnings Taking Caslot may not be advisable if you have any of the following conditions: asthma heart problems such as low blood pressure, slow heart rate,...
- Caverta
- Cecnoin
- Cefachlor
- 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. ...
- 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...
- Cefdiel
- Cefditran
- 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...
- 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...
- Ceftop
- 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 ...
- Cefuroximaxetil
- 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...
- Celen
- Celica - 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...
- Cephalexin - 1 INDICATIONS & USAGE Cephalexin is a cephalosporin antibacterial drug indicated for the treatment of the following infections caused by susceptible isolates of designated bacteria: Respiratory tract infection ( 1.1 ) Otitis media ( 1.2 ) ...
- Cepocor
- Cepodem
- Cerestar
- Ceriton
- Ceroxim
- Ceroxim-XP
- Ceruvin
- Ceruvin-A
- 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 ...
- Cheri 4 Flu
- Chericof Cough Formula
- Chericof Lozenges
- Chericof Sofgels
- Chericold
- Cheripex
- Chew-E
- Children's Cetirizine Allergy
- Children's Cetirizine Hives Relief
- Chloramsone
- Chlorgest - This combination product is used to treat symptoms caused by the common cold , flu , allergies , hay fever, or other breathing illnesses (e.g., sinusitis , bronchitis ). Decongestants help relieve stuffy nose symptoms. This product also contains a narcotic cough suppressant ( antitussive ) that affects a certain part of the brain , reducing the urge to cough. Antihistamines relieve watery eyes , itchy eyes/nose/throat, runny nose, and sneezing. Cough-and-cold products have not been...
- Chlorhydrate d'Amiloride; Hydrochlorothiazide
- Cibral
- Cifran
- Cifran CT
- Cifran OD
- Cifran-CT-H
- Cifran-OZ
- Cilanem
- Cilastatin; Imipenem
- Cilentra
- Ciproace - 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...
- 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 ). ...
- Ciprofloxacine
- Citalift
- 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...
- Citanz
- Clarithomycin
- 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...
- Clarithromycine
- Clarithromycinum
- Clavam
- Clavam Bid
- Cleft - 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 ...
- Clindamycin - ZydaClin™ (clindamycin) Oral Drops liquid For Use in Dogs & Cats Equivalent to 25 mg per mL clindamycin ...
- Clomin
- 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....
- CloraCEF
- CloraCEF DS
- 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...
- Closcript - 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...
- Cloxil
- Co-Amoxyclav
- Coamoxyclav
- Cobese
- 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...
- Cohero
- Colcibra - Celecoxib information Celecoxib is a NSAIDs medicine (Non-steroidal anti inflammatory drug). As a NSAID drug, Celecoxib fights against inflammation, pain or swelling by reducing the amount of substances that cause them. Celecoxib indications This medication is usually prescribed to patients who suffer from Stiffness, pain or inflammation which may accompany Osteoarthritis or rheumatoid arthritis. Celecoxib helps ease these symptoms while also decreasing the amount of polyps from your...
- Coldact Broncho
- Coldact Flu Plus
- Colorex
- Conderm
- Contiflo Icon
- Contiflo OD
- Contiflo-D
- Conviron Forte
- Conviron-TR
- Coriem XL
- Corpril - 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...
- Corpril-AM
- Cotuss - Guaifenesin is used to treat coughs and congestion caused by the common cold , bronchitis , and other breathing illnesses. This product is usually not used for ongoing cough from smoking or long-term breathing problems (such as chronic bronchitis, emphysema ) unless directed by your doctor. Guaifenesin is an expectorant. It works by thinning and loosening mucus in the airways, clearing congestion, and making breathing easier. If you are self-treating with this medication , it is...
- Covamlo
- Covance
- Covance-D
- Covance-D CP
- Coviro
- Coviro-E
- Coviro-LS Kid
- Coviro-LS Kid DS
- Creval
- Crixan
- Crixan-OD
- Crolim
- Cronica
- Cronical
- Cutizone
- Cutizone-T
- 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...
- Cyproterone; Ethinylestradiol
- Dariten-OD
- Darvocet
- Defanac
- Degran
- Delta-K
- Deponit - This medication is used to prevent chest pain ( angina ) in people with a certain heart condition (coronary artery disease). Nitroglycerin belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enough blood . This drug works by relaxing and widening blood vessels so blood can flow more easily to the heart. This medication will not relieve chest pain once it occurs. It is also not intended to be used just before physical activities (such as ...
- Desval-ER
- Dewax
- Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
- Dextropropoxyphene; Paracetamol
- Dextropropoxyphene; Paracetamol; Cafeine
- Dibose
- 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 Sodique
- Difnal
- Difnal K - 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...
