Pharma company: alphapharm
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List of alphapharm products:
- Accure - Pharmacological action Accure is a pharmaceutical agent for the treatment of acne. Contributes to the normalization of terminal cell differentiation, inhibits the hyperproliferation of the epithelium of excretory ducts of the sebaceous glands, the formation of detritus and makes it easier to evacuate. Due to this reduced production of sebum and facilitates its isolation, normal structure, decreasing the inflammatory reaction around the glands. For external and systemic application...
- Acebutolol - A cardioselective beta-adrenergic antagonist with little effect on the bronchial receptors. The drug has stabilizing and quinidine-like effects on cardiac rhythm as well as weak inherent sympathomimetic action. [PubChem] Indication: For the management of hypertension and ventricular premature beats in adults. Acebutolol is a cardioselective, beta-adrenoreceptor blocking agent, which possesses mild intrinsic sympathomimetic activity (ISA) in its therapeutically effective dose range. In general,...
- Acenorm
- Acimax - Pharmacological action Acimax 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. Acimax has a bactericidal effect on...
- Aclin
- Actilax
- Acyclo-V - Pharmacological action Acyclo-V Alphapharm 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...
- Adefin - Pharmacological action Adefin 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. Adefin dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This medicine...
- Adefin XL - Pharmacological action Adefin XL 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. Adefin XL dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This medicine...
- Akamin - Akamin information Akamin belongs to the group tetracycline, which is used to treat infections caused by bacteria. Akamin 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. Akamin stops the spread of infection and the remaining bacteria are killed by the immune system or eventually die. Akamin indications Akamin is indicated for the treatment different infections caused by bacteria...
- Alclox
- Aldazine
- Alepam - Pharmacological action Alepam is an anxiolytic drug (tranquilizer) from the group of benzodiazepine derivatives. This medication has anxiolytic and sedative effects. This drug possesses anticonvulsant and central muscle relaxant activity. The mechanism of action is associated with increased GABA-ergic processes in the brain. Mainly affects the activating reticular formation of the brain reducing the perception of impulses from sensory receptors in the limbic system and reducing the...
- Allereze
- Alodorm - Pharmacological action Alodorm is an hypnotic drug from benzodiazepines group. This medication has a marked sedative effect, anxiolytic, sedative, anticonvulsant and central muscle relaxant effect. The mechanism of action is associated with increased inhibitory effect of GABA in the CNS by increasing the sensitivity of the GABA-receptor mediator as a result of stimulation of benzodiazepine receptors. Alodorm increases the depth and duration of sleep. Sleep usually occurs in 20-40 minutes...
- Alphacin - Pharmacological action Alphacin is an antibiotic of semisynthetic broad-spectrum penicillin group. This medication has a bactericidal effect by suppressing the synthesis of bacterial cell walls. Alphacin 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,...
- Alphamox - Pharmacological action Alphamox 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 producing...
- Alphapress
- Alphapril - Alphapril information Alphapril is one of the most effective anti-hypertensive drugs in the market. Belonging to the angiotensin-converting-enzyme inhibitors (ACE inhibitors) category of drugs, Alphapril 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, Alphapril stands in the way and helps to keep your heart healthy, indirectly. Like all other ACE inhibitors,...
- 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...
- Alprim
- Alzene
- 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...
- Amizide
- Anagrelide - Anagrelide is a drug used for the treatment of essential thrombocytosis (ET; essential thrombocythemia). It also has been used in the treatment of chronic myeloid leukemia. [Wikipedia] Indication: For the treatment of patients with thrombocythemia, secondary to myeloproliferative disorders, to reduce the elevated platelet count and the risk of thrombosis and to ameliorate associated symptoms including thrombo-hemorrhagic events. Anagrelide is a drug used for the treatment of essential...
- Anpec
- Anpec SR
- Anpine - 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...
- Antenex
- Anthel
- Aratac
- Arima
- Arthrexin
- Asmol
- Asmol Expectorant
- Asmol Inhaler CFC-Free
- Asmol Uni-Dose
- Attenta
- Axit - This medication is used to treat advanced kidney cancer after previous treatment has not been effective. Axitinib works by slowing or stopping the growth of cancer cells. It belongs to a class of drugs known as tyrosine kinase inhibitors.
- Aylide
- 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 ...
- Barbloc
- Bicor
- Brenda-35 ED
- Butacort
- Butacort Aqueous
- C-Flox - Pharmacological action C-Flox Alphapharm 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. C-Flox Alphapharm is active against Staphylococcus spp. (including strains producing and not...
- Campral - Acamprosate belongs to the family of medications called alcohol abstinence aids. It is used as part of a comprehensive alcohol dependence treatment program that includes counselling. Acamprosate is used by people who are alcohol-dependent to help them keep from drinking alcohol after they have stopped. It is thought to work by restoring the balance of chemicals in the brain that influence alcohol dependence. Your doctor may have suggested this medication for conditions other than those...
