Pharma company: genpharm
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List of genpharm products:
- Acid Concentrate BP RO4151
- Acid Concentrate BP RO9505
- Acid Concentrate BP RO9506
- Acid Concentrate BP RO9507
- Acid Concentrate BP RZ267C
- Acid Concentrate BP RZ278C
- Acid Concentrate BP RZ279C
- Acid Concentrate R04146
- Acid Concentrate R04938
- Acid Concentrate R04968
- Acid Concentrate R04969
- Acid Concentrate R04974
- Acid Concentrate R04975
- Acid Concentrate R04976
- Acid Concentrate R04981
- Acid Concentrate R04984
- Acid Concentrate RO4131
- Acid Concentrate RO4132
- Acid Concentrate RO4136
- Acid Concentrate RO4137
- Acid Concentrate RO4138
- Acid Concentrate RO4144
- Acid Concentrate RO4145
- Acid Concentrate RO4947
- Acid Concentrate RO4965
- Acid Concentrate RO4979
- Acid Concentrate RO4983
- Acid Concentrate RO9500
- Acid Concentrate RO9501
- Acid Concentrate RO9502
- Acid Concentrate RZ110C
- Acid Concentrate RZ111C
- Acid Concentrate RZ119C
- Acid Concentrate RZ123C
- Acid Concentrate RZ127C
- Acid Concentrate RZ144C
- Acid Concentrate RZ150C
- Acid Concentrate RZ153C
- Acid Concentrate RZ164C
- Acid Concentrate RZ167C
- Acid Concentrate RZ171C
- Acid Concentrate RZ183C
- Acid Concentrate RZ185C
- Acid Concentrate RZ186C
- Acid Concentrate RZ194C
- Acid Concentrate RZ195C
- Acid Concentrate RZ196C
- Acid Concentrate RZ198C
- Acid Concentrate RZ202C
- Acid Concentrate RZ203C
- Acid Concentrate RZ205C
- Acid Concentrate RZ206C
- Acid Concentrate RZ207C
- Acid Concentrate RZ208C
- Acid Concentrate RZ209C
- Acid Concentrate RZ210C
- Acid Concentrate RZ211C
- Acid Concentrate RZ212C
- Acid Concentrate RZ213C
- Acid Concentrate RZ247C
- Acid Concentrate RZ248C
- Acid Concentrate RZ249C
- Acid Concentrate RZ254C
- Acid Concentrate RZ264C
- Acid Concentrate RZ265C
- Acid Concentrate Ro4147
- Acid Concentrate Ro4148
- Acid Concentrate Ro9503
- Acid Concentrate Rz262C
- Acid Concentrate Rz271C
- Acid Concentrate Rz272C
- Acid Concentrate Rz274C
- Acid Concentrate Rz275C
- Acid Conentrate R04930
- Acid Reducer - Pharmacological action Acid Reducer 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...
- 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...
- Agpen
- Albuterol - Pharmacological action Albuterol Pharmaceuticals is a beta adrenoagonists with a predominant effect on beta2-adrenergic receptors (localized, particularly in the bronchi, myometrium, blood vessels). This medication prevents and reduces or eliminates bronchospasm, reduces the resistance in the airways, increases the vital capacity. It prevents the release of histamine, slow reacting substance from mast cells and factors chemotaxis of neutrophils. Compared with other drugs of this group has...
- Alendronate - Alendronate is a nitrogen-containing, second generation bisphosphonate. Bisphosphonates were first used to treat Paget’s disease in 1971. This class of medications is comprised of inorganic pyrophosphate analogues that contain non-hydrolyzable P-C-P bonds. Similar to other bisphosphonates, alendronate has a high affinity for bone mineral and is taken up during osteoclast resorption. Alendronate inhibits farnesyl pyrophosphate synthetase, one of the enzymes in the mevalonic acid pathway...
- Alpha-Lac
- 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...
- Amnesteem - 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.
- 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...
- Azathioprine - SPL UNCLASSIFIED SECTION PRODUCT INFORMATION Rx only WARNING - MALIGNANCY Chronic immunosuppression with IMURAN, a purine antimetabolite increases risk of malignancy in humans. Reports of malignancy include post-transplant lymphoma and hepatosplenic T-cell lymphoma (HSTCL) in patients with inflammatory bowel disease....
