DRUGS & SUPPLEMENTS

Pharma company: sanis health

Name: Sanis health products
Creator: sdrugs.com
Published: 2021-11-11T10:10:10+00:00

List of sanis health products:

5-ASA
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,...
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...
Alendronate - Alendronate is a nitrogen-containing, second generation bisphosphonate. Bisphosphonates were first used to treat PagetвЂ™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...
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...
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...
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 drugвЂ™s vasodilatory effects involves pH-dependent inhibition of calcium influx via inhibition of smooth...
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...
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...
Azathioprine - SPL UNCLASSIFIED SECTION PRODUCT INFORMATION Rx only WARNING - MALIGNANCY Chronic immunosuppression with IMURAN, a purine antimetabolite increases risk of malignancy in humans. Reports of malignancy include post-transplant lymphoma and hepatosplenic T-cell lymphoma (HSTCL) in patients with inflammatory bowel disease....
Azithromycin - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azithromycin inhibits RNA-dependent protein synthesis of sensitive microorganisms. It active against gram-positive bacteria: Staphylococcus aureus, Streptococcus spp. (including Streptococcus pneumoniae, Streptococcus pyogenes group A); gram-negative bacteria: Haemophilus influenzae, Haemophilus parainfluenzae, Haemophilus ducreyi, Moraxella catarrhalis, Escherichia coli, Bordetella pertussis, Bordetella...
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 ...
Cilazapril - One of the angiotensin-converting enzyme inhibitors (ACE inhibitors) used for hypertension. It is a prodrug that is hydrolyzed after absorption to its main metabolite cilazaprilat. [PubChem] Indication: Cilazapril is an ACE inhibtor class drug used in the treatment of hypertension and heart failure. Cilazapril inhibits the production angiotensin II. By doing so, it decreases sodium and water reabsorption (via aldosterone) and it decreases vasoconstriction. The combined effect of this is a...
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...
Clonidine - Clonidine information Clonidine is a medicine that is meant to lower the patient's blood pressure. It achieves its purpose as it decreases the levels in which certain chemicals are found in the patient's blood. In this way, the veins and arteries are allowed to widen, enabling the heart to beat regularly. Clonidine indications Clonidine is normally used in the treatment of hypertension (also known as high blood pressure). But Clonidine can also be used for other purposes that have not...
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...
Diclofenac EC - 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 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...
Diclofenac SR - Pharmacological action NSAIDs, a derivative of phenylacetic acid, diclofenac has a pronounced anti-inflammatory, analgesic and mild antipyretic effect. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, which is a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Analgesic effect is due to two mechanisms: peripheral (indirectly, through suppression of prostaglandin...
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 ...
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...
Etidrocal
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...
Fenofibrate Micro - Fenofibrate 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 "fibrates." It works by increasing the natural substance (enzyme) that breaks down fats in the blood. Lowering triglycerides in people with very high triglyceride blood levels may decrease the risk of pancreas disease ( pancreatitis ). However, fenofibrate might not lower your...
Fenofibrate-S
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...
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...
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...
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...
Glyburide - DESCRIPTION Glyburide tablets USP contain glyburide, which is an oral blood-glucose-lowering drug of the sulfonylurea class. Glyburide is a white, crystalline compound. The chemical name for glyburide is 1-[[p-[2-(5-chloro-o-anisamido)ethyl]phenyl]-sulfonyl]-3-cyclohexylurea and the molecular weight is 493.99. It has the following structural formula: Molecular formula: C 23 H 28 ClN 3 O 5 S Each tablet,...
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...
Hydroxyurea - RECENT MAJOR CHANGES Indications and Usage, melanoma ( 1 ) Removed 7/2015 Indications and Usage, carcinoma of the ovary ( 1 ) Removed 7/2015 Dosage and Administration ( 2 ) 7/2015 Warnings and...
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...
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...
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 ...
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...
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, ...
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;...
