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DRUGS & SUPPLEMENTS
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Pharma company: alna biotech
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List of alna biotech products:
- Alcyp-T
- Aleflox - Aleflox information Aleflox is type of drug that belongs to the group of medicines called antiepileptic drug. Aleflox indications This medication is indicated to control seizure. The precise way of how Aleflox works is not yet known. This medicine may also be used for purposes not mentioned here. Aleflox warnings This drug belongs in the FDA pregnancy category C. Aleflox may cause severe side effects to an unborn baby. Do not take Aleflox medication without consulting first your...
- Alna-ORS
- Alnabate
- Alnacef
- Alnacef-S
- Alnacef-T
- Alnacer
- Alnacer Cold
- Alnacet
- Alnacet-AL
- Alnacet-M
- Alnacet-M Kid
- Alnaclox
- Alnaclox-Kid
- Alnaclox-LB
- Alnaclox-LB Kid
- Alnacob-G
- Alnacob-P
- Alnacort
- Alnadine
- Alnaferon Syrup
- Alnaferon Tablets
- Alnagest - Pharmacological action Alnagest 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...
- Alnamax-G
- Alnamax-GM
- Alnamet-G
- Alnamet-GP
- Alnamet-GSR
- Alnamet-SR
- Alnamox - Pharmacological action Alnamox 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...
- Alnamycin
- Alnaparin
- Alnaprazol
- Alnase
- Alnase Gel
- Alnase-MR
- Alnase-P
- Alnase-SP
- Alnathrin
- Alnavas - Pharmacological action Alnavas 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...
- Alnavas-EZ
- Alnavas-F
- Alnavit Capsules
- Alnavit Drops
- Alnavit Syrup
- Alur - Pharmacological action Alur 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...
- Alvi
- At-Last
- Baclodol - Pharmacological action Baclodol 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 ...
- Beta-Mep
- Calpime
- Cefumep-S
- Cefupop - Cefupop information Cefupop is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Cefupop indications Cefupop is usually prescribed by doctors and personal health care providers to patients who are suffering from bacterial infections of the ears, throat, chest, urinary tract and to the individuals who have been diagnosed with the presence of a mild form of gonorrhea. Cefupop may also be recommended...
- Cefupop-CV
- Cefupop-XL
- Cipromep - Pharmacological action Cipromep 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. Cipromep is active against Staphylococcus spp. (including strains producing and not producing penicillinase,...
- Cobimep-G
- Cobimep-P
- Cofal
- Cofal-D
- Cofev
- Cofev-P
- Copod
- Copod-B
- Didol - Pharmacological action Didol 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...
- Didol-D
- Didol-P
- Dimyclox
- Dru - 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...
- Dru-MR
- Dru-S
- Drucort - Pharmacological action Drucort is a glucocorticosteroid. Drucort 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...
- Dudot
- Dudot-M
- Edrucef
- Edrucef-CV
- Feofer
- Fesu
- Fesu-XT
- Flukamep - Pharmacological action Flukamep 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...
- Gludel
- Hartivit
- Hyss - Pharmacological action Hyss is a glucocorticosteroid. Hyss 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...
- ITN
- Iceron
- Irovista
- Itha - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Itha 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...
- Jivak
- Kefbactam
- Kefbactam Forte
- Lamna-C
- Lemna-C
- Lemna-C Kid
- Logcef - Logcef information Logcef is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Logcef indications Logcef is usually prescribed by doctors and personal health care providers to patients who are suffering from bacterial infections of the ears, throat, chest, urinary tract and to the individuals who have been diagnosed with the presence of a mild form of gonorrhea. Logcef may also be recommended in...
- Logcef-CV
- Logflox - Pharmacological action Logflox 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.,...
- Logflox-OZ
- Logpod
- Lok-H
- Lysoplex
- Meffnex
- Mep-Fluron
- Mep-Fovea
- Mep-Orva - Pharmacological action Mep-Orva 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.,...
- Mepcef
- Mepcin
- Mepef-S
- Meptrop
- Meptrop-P
- Mepycep
- Mepyvit-CT
- Meris
- Meris-D
- Midol - Pharmacological action Midol 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...
- Mistra
- Moira
- Monal
- Moxafav
- Moxi-Mep-D
- Mudot
- Natam
- Neobate
- Nimumep
- Novee-Q Syrup
- Novee-Q Tablets
- Nuradef
- Ondrovit
- Ondrovit-MD
- Oxyla-AL
- Pantamep
- Pantamep-DSR
- Papcef
- Papcef-CV
- Pirozy - Pharmacological action Pirozy 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 Pirozy used externally it weakens or suppresses inflammation and joint pain at rest and in...
- Proalna Capsules
- Proalna Powder
- Proten
- Provo - Pharmacological action Provo 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.,...
- Provo-NX
- Provo-OZ
- Rabemep
- Rauf
- Rauf-E
- Resmep
- Rhineedclear-S - Pharmacological action Ions of sodium and chlorine are the major inorganic components of the extracellular fluid, maintaining an appropriate osmotic pressure of blood plasma and extracellular fluid. Isotonic solution of Rhineedclear-S fills a deficit of body fluids during dehydration. Hypertonic solution of sodium chloride for IV injection provides a correction of osmotic pressure of extracellular fluid and blood plasma. When applied topically in ophthalmology sodium chloride has...
- Rhinoclear Drops
- Rhinoclear Tablets
- Rhinoclear-P
- Rive
- Rive-D
- Rive-DSR
- Rive-IT
- S-Bil
- Sahcef
- Sahcef-T
- Sapsyl Capsules
- Sapsyl Syrup
- Sapsyl-XT
- Sedacam-P
- Seral-D
- Sinucal Syrup
- Sinucal Tablets
- Sinucal-CT
- Solopan
- Solopan-D
- Solopan-DSR
- Sucan
- Sucan-O
- Suctum-CF
- Tamonac-P
- Tamonac-SP
- Thou Capsules
- Thou Syrup
- Toraflam
- Toraflam-P
- Toraflam-T
- Tra-MF
- Tript
- Uriflax
- Vakfresh - Pharmacological action Vakfresh is an antiseptic agent. chlorhexidine is active against vegetative forms of gram-negative and gram-positive bacteria and yeasts, dermatophytes and lipophilic viruses. This medicine has effect for bacterial spores only at elevated temperatures. It cleans and disinfects the skin without causing damage. Why is Vakfresh prescribed? For local use of Vakfresh: trichomonas coleitis, cervical erosion, itching of the vulva, prevention of sexually transmitted...
- Vakgum
- Valimep-CR
- Vanmax
- Vixinate
- Vocin - Vocin information Vocin is type of drug that belongs to the group of medicines called antiepileptic drug. Vocin indications This medication is indicated to control seizure. The precise way of how Vocin works is not yet known. This medicine may also be used for purposes not mentioned here. Vocin warnings This drug belongs in the FDA pregnancy category C. Vocin may cause severe side effects to an unborn baby. Do not take Vocin medication without consulting first your doctor if you...
- Vucil
- Vucillin
- X-Pro
- X-Pro-SF
- Yomzole - Pharmacological action Yomzole 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. Yomzole has a bactericidal effect on...
- Yomzole-D
- Zicor - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Zicor 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...
- Zivert - Pharmacological action Zivert 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. Zivert 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...
- Zivert-D
- Zivocet
- Zivocet-Al
- Zivocet-M
- Zynar
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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