Pharma company: degort's chemical
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List of degort's chemical products:
- Albatrina
- Ameblin - Pharmacological action Ameblin 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 Ameblin is active against Helicobacter pylori. It is believed that...
- Anfloxin
- Artriden
- Azogen
- Azpencil - Pharmacological action Ampicillin is an antibiotic of semisynthetic broad-spectrum penicillin group. This medication has a bactericidal effect by suppressing the synthesis of bacterial cell walls. Ampicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (with the exception of strains producing penicillinase), Streptococcus spp., Enterococcus spp., Listeria monocytogenes; aerobic gram-negative bacteria: Neisseria gonorrhoeae, Neisseria meningitidis, Escherichia coli,...
- Aztrolen
- Bariclor
- Barigesic
- Biofilen - 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...
- Bradelmin
- Bramin
- Bronar
- CK-2
- Celfax
- Convifer con Hierro
- Croferron
- Cronavit
- Crovalen
- Dartrizon
- Deamcilina - Pharmacological action Ampicillin is an antibiotic of semisynthetic broad-spectrum penicillin group. This medication has a bactericidal effect by suppressing the synthesis of bacterial cell walls. Ampicillin is active against aerobic gram-positive bacteria: Staphylococcus spp. (with the exception of strains producing penicillinase), Streptococcus spp., Enterococcus spp., Listeria monocytogenes; aerobic gram-negative bacteria: Neisseria gonorrhoeae, Neisseria meningitidis, Escherichia coli,...
- Debequin - Pharmacological action Dextromethorphan is an antitussive medication. Inhibiting the excitability of the cough center this medicine suppresses the cough of any origin. Dextromethorphan has not addiction effects and it has no analgesic and hypnotic action. Dextromethorphan starts to act after 10-30 minutes after oral administration, the duration of therapeutic action: 5-6 hours for adults and 6-9 hours for children. Dextromethorphan is an optical isomer of levomethorphan which is similar to...
- Debequin-C
- Degortkap
- Dequin
- Dertrifort - 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....
- Diazolen - Pharmacological action Mebendazole is a worming medication a broad spectrum of action, it is most effective when enterobioze. This drug causes irreversible disturbance of glucose utilization in the body of the worm and inhibits the synthesis of ATP. Pharmacokinetics Mebendazole is practically not absorbed from the gastrointestinal tract. The plasma protein binding is 90%. This medication is distributed unevenly in organs and accumulates in adipose tissue, liver, and larvae of helminths...
- Dicentril
- Dolfort-DE
- Dualizol - Pharmacological action Metronidazole 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 Metronidazole is active against Helicobacter pylori. It is...
- Duciclon
- Duplat
- Ebromin-P
- Emipastin
- Espabion
- Espraden
- Estuvina
- Evadol
- Exafil
- Ferro-Terapina
- Floxantina
- Flucol
- Fluvicil
- Fravit
- Friobax
- Gastrodina
- Glandicin - Pharmacological action Piroxicam 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 Piroxicam used externally it weakens or suppresses inflammation and joint pain at rest...
- Glipar
- Hidroxovit
- Ibacnol - Pharmacological action Ofloxacin 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.,...
- Indozul
- Inprax
- Lergosin - 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...
- Lergosin A
- Lisibac
- Midolen
- Neo-Kap
- Neokap
- Oblant - 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...
- Octex
- Octiban
- Osemin - 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...
- Palatrin
- Prenalon
- Proxalin - Naproxen information Naproxen is an anti-inflammatory non-steroidal anti-inflammatory (NSAID) medicine. Naproxen Pascual Laboratories's actions help reduce the chemicals found in the patient's organism that are usually responsible for the triggering of inflammation and pain. Naproxen indications Naproxen is a drug normally prescribed in the treatment of pain, stiffness or inflammation that are usually triggered by medical disorders such as Gout, Osteoarthritis, menstruation abdominal...
- Proxalin Plus
- Reductel
- Remisol
- Remisol-Pls
- Remisol-Plus
- Sediclon
- Seredyn
- Suprin
- Suronit
- Terodul
- Traplicina
- Triseptil
- Vermicol - Pharmacological action Mebendazole is a worming medication a broad spectrum of action, it is most effective when enterobioze. This drug causes irreversible disturbance of glucose utilization in the body of the worm and inhibits the synthesis of ATP. Pharmacokinetics Mebendazole is practically not absorbed from the gastrointestinal tract. The plasma protein binding is 90%. This medication is distributed unevenly in organs and accumulates in adipose tissue, liver, and larvae of helminths...
- Vi-Dea-C
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The information was verified by Dr. Rachana Salvi, MD Pharmacology
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