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...
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...
Morphine SR
Nabumetone - SPL UNCLASSIFIED SECTION Rx Only Cardiovascular Risk NSAIDs Through out this package insert, the term NSAID refers to a non-aspirin non-steroidal anti-inflammatory drug. may cause an increased risk of serious cardiovascular thrombotic events,...
Naproxen - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
Naproxen DS - Naproxen DS information Naproxen DS is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen DS Sanis Health's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen DS indications Naproxen DS 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...
Naproxen EC - Naproxen EC information Naproxen EC is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen EC Sanis Health's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen EC indications Naproxen EC is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation...
Omeprazole - WARNINGS AND PRECAUTIONS Bone Fracture ( 5.3 ) 09/2010 WARNINGS AND PRECAUTIONS Diminished anti-platelet activity of clopidogrel ( 5.4 ) 01/2011 ...
Oxybutynin - Oxybutynin information This medication is used to relieve urinary and bladder difficulties, including frequent urination and inability to control urination. Oxybutynin also helps to decrease muscle spasms of the bladder. Oxybutynin warnings Before taking oxybutynin, tell your doctor and pharmacist if you are allergic to this medicine or any other drugs. Also tell your doctor and pharmacist what prescription and non prescription medications you are taking, especially diuretics ("water...
Oxycodone; Acetaminophen - This combination medication is used to help relieve moderate to severe pain. It contains a narcotic pain reliever ( oxycodone ) and a non-narcotic pain reliever (acetaminophen). Oxycodone works in the brain to change how your body feels and responds to pain. Acetaminophen can also reduce a fever.
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...
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 6вЂ™-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,...
Propafenone - An antiarrhythmia agent that is particularly effective in ventricular arrhythmias. It also has weak beta-blocking activity. The drug is generally well tolerated. [PubChem] Indication: Used to prolong the time to recurrence of paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms in patients without structural heart disease. Also used for the treatment of life-threatening documented ventricular arrhythmias, such as sustained ventricular tachycardia. Propafenone is a...
Quetiapine - Pharmacological action Quetiapine is an antipsychotic (neuroleptic) drug. This medication exhibits a high affinity for serotonin 5HT2-receptors compared with dopamine D1- and D2-receptors in the brain. Also quetiapine has a high affinity for histamine and alpha1-receptors and a less pronounced - to the alpha2-receptors. This drug has no affinity for the m-cholinergic receptors and benzodiazepine receptors. Quetiapine in the dose effectively blocking dopamine D2-receptors causing only weak...
Rabeprazole EC
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...
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 ...
Ropinirole - Dosage and Administration ( 2.3 ) 9/2016 Warnings and Precautions ( 5.7 , 5.9 ) 9/2016 1 INDICATIONS AND USAGE Ropinirole tablets are a non-ergoline dopamine agonist indicated for the treatment of Parkinson’s disease (PD) and moderate-to-severe primary Restless Legs Syndrome (RLS). ( 1.1 , 1.2 ) SPL UNCLASSIFIED...
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...
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...
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...
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...
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...
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....
Trazodone - A serotonin uptake inhibitor that is used as an antidepressive agent. It has been shown to be effective in patients with major depressive disorders and other subsets of depressive disorders. It is generally more useful in depressive disorders associated with insomnia and anxiety. This drug does not aggravate psychotic symptoms in patients with schizophrenia or schizoaffective disorders. (From AMA Drug Evaluations Annual, 1994, p309) Indication: For the treatment of depression. Trazodone is an...
Venlafaxine XR - Venlafaxine XR information Venlafaxine XR is a drug belonging to the antidepressant and anti-anxiety agents that aid in the control of depression and anxiety attacks. Venlafaxine XR indications This medicine is used to treat mental depression, as well as anxiety disorders and its symptoms. Venlafaxine XR warnings Before taking this antidepressant drug, determine if you are allergic to this medication or other components of Venlafaxine XR Sanis Health. Venlafaxine XR and pregnancy...
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...
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....

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The information was verified by Dr. Rachana Salvi, MD Pharmacology

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