Pharma company: international apex pharmaceuticals
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List of international apex pharmaceuticals products:
- Acutrex - Pharmacological action Acutrex 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...
- Aketon
- Anerobizol - Pharmacological action Anerobizol 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 Anerobizol is active against Helicobacter pylori. It is believed...
- Atracor
- Atropol
- Bactizef
- Bactrinol - Pharmacological action Bactrinol is a synthetic antimicrobial drug with broad spectrum bactericidal action. sulfamethoxazole has a bacteriostatic action, which is associated with inhibition of recycling process of PABA and a violation dihydrofolic acid's synthesis in bacterial cells. Trimethoprim inhibits the enzyme that is involved in the metabolism of folic acid converting dihydrofolate to tetrahydrofolate. Thus it is blocked two successive stages of the biosynthesis of purines and...
- Benaxil - Pharmacological action Benaxil is a blocker of histamine H1-receptors. It has antiallergic activity, has a local anesthetic, antispasmodic and mild ganglion blocking action. When Benaxil administered orally diphenhydramine has a sedative and hypnotic effects, has a moderate antiemetic effect and has a central holinoliticheskoy activity. When applied externally it has antiallergic effect. Pharmacokinetics Benaxil is rapidly absorbed from the gastrointestinal tract. Bioavailability is...
- Bricalin
- Broncoflem
- Cardiofast
- Cartine
- Ciprotal - Pharmacological action Ciprotal 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. Ciprotal is active against Staphylococcus spp. (including strains producing and not producing penicillinase,...
- Clarihist
- Clavimox
- Clomitene
- Dafenac - 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...
- Dalaclin
- Deme
- Dexticort - Pharmacological action Dexticort 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. Dexticort decreases capillary permeability caused by histamine release. This medicine inhibits the activity of fibroblasts and collagen formation. Dexticort inhibits the activity...
- Dobunex
- Dobutrim
- Dopamax
- Emlocaine
- Epicaine
- Floxol
- Fluxim
- Furide - 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...
- Garazin
- Gentaxin
- Hepaclex
- Heprin
- Heptin
- Hyzin - Hydroxyzine is used for the short-term treatment of nervousness and tension that may occur with certain mental/ mood disorders (e.g., anxiety , dementia ). It is also used to help manage withdrawal symptoms (e.g., anxiety, agitation) in alcoholics. Other uses include helping to decrease anxiety and nausea before/after surgery or during childbirth or helping certain narcotic pain relievers (e.g., meperidine ) work better. Hydroxyzine belongs to a class of medications called ...
- Inoflex - Pharmacological action Inoflex is an antimicrobial agents of broad-spectrum action type from fluoroquinolone group. Bactericidal action of ofloxacin is due to blockage of the enzyme DNA gyrase in bacterial cells. This medication is highly active against most of gram-negative bacteria: Escherichia coli, Salmonella spp., Shigella spp., Proteus spp., Morganella morganii, Klebsiella spp. (including Klebsiella pneumoniae), Enterobacter spp., Serratia spp., Citrobacter spp., Yersinia spp.,...
- Kanosole
- Kavocil
- Ketacor
- Klarid
- Klavic
- Klornik
- Kona-K
- Lanox
- Lanzole
- Levofin
- Levoflox - Levoflox information Levoflox is type of drug that belongs to the group of medicines called antiepileptic drug. Levoflox indications This medication is indicated to control seizure. The precise way of how Levoflox works is not yet known. This medicine may also be used for purposes not mentioned here. Levoflox warnings This drug belongs in the FDA pregnancy category C. Levoflox may cause severe side effects to an unborn baby. Do not take Levoflox medication without consulting first...
- Levoxin - 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...
- Lexiflox - Lexiflox information Lexiflox is type of drug that belongs to the group of medicines called antiepileptic drug. Lexiflox indications This medication is indicated to control seizure. The precise way of how Lexiflox works is not yet known. This medicine may also be used for purposes not mentioned here. Lexiflox warnings This drug belongs in the FDA pregnancy category C. Lexiflox may cause severe side effects to an unborn baby. Do not take Lexiflox medication without consulting first...
- Lomezek - Pharmacological action Lomezek 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. Lomezek has a bactericidal effect on...
- Loren
- Malarin
- Megacef
- Meropen - Meropenem is used to treat a wide variety of bacterial infections . This medication is known as a carbapenem-type antibiotic. It works by stopping the growth of bacteria.
- Merpurin
- Moriavit Capsules
- Morin
- Mozepam - Pharmacological action Mozepam 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. Mozepam increases the depth and duration of sleep. Sleep usually occurs in 20-40 minutes...
