Eluphor, 200 mg/5 ml suspension 90 ml
€13.96 €12.22
It is assumed that antimicrobial activity of nifuroxazide is caused by the presence of NO2-group in its composition, which causes inhibition of dehydrogenase activity and disrupts protein synthesis in pathogenic bacteria.
Active against Gram-positive microorganisms (Streptococcus aureus, Staphylococcus pyogenes, Clostridium), Gram-negative enterobacteriaceae (Escherihia coli, Salmonella spp, Shigella spp., Klebsiella spp., Enterobacter spp., Vibrio cholerae, Campylobacter jejuni, Edwarsiella, Citrobacter, Yersinia enterocolitica). In acute bacterial diarrhea it restores intestinal eubiosis. In case of infection with enterotropic viruses it prevents the development of bacterial superinfection.
Pharmacokinetics
After oral administration nifuroxazide is practically not absorbed from the digestive tract and its antibacterial effect is exclusively in the intestinal lumen. It is completely eliminated through the gastrointestinal tract. The elimination rate depends both on the dose of the drug and on the motility of the intestinal tract.
Indications
Active ingredient
Composition
How to take, the dosage
It is administered orally.
For dosing use a dosage spoon of 5 ml with graduation of 2.5 ml.
The suspension should be shaken well before use.
Children 1-6 months: 2.5 ml 2-3 times a day (at intervals of 8 to 12 hours).
Children from 7 months to 2 years of age: 2.5 ml 4 times a day (at 8-hour intervals).
Children from 3 to 7 years of age: 5 ml 3 times a day (at 8-hour intervals).
Children over 7 years of age and adults: 5 ml 3-4 times a day (at 6-8-hour intervals). Therapy with nifuroxazide should not last more than 7 days.
Special Instructions
In treatment of diarrhea simultaneously with therapy with nifuroxazide rehydration therapy (oral or intravenous) should be conducted in accordance with the patient’s condition and intensity of diarrhea.
Alcohol use during therapy with nifuroxazide is prohibited.
Before administration of suspension in infants should be excluded their congenital deficiency of sucrose digesting enzymes.
The drug does not affect psychomotor performance and ability to drive and operate machinery.
Contraindications
Side effects
Overdose
Similarities
Weight | 0.137 kg |
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Shelf life | 3 years Do not use after the expiration date. |
Conditions of storage | At 15 ° to 30 ° C. Keep out of reach of children. Opened bottle should be stored for no more than 7 days. |
Manufacturer | Ozon, Russia |
Medication form | oral suspension |
Brand | Ozon |
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