- Difnal OD - 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...
- 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 LP
- Diprovate Plus
- Disogram
- DisperMox - 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...
- Distaclor
- Distaclor MR
- Dolamide
- 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,...
- Dopezil
- 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...
- Duocad
- Dutagen
- Dutin
- E-Drops
- Easyhaler Beclometasone
- Easyhaler Budesonide
- 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
- Effcal
- Efferven
- Eflora
- Elcion
- Elcion CR
- Eleflox
- Eligard - Leuprolide is a medication that has been designed to mimic the actions of gonadotropin releasing hormone (GnRH or luteinizing hormone releasing hormone , LHRH), the hormone released from the hypothalamus gland in the brain. The hypothalamus uses GnRH to send messages to the pituitary gland in the brain, which then sends messages to the ovaries in women and the testicles in men, telling these organs to produce the sex hormones estrogen (in women) and testosterone (in men). Normally, GnRH...
- Elitox
- 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 Plus
- 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...
- Enhancin
- Enhancin-BD
- Enpott
- Enzymet
- 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...
- Esomeprazole - A highly effective inhibitor of gastric acid secretion used in the therapy of stomach ulcers and zollinger-ellison syndrome. The drug inhibits the H()-K()-ATPase (H()-K()-exchanging ATPase) in the proton pump of gastric parietal cells. [PubChem] Indication: For the treatment of acid-reflux disorders (GERD), peptic ulcer disease, H. pylori eradication, and prevention of gastroinetestinal bleeds with NSAID use. Esomeprazole is a compound that inhibits gastric acid secretion and is indicated in...
- 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 ...
- Etrobax
- Eurax - This medication is used to treat scabies . Scabies is a skin infection caused by mites that burrow into the skin. Irritation from the mites leads to severe itching and small bumps/ blisters filled with fluid/pus. Crotamiton works by killing the mites that cause scabies. It also helps relieve itching related to scabies and other skin conditions. Crotamiton belongs to two classes of drugs: scabicides and antipruritics.
- Excel
- Excel-M
- Exel
- Exel-G
- Exel-M
- Exelderm - Sulconazole is used to treat skin infections such as jock itch and ringworm. This medication is also used to treat a skin condition known as pityriasis ( tinea versicolor ), a fungal infection that causes a lightening or darkening of the skin of the neck, chest, arms, or legs. Sulconazole is an azole antifungal that works by preventing the growth of fungus.
- Exorex
- FBC
- FBC Plus
- Faktu
- 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...
- Faringodyl
- Faronem
- Fendin
- 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...
- 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...
- Fenules
- Fenules Complex
- Ferdek
- Fexadin
- Fexofenadine; 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: 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...
- 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...
- Flothin
- Flotral
- Floxaday
- Fluconasole - 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...
- Flucoric - 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...
- Fluhalt
- 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...
- Fluran - Pharmacological action Fluran 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...
- Fluzet
- Fluzet Capsules
- Fluzet X
- Foracet
- Formoterol - Formoterol is a long-acting (12 hours) beta2-agonist used in the management of asthma and/or chronic obstructive pulmonary disease (COPD). Inhaled formoterol works like other beta2-agonists, causing bronchodilatation through relaxation of the smooth muscle in the airway so as to treat the exacerbation of asthma. Indication: For use as long-term maintenance treatment of asthma in patients 6 years of age and older with reversible obstructive airways disease, including patients with symptoms of...
- Formoterol Easyhaler
- Fortwin
- Forzest
- 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 ...
- Fosinopril; 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, fosinopril and hydrochlorothiazide . Fosinopril belongs to a class of drugs known as ACE inhibitors . It works by relaxing blood vessels so that blood can flow more easily. Hydrochlorothiazide is a "water pill" (diuretic) and causes your body to get rid of extra salt and water. This...
- Fraxone
- FuciBET
- Fucidin
- Fucidin H - This medication is a combination product containing 2 medications: fusidic acid and hydrocortisone. It is used to treat mild to moderately severe atopic (allergic) dermatitis rashes that are infected by a particular bacteria ( Staph. aureus ). Fusidic acid belongs to the family of medications known as topical (applied to skin) antibiotics . It works by preventing the bacteria from reproducing, allowing the body's defenses to get rid of the existing bacteria. Hydrocortisone belongs to...
- Fulsed
- Furosemid - Pharmacological action Furosemid 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...
- Gabapantine - 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...
- 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...
- 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...