- 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: ...
- C-TRi T
- C-Tax P
- Calcium Chloride - SPL UNCLASSIFIED SECTION 1 Gram (100 mg/mL) Represents 27 mg (1.4 mEq) Ca ++ /mL Ansyr™ Plastic Syringe A...
- Ciprobiotic
- 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 ). ...
- 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...
- 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...
- Concentrated Haemodialysis Solution BP-RZ266C
- Concentrated Haemodialysis Solution BP-RZ270C
- Concentrated Haemodialysis Solution BP-RZ273C
- Dexiron - Iron dextran belongs to a class of medications known as iron supplements. It is an injectable form of iron that is used to treat iron-deficiency anemia when oral iron supplements cannot be taken or when oral iron supplements have not produced the needed results. Iron is important for the production of red blood cells. It helps red blood cells to carry oxygen to the various parts of the body. Your doctor may have suggested this medication for conditions other than the ones listed in...
- Divalproex - This medication is used to treat seizure disorders, certain psychiatric conditions (manic phase of bipolar disorder), and to prevent migraine headaches. It works by restoring the balance of certain natural substances (neurotransmitters) in the brain.
- Doxazosin - DESCRIPTION Doxazosin mesylate is a quinazoline compound that is a selective inhibitor of the alpha 1 subtype of alpha adrenergic receptors. The chemical name of doxazosin mesylate is 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(1,4-benzodioxan-2-ylcarbonyl) piperazine methanesulfonate. The molecular formula for doxazosin mesylate is C 23 H 25 N 5 O 5 • CH 4 O 3 S and the molecular weight is 547.6. It has the following structure: ...
- 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,...
- Etidronate
- 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 ...
- Etoposide - WARNINGS Etoposide should be administered under the supervision of a qualified physician experienced in the use of cancer chemotherapeutic agents. Severe myelosuppression with resulting infection or bleeding may occur. DESCRIPTION Etoposide (also commonly known as VP-16) is a semisynthetic derivative of...
- Euthyrox - Levothyroxine is used to treat an underactive thyroid ( hypothyroidism ). It replaces or provides more thyroid hormone, which is normally produced by the thyroid gland. Low thyroid hormone levels can occur naturally or when the thyroid gland is injured by radiation /medications or removed by surgery. Having enough thyroid hormone is important for maintaining normal mental and physical activity . In children, having enough thyroid hormone is important for normal mental and physical...
- 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...
- 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...
- 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...
- Flutamide - SPL UNCLASSIFIED SECTION Flutamide Capsules, USP Rx only Revised: July 2014 195814-2 Rx only WARNINGS: Hepatic Injury: There have been postmarketing reports of hospitalization...
- Fluvoxamine - Fluvoxamine is an antidepressant which functions pharmacologically as a selective serotonin reuptake inhibitor. Though it is in the same class as other SSRI drugs, it is most often used to treat obsessive-compulsive disorder.Fluvoxamine has been in use in clinical practice since 1983 and has a clinical trial database comprised of approximately 35,000 patients. It was launched in the US in December 1994 and in Japan in June 1999. As of the end of 1995, more than 10 million patients worldwide...
- 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...
- 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...
- Gen Glybe
- Gen 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...
- Gen-Acebutolol
- Gen-Acebutolol Type S
- Gen-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...
- Gen-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...
- Gen-Alprazolan - 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...
- Gen-Amantadine
- Gen-Amilazide
- Gen-Amiodarone
- Gen-Amoxicillin - 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...
- Gen-Anagrelide
- Gen-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...
- Gen-Azathioprine
- Gen-Baclofen - Pharmacological action Baclofen is a centrally acting muscle relaxant; GABA B -receptor agonist. It depresses mono-and polysynaptic reflexes presumably by reducing the release of excitatory amino acids (glutamate and aspartate) from the terminals which occurs as a result of stimulation of presynaptic GABA-receptors. This medication does not affect the transmission of impulses in the nerve-muscle synapses; reduces skeletal muscle tone; has a moderate analgesic effect. Pharmacokinetics ...
- Gen-Beclo
- Gen-Beclo AQ
- Gen-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...