- Carbi
- Cardol - Pharmacological action Cardol is a glucocorticosteroid. Cardol inhibits the function of leukocytes and tissue macrophages. The migration of leukocytes in the area of inflammation. Impair the capacity of macrophages to phagocytosis and the formation of interleukin-1. Contributes to the stabilization of lysosomal membranes, thereby reducing the concentration of proteolytic enzymes in the field of inflammation. Decreases capillary permeability due to histamine release. Inhibits activity of...
- Celapram
- Cellulone
- Cholstat
- Cilostazol - WARNING: CONTRAINDICATED IN HEART FAILURE PATIENTS Cilostazol is contraindicated in patients with heart failure of any severity. Cilostazol and several of its metabolites are inhibitors of phosphodiesterase III. Several drugs with this pharmacologic effect have caused decreased survival compared to placebo in patients with class III-IV heart failure. ...
- 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...
- Clamoxyl
- Clamoxyl Duo
- Clamoxyl Duo Forte
- Clamoxyl Forte
- 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,...
- Clonea - 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...
- Codapane
- Codapane Forte
- Col
- Colese - This medication is used along with a proper diet and exercise to lower cholesterol in people with high levels of cholesterol in the blood . Lowering cholesterol decreases the risk of heart disease and helps prevent strokes and heart attacks . Colesevelam is also used along with a proper diet and exercise to lower high blood sugar in people with type 2 diabetes (non- insulin -dependent diabetes ). Controlling high blood sugar helps prevent kidney damage, blindness, nerve...
- Coras
- Corbeton
- Cyprone
- Dapa
- Dapa-Tabs
- Deptran
- Deralin
- Diabex
- Diabex Forte
- Diabex XR
- Diaformin
- 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...
- Distaph
- Dizole - 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...
- Doline
- Doxylin
- Duride
- E-Mycin - This medication is used to treat or prevent a wide variety of bacterial infections . Erythromycin is known as a macrolide antibiotic. It works by stopping the growth of bacteria. This antibiotic treats or prevents 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. OTHER USES: This section contains uses of this drug that are not listed in the approved...
- Eleva
- Endep - This medication is used to treat mental/mood problems such as depression. It may help improve mood and feelings of well-being, relieve anxiety and tension, help you sleep better, and increase your energy level. This medication belongs to a class of medications called tricyclic antidepressants. It works by affecting the balance of certain natural chemicals (neurotransmitters such as serotonin) in the brain . OTHER USES: This section contains uses of this drug that are not listed in the...
- EpiPen - Epinephrine belongs to a family of medications called sympathomimetics. These medications resemble chemicals that are normally found in our bodies and are released during stressful situations, such as when we are scared, anxious, or angry. Epinephrine is used for the emergency treatment of severe allergic reactions ( anaphylaxis ) to insect bites, insect stings, food, medication, as well as other allergens (e.g., latex). During a severe allergic reaction, blood pressure can become...
- EpiPen Jr.
- Erbitux - Cetuximab belongs to a group of medications called antineoplastics, or anticancer medications. It is used alone or in combination with another anticancer medication, irinotecan, to treat a certain type of colorectal cancer that has spread to other parts of the body (known as metastatic colorectal cancer) that has not responded to other specific anticancer medications. It is also used along with radiation therapy to treat a certain skin cancer (squamous cell carcinoma) located on the head...
- Escitalopram - Warnings and Precautions ( 5.2 ) 1/2017 ...
- Felodur
- Felodur ER
- Fenac - 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...
- Filpril
- 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...
- Flecatab
- 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...
- Flutamin
- 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...
- Gen-Fenofibrate
- Gen-Fenofibrate Micro
- Genox
- Glimel
- Glipizide - SPL UNCLASSIFIED SECTION For Oral Use DESCRIPTION GLUCOTROL (glipizide) is an oral blood-glucose-lowering drug of the sulfonylurea class. The Chemical Abstracts name of glipizide is 1-cyclohexyl-3-[[p-[2-(5-methylpyrazine-carboxamido)ethyl]phenyl]sulfonyl]urea. The molecular formula is C 21 H 27 N 5 O 4 S; the molecular weight is...
- Glucophage - 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...
- Glucovance - This combination medication is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes (non- insulin -dependent diabetes ). It may also be used with other diabetes medications. This product contains 2 medications. Glyburide belongs to the class of drugs known as sulfonylureas. It lowers blood sugar by causing the release of your body's natural insulin and by decreasing the amount of sugar that your liver makes. Metformin works by...
- Glyade
- Hi-Fluor
- Hydopa
- Hydrene
- Hypnodorm
- Hysone - This combination medication is used to treat a variety of skin conditions (e.g., eczema , fungal skin infections such as ringworm/ athlete's foot / jock itch ). This product contains 2 medications. Clioquinol (also known as iodochlorhydroxyquin) is an antibiotic that works by preventing the growth of fungus/bacteria. Hydrocortisone is a mild corticosteroid that works by reducing the swelling, redness, and itching that occurs in the affected skin. This medication should not be used in...