- Ganciclovir - THE CLINICAL TOXICITY OF GANCICLOVIR INCLUDES GRANULOCYTOPENIA, ANEMIA AND THROMBOCYTOPENIA. IN ANIMAL STUDIES GANCICLOVIR WAS CARCINOGENIC, TERATOGENIC AND CAUSED ASPERMATOGENESIS. GANCICLOVIR CAPSULES ARE INDICATED ONLY FOR PREVENTION OF CMV DISEASE IN PATIENTS WITH ADVANCED HIV INFECTION AT RISK FOR CMV DISEASE, FOR MAINTENANCE TREATMENT OF CMV RETINITIS IN IMMUNOCOMPROMISED PATIENTS, AND...
- Ganguard
- Garlic Pearls
- Gaszym
- Gembax
- Gentalene Plus
- Gentalene-C
- 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. ...
- Gentamicin Beta
- Gestid Suspension
- Gestid Tablets
- Gestodene; Ethinylestradiol
- Ginkocer
- 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...
- 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...
- Glimpid
- 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...
- Goldgesic
- Graftin
- Gramogyl Suspension
- Gramogyl Tablets
- Gramoneg
- Gramoneg-M
- Gramoneg-TN
- Gynostatum - 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...
- Halog - This medication is used to treat a variety of skin conditions (e.g., eczema , dermatitis, allergies , rash ). Halcinonide reduces the swelling, itching , and redness that can occur in these types of conditions. This medication is a strong corticosteroid.
- Halox-S
- Hemilift
- Hisnofil
- Histac
- Histac EVT - Pharmacological action Histac EVT 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...
- Histak
- Hizin
- Hyclean
- 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...
- Hydrocodone, Acetaminophen - This combination medication is used to relieve moderate to severe pain. It contains a narcotic pain reliever ( hydrocodone ) and a non-narcotic pain reliever (acetaminophen). Hydrocodone works in the brain to change how your body feels and responds to pain. Acetaminophen can also reduce a fever.
- ISMN
- 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...
- Indapamide LP
- Indinavir - A potent and specific HIV protease inhibitor that appears to have good oral bioavailability. [PubChem] Indication: Indinavir is an antiretroviral drug for the treatment of HIV infection. Indinavir is a protease inhibitor with activity against Human Immunodeficiency Virus Type 1 (HIV-1). Protease inhibitors block the part of HIV called protease. HIV-1 protease is an enzyme required for the proteolytic cleavage of the viral polyprotein precursors into the individual functional proteins found in...
- Invoril
- Invozide
- Isoket
- Isoket IV
- Isoptin SR - Verapamil belongs to the class of medications called calcium channel blockers . It is used for the treatment of high blood pressure , certain abnormal heart rhythms, and angina (chest pain). It works to control blood pressure and reduce the number of angina attacks by relaxing blood vessels. It also helps to normalize heart rhythms. Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. As well, some forms of this...
- 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: ...
- Isotretinoin - DO NOT GET PREGNANT CONTRAINDICATIONS AND WARNINGS Isotretinon
- Keflex - Cephalexin is an antibiotic that belongs to the family of medications known as cephalosporins. It is used to treat certain types of bacteria infections. Cephalexin is most often used to treat infections of the throat, skin, ear, bladder, respiratory tract, and bone. It works by killing the bacteria 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...
- Keflor
- Keflor CD
- Keflor MR
- Kefloxin
- Kenalog - This medication is used in a variety of conditions such as allergic disorders, arthritis , blood diseases, breathing problems , certain cancers, eye diseases, intestinal disorders, collagen and skin diseases. Triamcinolone acetonide is known as a corticosteroid hormone (glucocorticoid). It works by decreasing your body's immune response to these diseases and reduces symptoms such as swelling.
- Ketanov
- 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 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....
- Ketozole
- Klabax
- 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...
- Lamivudine - Lamivudine information Lamivudine is an anti-HIV treatment in the class of drugs called Nucleoside Reverse Transcriptase Inhibitors (NRTIs). The body breaks down these drugs into chemicals that stop HIV from infecting uninfected cells in the body, but they do not help cells that have already been infected with the virus. This product is an important part of combination anti-HIV treatment. Lamivudine inhibits the reproduction of viruses in the body. Lamivudine warnings Before taking the...
- Lamivudine; Zidovudine - This product contains 2 drugs: lamivudine and zidovudine. It is used with other HIV medications to help control HIV infection. It helps to decrease the amount of HIV in your body so your immune system can work better. This lowers your chance of getting HIV complications (such as new infections, cancer ) and improves your quality of life. Both lamivudine and zidovudine belong to a class of drugs known as nucleoside reverse transcriptase inhibitors (NRTIs). Lamivudine/zidovudine is not a cure...
- 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...
- Laura
- Laxitab
- Lestric
- Levant
- 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) ...
- Levroxa - 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...