- Gen-Bromazepam
- Gen-Budesonide AQ
- Gen-Buspirone
- Gen-Captopril
- Gen-Carbamazepine CR
- Gen-Cilazapril
- Gen-Cimetidine
- Gen-Ciprofloxacin
- Gen-Citalopram - 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...
- Gen-Clarithromycin
- Gen-Clindamycin
- Gen-Clobetasol
- Gen-Clomipramine
- Gen-Clonazepam - Pharmacological action Clonazepam is an antiepileptic drugs from the group of benzodiazepine derivatives. This medication has a pronounced anticonvulsant and central muscle relaxant, anxiolytic, sedative and hypnotic effects. Clonazepam strengthens the inhibitory effect of GABA on the transmission of nerve impulses. Anxiolytic effects of this drug is due to the influence on the amygdaloid complex of the limbic system and appears in reducing the emotional stress, reduce anxiety, fear,...
- Gen-Clozapine - Clozapine belongs to a family of medications called antipsychotics . It is used to treat schizophrenia when other medications are not effective. Schizophrenia is related to imbalances in certain brain chemicals such as dopamine. This medication helps to balance these chemicals. 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...
- Gen-Combo Sterinebs
- Gen-Cromoglycate
- Gen-Cromoglycate Sterinebs
- Gen-Cromolyn
- Gen-Cyclobenzaprine
- Gen-Cyproterone - Cyproterone belongs to a group of medications known as steroidal antiandrogens . It is used to treat advanced prostate cancer. Antiandrogens such as cyproterone block the effect of the hormone called testosterone . This causes a reduction in the production of testosterone in the testicles, which prostate cancer cells require for growth. 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...
- Gen-Diltiazem
- Gen-Diltiazem SR
- Gen-Divalproex
- Gen-Domperidone
- Gen-Doxazosin
- Gen-Enalapril
- Gen-Eti-Cal Carepac
- Gen-Etidronate
- Gen-Etodolac
- Gen-Famotidine
- Gen-Fenofibrate
- Gen-Fenofibrate Micro
- Gen-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...
- Gen-Fluoxetine
- Gen-Fluvoxamine
- Gen-Fosinopril
- Gen-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...
- Gen-Gemfibrozil - Gemfibrozil information Gemfibrozil is a drug which is usually prescribed along with a diet to people who have very high levels of serum triglycerides (triglycerides are fatty substances from the blood) and who are at a risk of developing pancreatitis (this is the inflammation of the pancreas). This medication may also be used in order to reduce the risk of developing coronary heart disease in people who have not responded to the other therapy options: weight loss, exercises, and diet and...
- Gen-Gliclazide
- Gen-Hydroxychloroquine
- Gen-Hydroxyurea
- Gen-Indapamide
- Gen-Ipratropium
- Gen-Lac
- Gen-Lamotrigine
- Gen-Leflunomide - Leflunomide information This medication, with the generic name of Leflunomide, is specially formulated to provide physical relief from inflammation, swelling, stiffness, and joint pain as caused by rheumatoid arthritis. Leflunomide acts by stopping the production of too much immune cells causing inflammation and swelling in the body. Leflunomide indications Leflunomide is prescribed to patients showing signs of rheumatism as listed below: Inflammation Swelling Stiffness Joint pain ...
- Gen-Lisinopril
- Gen-Lisinopril HCTZ
- Gen-Lovastatin
- Gen-Medroxy - Medroxyprogesterone belongs to the family of medications known as progesterones . Progesterones are female hormones. They are produced by the body and are necessary along with other hormones for normal female sexual development and for the regulation of the menstrual cycle during childbearing years. It reduces the effects of estrogen on tissues such as the endometrium (lining of the uterus) and the breast. Medroxyprogesterone has a variety of uses. It is used in addition to ...
- Gen-Meloxicam
- Gen-Metformin
- Gen-Metoprolol
- Gen-Metoprolol Type L
- Gen-Minocycline
- Gen-Minoxidil - Pharmacological action Minoxidil is a drugs for the treatment of hair loss. This medication has a stimulating effect on hair growth in men and women with androgenetic alopecia (male pattern baldness). The appearance of signs of hair growth observed after 4 months or more of taking the drug 2 times / day. The beginning and the severity of the effect may vary in different patients. After the abolition of minoxidil new hair growth stops, and after 3-4 months may restore the original...
