Pharma company: g. streuli

List of g. streuli products:

• ASA - Pharmacological action ASA is a NSAIDs. It has anti-inflammatory, analgesic and antipyretic effect, and inhibits platelet aggregation. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid which is a precursor of prostaglandins which play a major role in the pathogenesis of inflammation, pain and fever. Reduction of prostaglandins (mainly E1) in the thermoregulation center leads to a decrease in body temperature due to...
• ASA-Tabs
• Acemucol
• Acetalgin - Pharmacological action Acetalgin is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetalgin prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in trauma,...
• Acetalgine - Pharmacological action Acetalgine is an analgesic-antipyretic. It has analgesic, antipyretic and weak anti-inflammatory action. The mechanism of action is associated with inhibition of prostaglandin synthesis, the predominant influence on the thermoregulation center in the hypothalamus, enhances heat transfer. Why is Acetalgine prescribed? Pain weak and moderate intensity of different genesis (including headache, migraine, toothache, neuralgia, myalgia, algomenorrhea; pain in trauma,...
• Acide Acetylsalicylique Comp Radix
• Acidum Folicum
• Aloinophen
• Amlovasc
• 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...
• Anaestalgin
• Angina MCC
• Anginol
• Antemin
• Antemin Comp.
• Antemin Compositum
• Antigestin
• Aphenylbarbit
• Atropinium Sulfuricum
• Baneopol
• Barbamin
• Baume Esco
• Baume Esco Forte
• Becotal
• Becotal Forte
• Bellafit N
• Bellagotin
• Bilivectan
• Bromocod N
• Bronchol
• Butadion
• Butaparin
• C-Calcium
• C-Calcium Forte
• C-D-Calcium
• Cetirizin
• Chloramon
• Chlorazin
• Chlorochin
• Chronocort
• Chronocorte
• Cinnageron - Pharmacological action Cinnarizine is a calcium channel blocker class IV with a predominant effect on the brain vessels, a derivative of piperazine. This medication improves cerebral, coronary and peripheral circulation. Cinnarizine violates the entrance of calcium ions into vascular smooth muscle cells. This drug lowers the tone of arteriolar smooth muscle, decreases the vasoconstrictor response to biogenic substances (epinephrine, norepinephrine, bradykinin). Cinnarizine reduces the...
• 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...
• Combacid N
• Corprilin
• Corpriretic
• Cortifluid N
• Cortisteron
• Cotalbex
• Cyclandelat
• Dentohexin
• Dentohexine
• Desamon
• Dexacortin
• Dexacortin-K - Pharmacological action Dexamethasone is a glucocorticosteroid. This medication Inhibits the function of leukocytes and tissue macrophages. Dexamethasone restricts the migration of leukocytes in the area of inflammation. This drug violates the ability of macrophages to phagocytosis and the formation of interleukin-1. Dexamethasone decreases capillary permeability caused by histamine release. This medicine inhibits the activity of fibroblasts and collagen formation. Dexamethasone inhibits...
• Dexamin
• Dexolan
• Digoxin - SPL UNCLASSIFIED SECTION Revised 12/11 Rx Only DESCRIPTION: Digoxin Tablets, USP are one of the cardiac (or digitalis) glycosides, a closely related group of drugs having in common specific effects on the myocardium. These drugs are found in a number of plants. Digoxin is extracted from the leaves of Digitalis lanata. The term “digitalis” is used to designate the whole group of...
• Dihydrocodeinon
• Dilaphylline Drops
• Dilaphylline Injections
• Dolopyrine
• Dolotramin
• Dolotramine
• Duremesan Suppositories
• Duremesan Tablets
• Elixir Tonique N
• Elpradil
• Elpradil HCT
• Emedrin N
• Ephedrin
• Epilantine
• Ergotonin
• Ergotonine
• Escalgin sans Codeine
• Escamox
• Escodaron
• Escodarone
• Escoflex
• Escoflex Compositum
• Escogripp
• Escogripp ohne Codein
• Escogripp sans Codeine
• Esconitro
• Escophylline
• Escoprim
• Escoprim Forte
• Escoretic
• Escoretic Forte
• Escoretic Mite
• Escothyol
• Escotussin
• Escozem
• Eucapinol
• Ferrascorbin Drops
• Ferrascorbin Tablets
• Finasterid
• Flavangin
• Fluoxetin
• Fordtran
• Fungex Ointment
• Fungex Powder
• Furocombin
• Furodermal
• Furodrix
• Gastracol
• Gastroprazol - 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...