- Linea Oro Magnesio, Potassio e Vitamina C
- Linea Oro Melatonina
- Linea Oro Vitamina C, Zinco, Echinacea
- 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 Plus
- 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...
- 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; Simethicone
- 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 ...
- Loratadine Redidose
- Loratadine; Pseudoephedrine
- 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, ...
- 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...
- Lovir
- Lovire - 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...
- Loxof - Levofloxacin information Levofloxacin is type of drug that belongs to the group of medicines called antiepileptic drug. Levofloxacin indications This medication is indicated to control seizure. The precise way of how Levofloxacin works is not yet known. This medicine may also be used for purposes not mentioned here. Levofloxacin warnings This drug belongs in the FDA pregnancy category C. Levofloxacin may cause severe side effects to an unborn baby. Do not take Levofloxacin...
- Luci
- Luci-N
- Magnaspor
- Medsop
- Mefenix
- Megapime
- Melartin
- 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....
- Melubrin
- Metagyl - 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...
- 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 OD
- Metformin XR
- Metformine
- 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...
- Mianserine
- 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...
- Minoclin
- 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...
- Minoz - 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...
- Minoz-OD - 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...
- 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...
- Mobiswift-D
- Mobizox
- Mobrine-IR
- Moisturex
- Moisturex-AF
- 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...
- Moten
- Mox
- Mox BD
- Mox Kid
- Mox P
- Mox Redimix
- Moxclav
- Moxclav-BD
- Mylom
- Myopar
- Naproscript - 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 - 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...
- 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-Penotran
- Neupent AF - 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...
- Nevipan
- Nevirapine - WARNING: LIFE-THREATENING (INCLUDING FATAL) HEPATOTOXICITY and SKINREACTIONS HEPATOTOXICITY: Severe, life-threatening,and in some cases fatal hepatotoxicity, particularly in the first18 weeks, has been reported in patients treated with VIRAMUNE. Insome cases, patients presented with non-specific prodromal signs orsymptoms of hepatitis and progressed to hepatic failure. These...
- Niavas
- Niavas-D
- Nicardipine - A potent calcium channel blockader with marked vasodilator action. It has antihypertensive properties and is effective in the treatment of angina and coronary spasms without showing cardiodepressant effects. It has also been used in the treatment of asthma and enhances the action of specific antineoplastic agents. [PubChem] Indication: Used for the management of patients with chronic stable angina and for the treatment of hypertension. Nicardipine, a dihydropyridine calcium-channel blocker, is...
- Nicergoline - An ergot derivative that has been used as a cerebral vasodilator and in peripheral vascular disease. It has been suggested to ameliorate cognitive deficits in cerebrovascular disease. [PubChem] Indication: For the treatment of senile dementia, migraines of vascular origin, transient ischemia, platelet hyper-aggregability, and macular degeneration. Nicergoline is a potent vasodilator (improves brain blood flow). On the cerebral level it prompts a lowering of vascular resistance, an increase in...
- Nifedipin - 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 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...
- 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...
- Nificard - 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...
- Nifiran - 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...
- Nitrendipin
- Nitrocine - Nitroglycerin extended-release capsules are used to prevent chest pain ( angina ) in people with a certain heart condition (coronary artery disease). This medication belongs to a class of drugs known as nitrates. Angina occurs when the heart muscle is not getting enough blood . This drug works by relaxing and widening blood vessels so blood can flow more easily to the heart. This medication will not relieve chest pain once it occurs. It is also not intended to be taken just before...
- Nitrofurantoin Monohydrate / Macrocrystals
- Noctaderm
- Norazol
- Norbactin
- Norbactin-Z
- 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
- Norlon
- 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...
- Nupentin - 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...
- Occidal - 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.,...
- Ofloxacin OD - 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.,...
- Oframax
- Oframax Forte
- Olanex
- Olanex F
- Olanex Instab
- 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...
- Omeprazole - WARNINGS AND PRECAUTIONS Bone Fracture ( 5.3 ) 09/2010 WARNINGS AND PRECAUTIONS Diminished anti-platelet activity of clopidogrel ( 5.4 ) 01/2011 ...
- Omepreazole - 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...
- Omsulosin
- Ondansetron - Warnings and Precautions, ( 5.3 ) 09/2014 1 INDICATIONS AND USAGE ZUPLENZ is a 5-HT3 receptor antagonist indicated for: ...
- One Alpha C
- One-Alpha
- Opium - 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 . Opium belongs to a class of drugs known as narcotic pain relievers, but this medication acts mainly to slow the gut. 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...
