Unit Price:
৳ 150.00
(1 x 10: ৳ 1,500.00)
Strip Price:
৳ 1,500.00
Indications
Oseflu is indicated for prevention of flu (influenza) in adults and adolescents aged 13 years and over who have been in contact with someone diagnosed with flu; treatment of flu (influenza) in adults and in children over one year of age when the influenza virus is circulating in the community
Pharmacology
Oseltamivir is a prodrug of oseltamivir carboxylate. Oseltamivir carboxylate inhibits neuraminidase (sialidase), a viral surface enzyme which is responsible for the replication and infectivity of influenza virus A and B, thereby preventing the release of viruses from infected cells.
Dosage
Oseltamivir Phosphate may be taken with or without food. However, when taken with food, tolerability may be enhanced in some patients.
Standard oral dose for the treatment of influenza:
Standard oral dose for the treatment of influenza:
- Adults and Adolescents: The recommended oral dose of Oseltamivir for treatment of influenza in adults and adolescents 13 years and older is 75 mg twice daily for 5 days. Treatment should begin within 2 days of onset of symptoms of influenza.
- Pediatric patients: The safety and efficacy of Oseltamivir for prophylaxis of influenza in pediatric patients younger than 13 years of age have not been established.
- For prophylaxis of influenza in adults and adolescents 13 years and older following close contact with an infected individual: 75 mg once daily for at least 7 days. Therapy should begin within 2 days of exposure.
- For prophylaxis during a community outbreak of influenza: 75 mg once daily. Safety and efficacy have been demonstrated for up to 6 weeks. The duration of protection lasts for as long as dosing is continued.
Administration
May be taken with or without food. May be taken with meals to reduce GI discomfort. Cap may be opened & mixed with sweetened food products eg chocolate syr, sweetened condensed milk, apple sauce or yogurt. Swallow mixture immediately after preparation.
Interaction
Information derived from pharmacology and pharmacokinetic studies of Oseflu suggests that clinically significant drug interactions are unlikely. Co-administration with amoxicillin does not alter plasma levels of either compound.
Contraindications
Oseltamivir is contraindicated in patients with known hypersensitivity to any of the components of the product.
Side Effects
The most frequently reported adverse events are nausea and vomiting. These events generally of mild to moderate degree and usually are occurred on the first 2 days of administration. Additional adverse events occurring in <1% of patients receiving Oseflu for treatment include unstable angina, anemia, pseudomembranous colitis, humerus fracture, pneumonia, pyrexia, and peritonsillar abscess.
Pregnancy & Lactation
Pregnancy Category C: There are insufficient human data upon which to base an evaluation of risk of Oseltamivir Phosphate to the pregnant woman or developing fetus.
Nursing Mothers: It is not known whether oseltamivir or oseltamivir carboxylate is excreted in human milk. Oseltamivir Phosphate should, therefore, be used only if the potential benefit for the lactating mother justifies the potential risk to the breast-fed infant.
Nursing Mothers: It is not known whether oseltamivir or oseltamivir carboxylate is excreted in human milk. Oseltamivir Phosphate should, therefore, be used only if the potential benefit for the lactating mother justifies the potential risk to the breast-fed infant.
Precautions & Warnings
There is no evidence for efficacy of Oseflu Phosphate in any illness caused by agents other than influenza viruses Types A and B. Efficacy of Oseflu Phosphate in patients who begin treatment after 40 hours of symptoms has not been established.
Use in Special Populations
Hepatic Impairment: The safety and pharmacokinetics in patients with hepatic impairment have not been evaluated.
Renal Impairment: Dose adjustment is recommended for patients with a serum creatinine clearance <30 mL/min.
Geriatric Use: The safety of Oseflu Phosphate has been established in clinical studies.
Pediatric Use: The safety and efficacy of Oseflu Phosphate in pediatric patients younger than 1 year of age have not been studied. Oseflu Phosphate is not indicated for either treatment or prophylaxis of influenza in pediatric patients younger than 1 year of age.
Renal Impairment: Dose adjustment is recommended for patients with a serum creatinine clearance <30 mL/min.
Geriatric Use: The safety of Oseflu Phosphate has been established in clinical studies.
Pediatric Use: The safety and efficacy of Oseflu Phosphate in pediatric patients younger than 1 year of age have not been studied. Oseflu Phosphate is not indicated for either treatment or prophylaxis of influenza in pediatric patients younger than 1 year of age.
Overdose Effects
At present there has been no experience of over dose. Single dose of up to 1000 mg of Oseflu have been associated with nausea and/or vomiting.
Therapeutic Class
Respiratory viral infections (Influenza)
Storage Conditions
Store at 25°C. Reconstituted susp: Store between 2-8°C for up to 17 days or at 25°C for up to 10 days. Do not freeze.