- Narlox
- Netilcin
- Netrozin
- Nobucaine - Pharmacological action Nobucaine is an antiarrhythmic agent of class IB, local anesthetic, a derivative of acetanilide. This medication has membrane stabilizing activity. Lidocaine causes a blockade of sodium channels of excitable membranes of neurons and the membrane of cardiomyocytes. This drug reduces the duration of the action potential and effective refractory period in Purkinje fibers, inhibits their automaticity. In this case, lidocaine inhibits electrical activity in depolarized,...
- Norphed
- Noruvec
- Nukaine
- Nyserin - Nyserin information Nyserin is a medicinal product used for the treatment and prevention of angina pectoris (a medical condition which occurs as the patients' coronary arteries become constricted, no longer allowing sufficient oxygen to reach the heart muscle). It is currently considered that Nitroglycerin allows the blood vessel walls to relax and dilate, thus increasing the oxygen flow to the cardiac muscles. Nyserin indications Nyserin may be employed as a prophylactic means only...
- Oflobay - Pharmacological action Oflobay 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. Oflobay is active against Staphylococcus spp. (including strains producing and not producing penicillinase,...
- Optamol
- Oxol
- Pamizep - Pharmacological action Pamizep is a benzodiazepine derivative tranquilizer. It provides anxiolytic, sedative, anticonvulsant, central muscle relaxant effect. The mechanism of action is associated with increased inhibitory effect of GABA in the CNS. Muscle relaxant effect is also due to the inhibition of spinal reflexes. This medication may cause anticholinergic effects. Pharmacokinetics Pamizep has rapid absorption. C max in plasma observed after 90 min. Plasma protein binding is 98%....
- Penam
- Pentazol
- Pentoxal
- Peptodin
- Phenerzin - Promethazine injection is used to treat nausea and vomiting related to certain conditions (e.g., after surgery, motion sickness). It is also used with other medication to treat life-threatening allergic symptoms ( anaphylaxis ) and reactions to blood products. The injectable form may be used to treat milder allergic reactions when you cannot take another medication by mouth. It may also be used before/after surgery, other procedures, or labor and delivery to help you feel calmer, to prevent...
- Phenerzine - Promethazine injection is used to treat nausea and vomiting related to certain conditions (e.g., after surgery, motion sickness). It is also used with other medication to treat life-threatening allergic symptoms ( anaphylaxis ) and reactions to blood products. The injectable form may be used to treat milder allergic reactions when you cannot take another medication by mouth. It may also be used before/after surgery, other procedures, or labor and delivery to help you feel calmer, to prevent...
- Polyzef
- Prosteride - Pharmacological action Prosteride is an inhibitor of 5-alpha reductase - an enzyme that converts testosterone into a more active dihydrotestosterone. Decreases the amount of dihydrotestosterone in the blood and prostate tissue. Inhibits the stimulatory effect of dihydrotestosterone on the development of prostate adenoma. Finasteride reduces the size of enlarged prostate, improves urine flow and reduce symptoms associated with benign prostatic hypertrophy. May be required several months of...
- Prostig
- Provestin
- Pyrinon
- Ropen
- Senpicaine
- Solodiab
- Solu-Ped
- Solucin
- Sublimax
- Syntox
- Tazobak
- Tikpid
- Trac
- Tracaine - Pharmacological action Tracaine 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 capture of noradrenaline activates the...
- Tral - Pharmacological action Tral is a NSAID, derivative of pyrrolizine-carboxylic acid. This medication has a marked analgesic effect, also has anti-inflammatory and mild antipyretic action. The mechanism of action is associated with inhibition of COX activity - the main enzyme metabolism of arachidonic acid, a precursor of prostaglandins, which play a major role in the pathogenesis of inflammation, pain and fever. Pharmacokinetics After oral administration Tral is absorbed from the...
- Valzepam - Pharmacological action Valzepam is a benzodiazepine derivative tranquilizer. It provides anxiolytic, sedative, anticonvulsant, central muscle relaxant effect. The mechanism of action is associated with increased inhibitory effect of GABA in the CNS. Muscle relaxant effect is also due to the inhibition of spinal reflexes. This medication may cause anticholinergic effects. Pharmacokinetics Valzepam has rapid absorption. C max in plasma observed after 90 min. Plasma protein binding is...
- Vancin
- Virtex
- Visol
- Xepacaine - Pharmacological action Xepacaine is an antiarrhythmic agent of class IB, local anesthetic, a derivative of acetanilide. This medication has membrane stabilizing activity. Lidocaine causes a blockade of sodium channels of excitable membranes of neurons and the membrane of cardiomyocytes. This drug reduces the duration of the action potential and effective refractory period in Purkinje fibers, inhibits their automaticity. In this case, lidocaine inhibits electrical activity in depolarized,...
- Zantol - Pharmacological action Zantol 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...
- Zeclor
- Zepax
- Zepotex
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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