- Orfiril
- Orfiril Long
- Orfiril Retard
- Oseltamivir - An acetamido cyclohexene that is a structural homolog of sialic acid and inhibits neuraminidase. [PubChem] Indication: Oseltamivir (Tamiflu) is for the treatment of uncomplicated acute illness due to influenza infection in patients 1 year and older who have been symptomatic for no more than 2 days. It is also used for the prophylaxis of influenza in adult patients and adolescents 13 years and older. Oseltamivir is an antiviral drug, a neuraminidase inhibitor used in the treatment and...
- Osonase
- Osovair
- Oxcarbazepine - Warnings and Precautions ( 5.4 ) 6/2014 Warnings and Precautions ( 5.8 ) 7/2014 1 INDICATIONS AND USAGE Trileptal is indicated for use as monotherapy or adjunctive therapy in the treatment of partial seizures in adults and as monotherapy in the treatment of partial seizures in children...
- Ozcef
- Oziclide
- Oziclide MR
- Ozvir - 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...
- PMS-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...
- PMS-Pravastatin - Pravastatin belongs to the family of medications known as HMG CoA reductase inhibitors ("statins"). It is used in addition to diet and exercise to lower high cholesterol levels. Pravastatin works by blocking an enzyme that is needed to make cholesterol in the liver. Therefore, less cholesterol is made and levels of cholesterol in the blood decrease. Lowering cholesterol levels in the blood has been shown to reduce the risks associated with heart disease, such as heart attack...
- Panixine Disperdose
- Pantoprazol
- 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...
- 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,...
- 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...
- Pedoc
- Pentazocine - The first mixed agonist-antagonist analgesic to be marketed. It is an agonist at the kappa and sigma opioid receptors and has a weak antagonist action at the mu receptor. (From AMA Drug Evaluations Annual, 1991, p97) Indication: For the relief of moderate to severe pain. Pentazocine is a potent analgesic which when administered orally in a 50 mg dose appears equivalent in analgesic effect to 60 mg (1 grain) of codeine. Onset of significant analgesia usually occurs between 15 and 30 minutes...
- Pentazocine; Naloxone - This product is used to treat moderate to severe pain. It contains 2 medications, pentazocine and naloxone. Pentazocine is a narcotic pain reliever (opiate-type). It acts on certain centers in the brain to give you pain relief. Naloxone helps to prevent misuse of this product. It blocks the effect of pentazocine and may cause withdrawal reactions if this product is dissolved and injected. Naloxone does not have any effect when taken by mouth.
- Pentoxi Retard
- Pentoxifyllin
- 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...
- Pepfiz
- Pepflux
- Pioglar
- Pioglar-G
- Pioglar-GF
- Pioglar-M
- Piracetam
- 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...
- 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,...
- Pravastatine
- Pravator
- 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...
- Provake
- Pylobact
- Pylobact AM
- Pylobact NEO
- Pylomox
- 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; 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, quinapril and hydrochlorothiazide . Quinapril belongs to a class of drugs known as ACE inhibitors . It works by relaxing blood vessels so blood can flow more easily. Hydrochlorothiazide (or "The thiazide diuretic") increases the amount of urine you make, removing extra water and salt from...
- RBX-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 ...
- Raciper
- Raciper IV
- Raciper SF
- Raciper-D
- Ragacin
- 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 Plus
- Ramiprilum - 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...
- Ramitren - 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...
- Ran-Acetaminophen 8 Hour - 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...
- Ran-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.
- Ran-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...
- Ran-Atorvastatin - Atorvastatin belongs to the group of medications known as HMG CoA reductase inhibitors ("statins"). It is used to treat people who have high cholesterol levels, including those people who have certain inherited cholesterol disorders. When you use this medication, you also need to make lifestyle changes, including switching to a diet low in fat and cholesterol, quitting smoking, and increasing the amount of exercise you do. Atorvastatin works by blocking an enzyme that is used to...
- Ran-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...
- Ran-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,...
- Ran-Ciproflox - Ciprofloxacin is an antibiotic that belongs to the family of medications known as quinolones. It is used to treat infections caused by certain bacteria. It is most commonly used to treat infections of the skin, sinuses, bone, lung, ear, abdomen, kidney, prostate, and bladder. It can also be used to treat some sexually transmitted infections (STIs), some forms of infectious diarrhea, and typhoid fever. The extended release form of ciprofloxacin is used to treat bladder and kidney...
- Ran-Ciprofloxacin
- Ran-Citalo - Citalopram belongs to a group of medications called selective serotonin reuptake inhibitors (SSRIs). It is used to treat depression. SSRIs improve depression by increasing the amount of serotonin (a neurotransmitter) in certain areas of the brain, which in turn improves the ability of the brain to transmit messages from one nerve cell to another. Although you may start feeling better within a few weeks of treatment, the full effects of the medication may not be evident until several...