• Gelparin
• Gelparine
• Glibenorm
• Glibenorme
• Glucocalcium
• Gluconormin
• Gluconormin Forte
• Gluconormin Mite
• Gluconormine
• Gluconormine Forte
• Gluconormine Mite
• Haemocortin Ointment
• Haemocortin Suppositories
• Haemolan Ointment
• Haemolan Suppositories
• Heparinol
• Histacyl Compositum
• Histacyl Cutane
• Histacylettes
• Histatec
• Hydrocodeinon
• Hydrocodon
• Hydrocortison - Pharmacological action Hydrocortison is a glucocorticosteroid. Hydrocortison 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...
• Hydrocortisone Comp
• Hydromorphoni Hydrochloridum
• Instacyl
• Jodoplex
• Kaliglutol
• Lidocain
• Lidocain-Epinephrin
• Lisinopril - WARNING: FETAL TOXICITY • When pregnancy is detected, discontinue lisinopril as soon as possible [see Warnings and Precautions (5.1) ]. • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see ...
• Lisinopril HCT
• Loperamid
• Losartan - Losartan is an angiotensin-receptor blocker (ARB) that may be used alone or with other agents to treat hypertension. Losartan and its longer acting metabolite, E-3174, lower blood pressure by antagonizing the renin-angiotensin-aldosterone system (RAAS); they compete with angiotensin II for binding to the type-1 angiotensin II receptor (AT1) subtype and prevents the blood pressure increasing effects of angiotensin II. Unlike angiotensin-converting enzyme (ACE) inhibitors, ARBs do not have the...
• Lubogliss
• Magenpulver Hafter
• Magentabletten Hafter
• Mefenacid
• Mefenacide
• Meprodil
• Meprodiol
• 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;...
• Methadon
• Mikutan N
• Morphini Hydrochloridum
• Morrhulan
• Neo-Hydro
• Neomycin; Hydrocortison
• Nifedicor - 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...
• Nifedicor Matrix - 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...
• Nifedicor Retard - Pharmacological action Nifedipine is aSelective calcium channel blocker class II, a derivative of dihydropyridine. This medication inhibits the entry of calcium into cardiomyocytes and vascular smooth muscle cells. Nifedipine has antianginal and hypotensive action. This drug lowers the tone of vascular smooth muscle. Nifedipine dilates coronary and peripheral arteries, lowers blood pressure and slightly - myocardial contractility, reduces afterload and myocardial oxygen demand. This...
• Nitroglycerin - SPL UNCLASSIFIED SECTION Rx DESCRIPTION: Molecular Structure Structural Formula SPL UNCLASSIFIED SECTION Molecular Structure ...
• Oestradiol
• Omeprazol - Pharmacological action Omeprazole is an inhibitor of H+ K+ ATPase. This medication inhibits the activity of H+-K+-ATPase in gastric parietal cells and thus blocks the final stage of hydrochloric acid secretion. This leads to a reduction in basal and stimulated secretion, regardless of the nature of the stimulus. Due to the reduction of acid secretion omeprazole reduces or normalizes the effects of acid in the esophagus in patients with reflux esophagitis. Omeprazole has a bactericidal...
• Oravil
• Ossofluor
• Otosan
• Pectramin
• Pepsi-Chlor
• Perfusion Mixte
• Pethidin
• Phenocillin
• Phlogantin
• Pommade Nasale Radix
• Pommade Nasale d'Apres Nager
• Pommade Nasale de Ruedi
• 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,...
• Prednisolon - Pharmacological action Prednisolone is a glucocorticosteroid (GCS). This medication inhibits the function of leukocytes and tissue macrophages. Prednisolone restricts the migration of leukocytes in the area of inflammation. This drug violates the ability of macrophages to phagocytosis and the formation of interleukin-1. Prednisolone contributes to the stabilization of lysosomal membranes, thereby reducing the concentration of proteolytic enzymes in inflammation. This medicine decreases...
