Indications |
Oral Influenza A and B Adult: 75 mg bid for 5 days. Initiate treatment within 2 days of onset of symptoms. Child: 1-12 yr: Wt ≤15 kg: 30 mg bid; >15-23 kg: 45 mg bid; >23-40 kg: 60 mg bid; >40 kg: 75 mg bid. Initiate treatment within 2 days of onset of symptoms. Duration of treatment: 5 days. Renal impairment: Dialysis: Not recommended.
Oral Prophylaxis of influenza A and B Adult: 75 mg once daily for 10 days. Initiate treatment within 2 days of exposure. For community outbreak: May continue dosing for up to 6 wk. Child: 1-12 yr: Wt ≤15 kg: 30 mg once daily; >15-23 kg: 45 mg once daily; >23-40 kg: 60 mg once daily; >40 kg: 75 mg once daily. Initiate treatment within 2 days of contact with an infected individual. Duration of treatment: 10 days. Renal impairment: Dialysis: Not recommended.
Special Populations: Renal impairment: CrCl 10-30 mL/min: Treatment: 75 mg once a day for 5 days. Prophylaxis: 75 mg every other day. Creatinine clearance <10 mL/min: No recommended dosage adjustment. Hepatic impairment: No recommended dosage adjustment. Reconstitution: Oral suspension: Reconstitute with 23 ml water to make 25 ml suspension. |
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Contraindications |
Hypersensitivity. Severe renal impairment. | ||||||||||||
Warnings / Precautions |
Moderate renal impairment. Pregnancy and lactation. Chronic cardiac disease, hepatic impairment, respiratory disease, immunocompromised patients. | ||||||||||||
Adverse Reactions |
Nausea, vomiting, abdominal pain, bronchitis, insomnia, vertigo, diarrhoea, dizziness, headache, cough, fatigue, unstable angina, anaemia, pseudomembranous colitis, pneumonia, pyrexia, peritonsillar abscess, elevated liver enzymes, hepatitis, aches and pains, dyspepsia, rhinorrhoea, upper respiratory-tract infections. In children: Vomiting, other GI disturbances, asthma, bronchitis, conjunctivitis, dermatitis, epistaxis, ear disorders, otitis media, lymphadenopathy, pneumonia, sinusitis. Potentially Fatal: Anaphylaxis, severe dermatologic reactions. |
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Overdose Reactions |
Symptoms include nausea and vomiting. | ||||||||||||
Mechanism of Actions |
Oseltamivir is a prodrug of oseltamivir carboxylate (OC). OC is a potent selective competitive inhibitor of neuraminidase (an enzyme required for viral replication) of the influenza virus A and B. It prevents the release of viruses from infected host cell. Absorption: Readily absorbed from the GI tract (oral). Distribution: Protein-binding: 3% (carboxylate); 42% (parent drug). Metabolism: Hepatic; extensively metabolised to oseltamivir carboxylate. Excretion: Via urine. Half-life: 1-3 hr. |
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Administration |
May be taken with or without food. (May be taken w/ meals to reduce GI discomfort. Cap may be opened & mixed w/ sweetened food products eg chocolate syr, sweetened condensed milk, apple sauce or yogurt. Swallow mixture immediately after preparation.) |
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Storage Conditions |
Oral: Capsule: Store at 25°C (77°F). Oral suspension: Store at 25°C (77°F). Once reconstituted, refrigerate at 2-8°C (36-46°F). Do not freeze and use within 10 days. | ||||||||||||
ATC Classification |
J05AH02 - oseltamivir ; Belongs to the class of neuraminidase inhibitors. Used in the systemic treatment of viral infections. | ||||||||||||
Storage |
Oral: Capsule: Store at 25°C (77°F). Oral suspension: Store at 25°C (77°F). Once reconstituted, refrigerate at 2-8°C (36-46°F). Do not freeze and use within 10 days. | ||||||||||||
Available As |
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Oseltamivir
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Oseltamivir Containing Brands
Oseltamivir is used in following diseases
Drug - Drug Interactions of Oseltamivir
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