- Ran-Citalopram
- Ran-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...
- Ran-Domperidone - Domperidone belongs to the group of medications called dopamine antagonists . It is used to treat slowed movement in the gastrointestinal tract associated with diabetes and gastritis (inflammation of the stomach lining). In these people, domperidone improves symptoms of nausea, vomiting, bloating, and feeling of fullness. Domperidone is also used to prevent stomach problems such as nausea and vomiting associated with certain medications used to treat Parkinson's disease. It works to...
- Ran-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,...
- Ran-Fentanyl Matrix Patch - 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...
- Ran-Fentanyl Transdermal System
- Ran-Fosinopril - Fosinopril belongs to the class of medications called ACE inhibitors . It is used to treat high blood pressure and congestive heart failure . It works by relaxing blood vessels and by helping the heart to pump blood that carries oxygen to the different parts of the body more efficiently. Fosinopril may be used in addition to digoxin or a thiazide diuretic or both in the treatment of congestive heart failure. Your doctor may have suggested this medication for conditions other than those...
- Ran-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...
- Ran-Imipenem-Cilastatin
- Ran-Irbesartan Hctz
- Ran-Lisinopril - Lisinopril belongs to a class of medications called ACE inhibitors . It is used to treat high blood pressure and congestive heart failure. It works by relaxing blood vessels and helping the heart to pump blood that carries oxygen to the different parts of the body more efficiently. It is also used immediately after a heart attack in order to reduce the risk of having another heart attack. Your doctor may have suggested this medication for conditions other than those listed in these drug...
- Ran-Lovastatin - Lovastatin belongs to the family of medications known as cholesterol-lowering medications . It is used in addition to diet and exercise to lower high cholesterol. It is also used to slow the progression of coronary atherosclerosis (hardening of the arteries in the heart). It works by blocking an enzyme that is needed to make cholesterol in the body. Less cholesterol is made, and cholesterol levels in the blood decrease. The medication usually takes about 2 to 6 weeks to have a...
- Ran-Metformin - 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...
- Ran-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...
- Ran-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...
- Ran-Pravastatin - Pravastatin belongs to the family of medications known as HMG CoA reductase inhibitors ("statins"). It is used in addition to diet and exercise to lower high cholesterol levels. Pravastatin works by blocking an enzyme that is needed to make cholesterol in the liver. Therefore, less cholesterol is made and levels of cholesterol in the blood decrease. Lowering cholesterol levels in the blood has been shown to reduce the risks associated with heart disease, such as heart attack...
- Ran-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....
- Ran-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...
- Ran-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...
- Ran-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 ...
- Ran-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...
- Ran-Tamsulosin - 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....
- Ran-Valsartan
- Ran-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....
- Ranamp
- Rancef
- Ranceph
- Rancif - 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...
- Rancil - 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.
- Ranclav
- Ranclosil
- Rancotrim
- Randoclin - 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...
- Ranfen - 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...
- Ranferon
- Ranferon-12
- Ranflocs
- Raniclor
- Ranitidin
- 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...
- Ranklav
- Ranlol - 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...
- Ranmoxy
- Ranopril - 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...
- Ranoxyl
- Ransim - 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...
- Ranthrocin
- Ranvir - 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...
- Ranzol
- Raxit - 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...
- Reflin
- Reftax
- Refzil-O
- Regan
- Remicron
- Remicron MR
- Renotens - 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...
- Respara
- Resporidex
- Revital
- Revital Calcium D3
- Revital Garlic Pearls
- Revital Ginkgo
- Revital Ginseng Plus
- Revital Liquid - This product is used to replace fluids and minerals (e.g., sodium, potassium ) lost due to diarrhea and vomiting . It helps prevent or treat the loss of too much body water ( dehydration ). Having the right amount of fluids and minerals is important for the normal functioning of the body.
- Revitalite
- Revitan
- Rexpar
- Rheolin - 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...
- Rheoran SF
- Rheoran SF Rheocaps
- Riconia Silver
- Riconia Syrup
- Riconia Tablet
- Riconia-G
- Rimacid
- Rimacillin - Pharmacological action Ampicillin is an antibiotic of semisynthetic broad-spectrum penicillin group. This medication has a bactericidal effect by suppressing the synthesis of bacterial cell walls. Ampicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (with the exception of strains producing penicillinase), Streptococcus spp., Enterococcus spp., Listeria monocytogenes; aerobic gram-negative bacteria: Neisseria gonorrhoeae, Neisseria meningitidis, Escherichia coli,...
- Rimafen - 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...
- Rimapam
- Rimapurinol - 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....