- Gen-Mirtazapine
- Gen-Nabumetone
- Gen-Naproxen EC - 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...
- Gen-Nefazodone
- Gen-Nifedipine Extended Release - 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...
- Gen-Nitro
- Gen-Nizatidine
- Gen-Nortriptyline
- Gen-Oxybutynin
- Gen-Paroxetine
- Gen-Pindolol
- Gen-Pioglitazone
- Gen-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...
- Gen-Pravastatin
- Gen-Propafenone
- Gen-Quetiapine
- Gen-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...
- Gen-Ranitidine
- Gen-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 ...
- Gen-Salbutamol
- Gen-Salbutamol Sterinebs
- Gen-Salbutamol Sterinebs P.F.
- Gen-Selegiline
- Gen-Sertraline
- Gen-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...
- Gen-Sotalol
- Gen-Sumatriptan
- Gen-Tamoxifen
- Gen-Tamsulosin
- Gen-Temazepam
- Gen-Terbinafine
- Gen-Ticlopidine
- Gen-Timolol
- Gen-Tizanidine
- Gen-Topiramate
- Gen-Trazodone
- Gen-Triazolam
- Gen-Valproic
- Gen-Verapamil
- Gen-Verapamil SR
- Gen-Warfarin
- Gen-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....
- Guanfacine - DESCRIPTION Guanfacine hydrochloride is a centrally acting antihypertensive with α 2 -adrenoceptor agonist properties in tablet form for oral administration. The chemical name of guanfacine hydrochloride is N -Amidino-2-(2,6-dichlorophenyl) acetamide monohydrochloride and its molecular weight is 282.55. Its structural formula is: Guanfacine...
- Lamotrigine - WARNING: SERIOUS SKIN RASHES See full prescribing information for complete boxed warning. Cases of life-threatening serious rashes, including Stevens-Johnson syndrome and toxic...
- Levetiracetam - Levetiracetam information Levetiracetam is type of drug that belongs to the group of medicines called antiepileptic drug. Levetiracetam indications This medication is indicated to control seizure. The precise way of how Levetiracetam works is not yet known. This medicine may also be used for purposes not mentioned here. Levetiracetam warnings This drug belongs in the FDA pregnancy category C. Levetiracetam may cause severe side effects to an unborn baby. Do not take Levetiracetam...
- Levothyroxine - The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (monoiodotyrosine) and the coupling of iodotyrosines (diiodotyrosine) in the thyroglobulin. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form triiodothyronine which exerts a broad spectrum of stimulatory effects on cell metabolism. [PubChem] Indication: For use alone or in combination with antithyroid agents...
- 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 ...
- Lotor - 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...
- Lovastatin - DESCRIPTION Lovastatin, USP is a cholesterol lowering agent isolated from a strain of Aspergillus terreus . After oral ingestion, lovastatin, USP, which is an inactive lactone, is hydrolyzed to the corresponding β-hydroxyacid form. This is a principal metabolite and an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase. This enzyme catalyzes the conversion of HMG-CoA to mevalonate, which is an early and rate limiting step in the...
- 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....
- 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;...
- Methimazole - DESCRIPTION TAPAZOLE ® (Methimazole Tablets, USP) (1-methylimidazole-2-thiol) is a white, crystalline substance that is freely soluble in water. It differs chemically from the drugs of the thiouracil series primarily because it has a 5- instead of a 6-membered ring. Each tablet contains 5 or 10 mg (43.8 or 87.6 µmol) methimazole, an orally administered antithyroid drug. Each tablet also contains lactose monohydrate,...
- 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...
- Nizatidine - SPL UNCLASSIFIED SECTION Rx Only DESCRIPTION Nizatidine, USP is a histamine H2-receptor antagonist. Chemically, it is N -[2-[[[2-[(dimethylamino)methyl]-4-thiazolyl]methyl]thio]ethyl]- N’ -methyl-2-nitro-1,1-ethenediamine. The structural formula is as follows: Nizatidine, USP has the empirical...
