Tamiflu (Oseltamivir) Dosage
For adults and adolescents ≥13 years, the standard treatment dose is 75 mg orally twice daily for 5 days, and for prophylaxis, 75 mg once daily for at least 10 days. 1, 2, 3
Treatment Dosing (5 Days Duration)
Adults and Adolescents (≥13 years)
- 75 mg orally twice daily for 5 days 1, 2, 3
- Must be initiated within 48 hours of symptom onset for maximum effectiveness 1, 2
- Can be taken with or without food, though taking with meals improves gastrointestinal tolerability 1, 2
Pediatric Patients (≥12 months to 12 years) - Weight-Based Dosing
- ≤15 kg (≤33 lb): 30 mg twice daily 1, 2, 3
- >15-23 kg (>33-51 lb): 45 mg twice daily 1, 2, 3
- >23-40 kg (>51-88 lb): 60 mg twice daily 1, 2, 3
- >40 kg (>88 lb): 75 mg twice daily 1, 2, 3
Infants (<12 months)
- 9-11 months: 3.5 mg/kg per dose twice daily 1, 2
- Term infants 0-8 months: 3 mg/kg per dose twice daily 1, 2, 3
Preterm Infants (Postmenstrual Age-Based)
- <38 weeks postmenstrual age: 1.0 mg/kg twice daily 1, 2
- 38-40 weeks postmenstrual age: 1.5 mg/kg twice daily 1, 2
- >40 weeks postmenstrual age: 3.0 mg/kg twice daily 1, 2
Prophylaxis Dosing
Adults and Adolescents (≥13 years)
- 75 mg orally once daily 1, 3
- Duration: 10 days for post-exposure prophylaxis 1, 3
- Duration: Up to 6 weeks for seasonal/community outbreak prophylaxis 1, 3
- Duration: Up to 12 weeks in immunocompromised patients 1, 3
- Must be initiated within 48 hours following close contact with an infected individual 1
Pediatric Patients (1-12 years) - Weight-Based Dosing
- ≤15 kg: 30 mg once daily 1, 3
- >15-23 kg: 45 mg once daily 1, 3
- >23-40 kg: 60 mg once daily 1, 3
- >40 kg: 75 mg once daily 1, 3
- Duration: 10 days post-exposure or up to 6 weeks for community outbreak 1, 3
Infants (3-11 months)
- 3 mg/kg once daily for 10 days 1
- Prophylaxis is not recommended for infants <3 months unless the situation is judged critical due to limited safety data 1
Renal Impairment Adjustments
For patients with creatinine clearance 10-30 mL/min, dose reduction is essential to avoid toxicity: 1, 2, 3
Treatment Dosing
Prophylaxis Dosing
Formulations and Administration
Available Forms
Oral Suspension Dosing Volumes
Administration Tips
- Capsules can be opened and contents mixed with liquid for patients who cannot swallow capsules whole 1
- If commercial oral suspension is unavailable, pharmacies can compound a suspension using capsule contents mixed with simple syrup or Ora-Sweet SF to achieve 6 mg/mL concentration 1
- For infants <1 year, use an appropriate dosing device that can accurately measure small volumes 3
Critical Clinical Considerations
Timing
Treatment must be initiated within 48 hours of symptom onset for maximum benefit - this reduces illness duration by 29-35 hours (25-30% reduction) compared to placebo 1, 4. Earlier initiation within 24 hours provides even greater benefit, reducing symptoms by 37-40% 4.
Common Adverse Effects
- Nausea and vomiting occur in approximately 5-15% of patients (compared to 8% on placebo) 1
- Gastrointestinal effects are mild, transient, and significantly reduced when taken with food 1, 5
- Headache and skin reactions may also occur 1
Drug Interactions
Avoid live attenuated influenza vaccine (LAIV) within 48 hours before oseltamivir use, and do not use oseltamivir for 14 days after LAIV vaccination 1