- Rimoxallin
- Riomet - Metformin is used with a proper diet and exercise program and possibly with other medications to control high blood sugar. It is used in patients with type 2 diabetes (non- insulin -dependent diabetes ). 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. Metformin works by helping to restore your body's proper response to the...
- Riomet OD
- Riomet-G
- 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 ...
- Rivastigmine - 1 INDICATIONS AND USAGE EXELON PATCH is an acetylcholinesterase inhibitor indicated for treatment of: Mild, moderate, and severe dementia of the Alzheimer’s type (AD). ( 1.1 ) Mild to moderate dementia associated with Parkinson’s disease (PDD). ( 1.2 ) SPL UNCLASSIFIED...
- Roburol
- Rodera
- Roles
- Roles-IT
- Roles-SF
- Roletra
- Roletra MDT
- Roletra-D
- Roliflo-OD
- Roliten
- Romesec - 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...
- Romexyl - 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...
- Romilast
- Rosatin
- Roscillin
- Roscilox
- Rosuvas - Rosuvastatin is used along with a proper diet to help lower "bad" cholesterol and fats (such as LDL , triglycerides ) and raise "good" cholesterol (HDL) in the blood . It belongs to a group of drugs known as " statins ." It works by reducing the amount of cholesterol made by the liver . Lowering "bad" cholesterol and triglycerides and raising "good" cholesterol decreases the risk of heart disease and helps to prevent strokes and heart attacks . In addition to eating a proper diet...
- Rotram
- Rovacor
- Roxithro
- 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
- Rozidal - Rozidal information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Rozidal 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. Rozidal can also be used for treating other disorders or as a complementary drug. Rozidal warnings In order to...
- 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...
- Salbutamol Easyhaler
- Salceryl
- Saltamol
- Salza Liquid
- Salza Tablets
- Sebifin - 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...
- Secobarbital - Secobarbital (marketed by Eli Lilly and Company under the brand names SeconalВ® and Tuinal) is a barbiturate derivative drug. It possesses anaesthetic, anticonvulsant, sedative and hypnotic properties. In the United Kingdom, it was known as Quinalbarbitone. Indication: For the Short-term treatment of intractable insomnia for patients habituated to barbiturates Secobarbital, a barbiturate, is used for the induction of anesthesia prior to the use of other general anesthetic agents and for...
- Seconal - This medication is used to calm you just before surgery. Secobarbital belongs to a class of drugs known as barbiturate hypnotics. It works by affecting certain parts of the brain to calm you.
- Selzic
- Serlife
- Serlift
- 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...
- Sibutramine - Sibutramine (trade name Meridia in the USA, Reductil in Europe and other countries), usually as sibutramide hydrochloride monohydrate, is an orally administered agent for the treatment of obesity. It is a centrally acting stimulant chemically related to amphetamines. Sibutramine is classified as a Schedule IV controlled substance in the United States. In October 2010, Sibutramine was withdrawn from Canadian and U.S. markets due to concerns that the drug increases the risk of heart attack and...
- Silverex
- Simovotin
- Simvastat - 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...
- 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...
- Simvor - 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...
- Simvotin - 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...
- Sinopren - 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...
- Sobrium - Pharmacological action Sobrium is a sleeping drug from the group of imidazopyridine, specific agonist of omega1-receptors in CNS. It shortens the time to sleep, reduces the number of nighttime awakenings, increased sleep duration and improves its quality. This medication extends phase II of sleep, phases III and IV of deep sleep, does not affect the duration of REM sleep. Zolpidem characterized also by a central muscle relaxant and anticonvulsant effects. Pharmacokinetics After oral...
- Socalm
- Socrit
- Soliten
- Sorest
- 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...
- Sotret - This medication is used to treat severe cystic acne (also known as nodular acne) that has not responded to other treatment (e.g., benzoyl peroxide or clindamycin applied to the skin or tetracycline or minocycline taken by mouth). It belongs to a class of drugs known as retinoids. It works by decreasing facial oil (sebum) production. High amounts of sebum can lead to severe acne. If left untreated, severe acne may cause permanent scarring.
- Sovical Liquid
- Sovical Pinacolada
- Sovical Tablets
- Sovical-L Liquid
- Sovical-L Tablets
- Sovical-W
- Spasril
- Spectra
- Spiramycine; Metronidazole
- 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 ...
- Sporicef
- Sporidex
- Sporidex AF
- Sporidex Forte
- Sporidex Redimix
- Starval
- Statum - 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...
- Statum B
- Statum Plus
- Staxom
- Stecort-NM
- Storfib
- Storvas - 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...
- Storvas CP - 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...
