Pharma company: biomax biotechnics
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List of biomax biotechnics products:
- Amalset
- Baclin
- Bacmax - Pharmacological action Bacmax 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 ...
- Bio-10
- Bio-AZ - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Bio-AZ 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...
- Borox
- Borox-L
- Carbosyl Capsules
- Carbosyl Syrup
- Chocy
- Civir - Pharmacological action Civir 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 Herpes...
- Clavogard
- Clavogard-Kid
- Cogof
- Cogof-A
- Colep
- Cortygard - Pharmacological action Cortygard is a glucocorticosteroid. Cortygard 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...
- Corus
- Corus-FA
- Depomax
- Depomax-S
- Dicimax-G
- Diplom
- Dotacid
- Ezemax-A
- FS - Pharmacological action FS 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 descending...
- FS Plus
- FS-D
- Flamace-MR
- Flamace-P
- Flamace-SP
- Furomax
- Glisu
- IMM-4
- Inogat-O
- Ixidol
- Kampi
- Lofy - 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...
- Lutacare - Pharmacological action Lutacare is a progestogen. This medication causes a transition in the endometrium of proliferative phase, called follicular hormone in the secretory phase, and after fertilization promotes its transition to a state necessary for the development of a fertilized egg. Progesterone reduces the excitability and contractility of the muscles of the uterus and fallopian tubes, stimulates the development of terminal elements of the breast. It has no androgenic activity. This...
- Megapril - Megapril information Megapril belongs to the class of drugs classified as ACE inhibitors or Angiotensin-Converting-Enzyme inhibitor. Megapril indications This product is a drug prescribed for the treatment of hypertension or high blood pressure, and for the prevention of heart failures succeeding heart attacks. Megapril is also used for the prevention of heart attacks, stroke and other heart related problems. Megapril warnings The medication is major allergen especially to patients...
- Methicap
- NMX
- Napi-D
- Oflagard - Pharmacological action Oflagard 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.,...
- Oflagard-O
- Oflagard-OL
- Omore - Pharmacological action Omore 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. Omore has a bactericidal effect on...
- Omore-D
- Ortocal-CT
- Osul-S
- Ovitec
- Pave - This medication is used to increase blood flow throughout the body, including the heart and the brain . Papaverine is a vasodilator. It works by relaxing the muscles in the blood vessels. Papaverine is also an antiarrhythmic medication that treats certain abnormal heartbeats (ventricular arrhythmias). It works by blocking the abnormal electrical activity in the heart so a normal heart beat can return. It may also help the heart beat better by increasing the blood flow to the heart.
- Pave-D
- Pave-DSR
- Pozol
- Preneu - Pharmacological action Preneu is an antiepileptic drugs which active ingredient is an analogue of gamma-aminobutyric acid (GABA). Although the exact mechanism of action of pregabalin still uncertain, it was found that pregabalin binds with an additional subunit (alpha-2-delta protein) of voltage-dependent calcium channels in the CNS, it is assumed that such binding may contribute to the manifestation of its analgesic and anticonvulsant effects. Pharmacokinetics Pharmacokinetics of...
- Preneu-M
- Pynor-DT
- Pythene
- Raver
- Raver-D
- Raver-DSR
- Raver-IT
- Relor Forte
- Rescucef
- Rescucef-T
- Riflo
- Romax
- Sider-K
- Sider-P
- Sologab - Pharmacological action Sologab 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...
- Sologab-M
- Sologard
- Sologard-S
- Sologard-T
- Thelexin
- Tot
- Urlo - Pharmacological action Urlo 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. Allopurinol increases...
- Vator - Pharmacological action Vator 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 not...
- Vator-F
- Vee
- Vee-C
- Verto
- Verto-C - Pharmacological action Verto-C 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. Verto-C 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 excitability...
- Vertohist
- Vertomin
- Vologard - Vologard information Vologard is type of drug that belongs to the group of medicines called antiepileptic drug. Vologard indications This medication is indicated to control seizure. The precise way of how Vologard works is not yet known. This medicine may also be used for purposes not mentioned here. Vologard warnings This drug belongs in the FDA pregnancy category C. Vologard may cause severe side effects to an unborn baby. Do not take Vologard medication without consulting first...
- Vomclor
- Vomna-F
- Xefotil
- Xenater
- Xenater-MD
- Xirom - Pharmacological action Xirom 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 Xirom used externally it weakens or suppresses inflammation and joint pain at rest and in...
- Xoc
- Zaxid
- Zebose
- Zitmik
- Zofu-ER
- Zolar-P
- Zolimax
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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