Pharma company: admac pharma
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List of admac pharma products:
- Aclomax - 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...
- Adcal Syrup
- Adcal Tablets
- Adcip - Pharmacological action Adcip 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. Adcip is active against Staphylococcus spp. (including strains producing and not producing penicillinase,...
- Adcip-TZ
- Adclav
- Adcon - Pharmacological action Adcon 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 body....
- Adexim
- Adgat
- Admadol - Pharmacological action Admadol 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...
- Adnac-MR
- Adom-O
- Adpep-D
- Adpime
- Adprazole - Pharmacological action Adprazole 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. Adprazole has a bactericidal...
- Adprazole-D
- Advit
- Advit-DR
- Adzopip
- Afzone
- Afzone-S
- Alcored
- Alof - Pharmacological action Alof 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.,...
- Alof-T
- Alphacad
- Arthar
- Aspar
- Atenodip
- Atric Plus
- Atrovin
- Avicef
- Avicef-O
- Avicef-S
- Avikacin
- Azid - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Azid 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...
- Cad-Vital
- Cadec
- Cadgil
- Cadicin
- Cadifix - Cadifix information Cadifix is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Cadifix indications Cadifix 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. Cadifix may also be recommended...
- Cadiflam
- Cadiflam-NP
- Cadipip
- Cadizone
- Cadizone-S
- Cadizone-XP
- Cadmax - 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...
- Cadmentin
- Cadmoxin-CS
- Cadmoxin-LB
- Cadof - Pharmacological action Cadof 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.,...
- Cadol - Pharmacological action Cadol 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...
- Cadol-P
- Cadpime
- Cadpo-D
- Cadred
- Cadzid
- Caxyl
- Caxyl-P
- Cazita - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Cazita 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...
- Cefonex
- Cyfer
- Cyfer-P
- Decavillin
- Feric-Z
- Ferocid
- Fexim - Fexim information Fexim is a semi-synthetic cephalosporin antibiotic, destined for oral use, which is able to reduce the development of the drug resistant bacteria. Fexim indications Fexim 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. Fexim may also be recommended in the...
- Garamax
- Gatibenz
- Gaticad
- Irocid-Z
- K-Cip - Pharmacological action K-Cip 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. K-Cip is active against Staphylococcus spp. (including strains producing and not producing penicillinase,...
- K-Cip-TZ
- Kaxitel
- Kundo-V - Pharmacological action Kundo-V 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. Kundo-V 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 vaginalis. ...
- L-Cef
- Labdec
- Labicef-S
- Labzone
- Lazith - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Lazith 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...
- Lazopip
- Lebec-D
- Lebec-MR
- Lebec-NP
- Lebzone
- Leebec-NP
- Leecon - Pharmacological action Leecon 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 body....
- Leedol - Pharmacological action Leedol 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...
- Leedol-P
- Leemax - 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...
- Leemoxin-CS
- Leemoxin-LB
- Leepime
- Leetop
- Leetop-D
- Leeviz
- Lemicin
- Levobenz - Levobenz information Levobenz is type of drug that belongs to the group of medicines called antiepileptic drug. Levobenz indications This medication is indicated to control seizure. The precise way of how Levobenz works is not yet known. This medicine may also be used for purposes not mentioned here. Levobenz warnings This drug belongs in the FDA pregnancy category C. Levobenz may cause severe side effects to an unborn baby. Do not take Levobenz medication without consulting first...
- Levocad - Levocad information Levocad is type of drug that belongs to the group of medicines called antiepileptic drug. Levocad indications This medication is indicated to control seizure. The precise way of how Levocad works is not yet known. This medicine may also be used for purposes not mentioned here. Levocad warnings This drug belongs in the FDA pregnancy category C. Levocad may cause severe side effects to an unborn baby. Do not take Levocad medication without consulting first your...
- Lezone Injections
- Lezone Syrup
- Lezone-LB
- Lezone-S
- Lezone-XP
- Lin - Lin information Lin is type of drug that belongs to the group of medicines called antiepileptic drug. Lin indications This medication is indicated to control seizure. The precise way of how Lin works is not yet known. This medicine may also be used for purposes not mentioned here. Lin warnings This drug belongs in the FDA pregnancy category C. Lin may cause severe side effects to an unborn baby. Do not take Lin medication without consulting first your doctor if you are pregnant or...
- Loft - Pharmacological action Loft 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.,...
- Luroxime
- Maccef-LB
- Maccef-O
- Macliz
- Manzid
- Merenz
- Merocad
- Myzole - Pharmacological action Myzole 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 body....
- Pazole
- Pazole-D
- Peptazole
- Peptazole-D
- Rocal - Calcitriol is a man-made active form of vitamin D. Most people get enough vitamin D from exposure to the sun and from fortified food products (e.g., dairy products, vitamins). Vitamin D helps control parathyroid hormone and the levels of certain minerals (e.g., calcium , phosphorus) that are needed for building and keeping strong bones. Before regular vitamin D can be used by the body, it needs to be changed to the active form by the liver and kidneys . Calcitriol is used in patients with...
- Sea Vital
- Ziethem - Pharmacological action Azithromycin is a macrolide antibiotic of azalides group. Ziethem 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...
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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