- Storvas-AMF
- Storvas-EZ
- Sucral
- Sucralfate - DESCRIPTION Sucralfate is an α-D-glucopyranoside, β-D-fructofuranosyl-, octakis(hydrogen sulfate), aluminum complex. R = SO Al(OH) 3 2 Tablets for oral administration contain 1 g of sucralfate. Structural formula for sucralfate CLINICAL PHARMACOLOGY ...
- Sudhinol
- Sulbamp
- 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...
- Suncros
- Suncros-SPF
- Suprimox
- Suprimox-P
- Symbiva
- 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...
- 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...
- Taxcef
- Teczine
- Teczine Instab
- Tensotec
- Tentide
- 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...
- 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...
- Tetradox
- Texara Forte
- Theosal
- Theostan-CR
- Tibikit
- Tibikit Plus
- Tibirim
- Tibirim INH
- Tindol
- Tinibid-DS
- Tiniflox
- Tobitil
- 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....
- Toride
- Trambax
- Trexydin
- Trexyl
- 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...
- Triviro
- Triviro Kid
- Triviro Kid DS
- Triviro-ALZ
- Ulcaid
- Ultiron-TR
- Ultraflam
- Ultrazox
- Unichew
- Unimezol - 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...
- V-Letra
- Valganciclovir - Valganciclovir hydrochloride (Valcyte, manufactured by Roche) is an antiviral medication used to treat cytomegalovirus infections. As the L-valyl ester of ganciclovir, it is actually a prodrug for ganciclovir. After oral administration, it is rapidly converted to ganciclovir by intestinal and hepatic esterases. Indication: Valganciclovir is an antiviral medication used for the treatment of cytomegalovirus infections. Valganciclovir is an antiviral medication used to treat cytomegalovirus...
- Valproate de Sodium
- Valsartan - WARNING: USE IN PREGNANCY When used in pregnancy, drugs that act directly on the renin-angiotensin system can cause injury and even death to the developing fetus. When pregnancy is detected, Diovan should be discontinued as soon as possible. See WARNINGS: ...
- Vamlo
- Vaxigrip - This medication belongs to a group of medications known as vaccines. It is used to prevent influenza (the flu). Influenza is a common viral illness caused by 2 types of virus: influenza A and influenza B. Each year, different strains (new, slightly different versions of the virus) appear. Scientists predict which strains will be most likely for the coming year, and then these strains are used to make up the year's influenza vaccine. Each year's influenza vaccine contains 3 virus...
- Venla
- 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...
- 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.
- Veratide
- Vercef
- Vercef AF
- Vercef Distab
- Vercef MR
- Verorab
- Viro-ALZ
- Viro-Z
- Virocmb-E
- Virocomb
- Virocomb-E
- Virocomb-N
- Virodin
- Virol
- Virolam - Lamivudine information Lamivudine is an anti-HIV treatment in the class of drugs called Nucleoside Reverse Transcriptase Inhibitors (NRTIs). The body breaks down these drugs into chemicals that stop HIV from infecting uninfected cells in the body, but they do not help cells that have already been infected with the virus. This product is an important part of combination anti-HIV treatment. Lamivudine inhibits the reproduction of viruses in the body. Lamivudine warnings Before taking the...
- Virolans
- Virolis
- Virolis-E
- Virosine-DR
- Virostav
- Voglibose - Voglibose (INN and USAN) is an alpha-glucosidase inhibitor used for lowering post-prandial blood glucose levels in people with diabetes mellitus. It is made in India by Ranbaxy Labs and sold under the trade name Volix. [Wikipedia] Indication: For the treatment of diabetes. It is specifically used for lowering post-prandial blood glucose levels thereby reducing the risk of macrovascular complications. Voglibose, an alpha-glucosidase inhibitor, is a synthetic compound with potent and enduring...
- Volini
- Volini Gel
- Volini Spray
- Volinigel
- Volitra
- Volix
- Vorzu
- XPhil-Nu
- Xabine
- Xenid
- Xolaam
- Xtraban
- Xtragesic-A.F.
- Xtroz
- Yugard
- Zanlop
- Zanocin - 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.,...
- Zanocin-DS - 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.,...
- Zanocin-OD - 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.,...
- Zanocin-OZ
- Zanocin-TZ
- Zanocin-TZH
- Zeteze
- Zidovudine - WARNING: RISK OF HEMATOLOGICAL TOXICITY, MYOPATHY, LACTIC ACIDOSIS Hematologic Toxicity: Zidovudine tablets have been associated with hematologic toxicity including neutropenia and severe anemia, particularly in patients with advanced HIV-1 disease [see Warnings and Precautions (5.1) ]. Myopathy: Prolonged use...
- Zivator
- Zocef
- Zole
- Zole-F
- Zoleta
- Zolinox - 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....
- 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...
- 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: ...
- 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....
- Zorpex
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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