- Novothyrox
- Omeprazole - WARNINGS AND PRECAUTIONS Bone Fracture ( 5.3 ) 09/2010 WARNINGS AND PRECAUTIONS Diminished anti-platelet activity of clopidogrel ( 5.4 ) 01/2011 ...
- Orofer Tablets
- Oxaprozin - WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS See full prescribing information for complete boxed warning. ...
- 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...
- Peptic Guard - Famotidine belongs to a class of medications called H 2 -antagonists . It is used to treat stomach and duodenal (intestinal) ulcers, gastroesophageal reflux disease (GERD), and conditions where too much stomach acid is secreted, such as Zollinger-Ellison syndrome. It works by reducing the amount of acid secreted by the stomach. The over-the-counter form of famotidine is used to treat conditions where a reduction of stomach acid is needed, such as acid indigestion, heartburn, or sour...
- Peptic Relief - This medication is used to treat occasional upset stomach , heartburn , and nausea . It is also used to treat diarrhea and help prevent travelers' diarrhea. It works by helping to slow the growth of bacteria that might be causing the diarrhea. This product should not be used to self-treat diarrhea if you also have a fever or blood /mucus in the stools. These could be signs of a serious health condition. Consult your doctor promptly for proper evaluation and treatment if you have these...
- Pindolol - T1999-39 89003701 Visken ® (pindolol) tablets, USP Rx only Visken ® (pindolol), a synthetic beta-adrenergic receptor blocking agent with intrinsic sympathomimetic activity is 1-(Indol-4-yloxy)-3-(isopropylamino)-2-propanol. Its structural formula is: Pindolol is a white to off-white odorless powder soluble in organic solvents and aqueous acids. Visken ® (pindolol)...
- 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...
- Potassium Chloride - SPL UNCLASSIFIED SECTION POTASSIUM CHLORIDE EXTENDED RELEASE TABLETS USP 20 mEq K Rx Only DESCRIPTION The Potassium Chloride Extended Release Tablets USP, 20 mEq product is an immediately dispersing extended release oral dosage form of potassium chloride containing 1500 mg...
- 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,...
- 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...
- Sabulin Inhaler - 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...
- 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...
- Sodium Bicarbonate - Enter section text here Active ingredient Purpose (in each tablet) Sodium bicarbonate 10 gr (650 mg) ....... Antacid Enter section text...
- Sodium Bicarbonate-Chloride Dry Concentrate
- Sodium Bicarbonate-Chloride Dry Concentrate R04955
- Sodium Bicarbonate-Chloride Liquid Concentrate RO4941
- 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...
- T-Vac
- 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...
- Ticlopidine - Ticlopidine is an effective inhibitor of platelet aggregation. The drug has been found to significantly reduce infarction size in acute myocardial infarcts and is an effective antithrombotic agent in arteriovenous fistulas, aorto-coronary bypass grafts, ischemic heart disease, venous thrombosis, and arteriosclerosis. [PubChem] Indication: Used to reduce the risk of thrombotic stroke (fatal or nonfatal) in patients who have experienced stroke precursors, and in patients who have had a completed...
- Venofer - This medicine is used to treat "iron-poor" blood ( anemia ) in people with long-term kidney disease. You may need extra iron because of blood loss during kidney dialysis . Your body may also need more iron if you use the drug erythropoietin to help make new red blood cells. Iron is an important part of your red blood cells and is needed to transport oxygen in the body. Many patients with kidney disease cannot get enough iron from food and require injections.
- Warfarin - Warfarin information Warfarin is an anti-coagulant or a medicine which helps in the thinning of the blood. Warfarin indications This medication is indicated for the reduction of blood clotting essential for the prevention of heart attacks, stroke and the blocking of arteries and veins. Warfarin may also be prescribed to treat other medical conditions aside from the ones mentioned above. Warfarin warnings Due to the anti clotting property of Warfarin Sanis Health, it should be...
- Zaleplon - SPL UNCLASSIFIED SECTION SPL UNCLASSIFIED SECTION CIV Rx only DESCRIPTION Zaleplon is a nonbenzodiazepine hypnotic from the pyrazolopyrimidine class. The chemical name of zaleplon is N-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-7-yl)phenyl]-N-ethylacetamide. Its empirical formula is C 17 H 15 N 5 O,...
- 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...
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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