• Prednisolon-P
• Prednison
• Primacton - 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...
• Primatenol - 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...
• Primatenol Plus
• Primofenac
• Primofenac Emulsions-Gel
• Principrox
• Progesteron
• Prontolax
• Prophyllen
• Radalgin
• Radix
• Radix Ointment
• Radix Poultice
• Rinosedin
• Risperidon - Risperidone information This medication works well for patients suffering from the agonies of bipolar diseases. Mostly, Risperidone helps individuals with schizophrenia and mania. By affecting the functions of different chemicals in the brain, this drug may provide relief to sufferers. However, before using this drug, patients need to be sure about the side effects that may occur. Risperidone can also be used for treating other disorders or as a complementary drug. Risperidone warnings ...
• Rudocain
• Rudocain Forte
• Rudocaine
• Rudocyclin
• Rudocycline
• Rudolac
• Rudopram
• Sedovalin Drops
• Sedovalin Tablets
• Septicol
• Septicortin
• Sertragen
• Simvast - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
• Simvastatin - Pharmacological action Simvastatin is a hypolipidemic agent from a group of statins, an inhibitor of HMG-CoA reductase. This medication is a prodrug because it has in its structure the closed lactone ring which is hydrolyzed after intake. Lipid-lowering effect of statins is associated with lower levels of total cholesterol by LDL-C. Reducing cholesterol is dose-dependent and is not linear but exponential. Statins do not affect the activity of lipoprotein and hepatic lipase, have no...
• Spasmo-Barbamin
• Spasmo-Barbamine
• Spasmo-Barbamine Compositum
• Spasmosol
• Spasmosol Drops
• Spasmosol Injections
• Sulfadiazin
• Tamsulosin - Tamsulosin is a selective antagonist at alpha-1A and alpha-1B-adrenoceptors in the prostate, prostatic capsule, prostatic urethra, and bladder neck. At least three discrete alpha1-adrenoceptor subtypes have been identified: alpha-1A, alpha-1B and alpha-1D; their distribution differs between human organs and tissue. Approximately 70% of the alpha1-receptors in human prostate are of the alpha-1A subtype. Blockage of these receptors causes relaxation of smooth muscles in the bladder neck and...
• Thermocutan
• Topaceta
• 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...
• Triplex - Pharmacological action Triplex is an antidepressant tricyclic group of compounds derived dibenzocycloheptadiene. The mechanism of antidepressant action is associated with an increased concentration of norepinephrine in the synapses and / or serotonin in the central nervous system depression due to reverse neuronal capture of these mediators. When anxiety and depressive states this medication reduces anxiety, agitation and depressive symptoms. Also this drug has some analgesic effect,...
• Triplex sans Codeine
• Tyrothricin
• Unathen
• Unathene
• Unatol
• Uriconorm - 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....
• Uriconorme - 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....
• Urodin - This medication is used to relieve symptoms caused by irritation of the urinary tract such as pain, burning, and the feeling of needing to urinate urgently or frequently. This drug does not treat the cause of the urinary irritation, but it can help relieve the symptoms while other treatments take effect. Phenazopyridine is a dye that works as a painkiller to soothe the lining of the urinary tract.
• Verapam
• Vita-Hexin
• Vitamin A - Retinol and derivatives of retinol that play an essential role in metabolic functioning of the retina, the growth of and differentiation of epithelial tissue, the growth of bone, reproduction, and the immune response. Dietary vitamin A is derived from a variety of carotenoids found in plants. It is enriched in the liver, egg yolks, and the fat component of dairy products. [PubChem] Indication: For the treatment of vitamin A deficiency. Vitamin A is effective for the treatment of Vitamin A...
• Vitamin C - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant. [PubChem] Indication: Used to treat vitamin C deficiency, scurvy, delayed wound and bone healing, urine acidification, and in general...
• Vitarubin
• Vitarubin Depot
• Vitarubin Superconc.
• 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