- Ibilex
- Imrest - 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....
- Indapamide - SPL UNCLASSIFIED SECTION 40-9191 Revised — November 2015 Rx Only DESCRIPTION Indapamide is an oral antihypertensive/diuretic. Its molecule contains both a polar sulfamoyl chlorobenzamide moiety and a lipid-soluble methylindoline moiety. It differs...
- Inza - 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...
- Ipratrin
- Ipratrin Adult Uni-Dose
- Ipratrin Uni-Dose
- Jezil - 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...
- KSR
- Kalixocin
- Kalma - 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...
- Kaluril
- Keflor
- Keflor CD
- Kinson
- Kripton
- Lamogine
- Lisodur - 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...
- Lovan
- Lumin
- Magicul
- Maxor - 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...
- Mefic
- Megafol
- Melizide
- 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;...
- Metomax
- Metrogyl - 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...
- Minax
- 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...
- Mobilis - 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...
- Mobilis D - 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...
- Monace
- Movox
- 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...
- Naxen - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Neosulf
- Noten - 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...
- Nufloxib
- 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...
- Optimol
- Pamacid
- 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...
- Paxam - 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,...
- Paxtine
- Pendine - 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...
- Pioglitazone - Pharmacological action Pioglitazone is an oral hypoglycemic agent, series of thiazolidinedione derivatives. Powerful and selective agonist of gamma-receptors, peroxisome proliferator-activated (PPAR-gamma). PPAR-gamma receptors are found in adipose and muscle tissues and liver. Activation of nuclear receptor PPAR-gamma modulates the transcription of several genes that are sensitive to insulin, involved in controlling glucose and lipid metabolism. This medicine reduces insulin resistance in...
- Placil
- Pramin
- Presolol
- Pressin
- Progout - 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....
- Quinbisul
- Quinsul
- QuitX
- Rafen - 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...
- Rani 2
- Recofol
- Resprim
- Resprim Forte
- Rimycin
- Roximycin
- Selegiline - Pharmacological action Selegiline is an almost near-to-white crystalline powder that is round, convex, scored, and uncoated tablet. Selegiline is freely soluble in water. Selegiline is used to treat Parkinson's disease, a disease associated with low levels of dopamine in your brain. The question how really Selegiline works is not known but it is believed to prevent the breakdown of dopamine in your brain. After levedopa or carbidopa therapy begins to deteriorate, selegiline is usually...
- Selgene
- Sitriol
- Somidem
- Sorbidin
- Spiractin - Pharmacological action Spironolactone is a potassium, magnesium sparing diuretic. This medication is a competitive antagonist of aldosterone on the effect on distal nephron (competes for binding sites on cytoplasmic protein receptors, reduces the synthesis of permeases in the aldosterone-sensitive part of collecting tubules and distal tubules), increases the excretion of Na+, Cl- and water and reduces the excretion of K+ and urea, reduces the titratable acidity of urine. Increased diuresis...
- Staphlex
- Staphylex
- Tacidine
- Temaze
- Teril
- Testomet
- Thioprine
- Tilodene
- Tizanidine - Tizanidine is a short-acting drug for the management of spasticity. Tizanidine is an agonist at a2-adrenergic receptor sites and presumably reduces spasticity by increasing presynaptic inhibition of motor neurons. In animal models, tizanidine has no direct effect on skeletal muscle fibers or the neuromuscular junction, and no major effect on monosynaptic spinal reflexes. The effects of tizanidine are greatest on polysynaptic pathways. The overall effect of these actions is thought to reduce...
- Tramadol - Pharmacological action Tramadol Karnataka Antibiotics & Pharmaceuticals is an opioid analgesic, a derivative of cyclohexanol. It is non-selective agonist of mu-, delta- and kappa-receptors in the CNS. Tramadol is a racemate (+) and (-) of isomers (50% / 50%) which in various ways are involved in analgesic effects. The isomer (+) is a pure agonist opioid receptors, it has low tropism and has a pronounced selectivity for different subtypes of receptors. The isomer (-) inhibiting neuronal...
- Tramedo
- Triazolam - SPL UNCLASSIFIED SECTION Rx only DESCRIPTION Triazolam tablets contain triazolam, a triazolobenzodiazepine hypnotic agent. Triazolam is a white crystalline powder, soluble in alcohol and poorly soluble in water. It has a molecular weight of 343.21. The chemical name for triazolam is 8-chloro-6-(o-chlorophenyl)-1-methyl-4 H - s -triazolo-[4,3-α][1...
- Ulcol
- Ulcyte
- Uremide - 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...
- Valpro
- Xergic
- Zabel
- Zactin
- Zimstat - 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...
- 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: ...
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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