Tamiflu (Oseltamivir) Dosing Recommendations
For adults and adolescents ≥13 years, the standard treatment dose is 75 mg orally twice daily for 5 days, and prophylaxis is 75 mg once daily for 10 days, with mandatory dose reductions required for renal impairment (creatinine clearance <60 mL/min). 1, 2, 3
Adult and Adolescent Dosing (≥13 years)
Treatment regimen:
- 75 mg orally twice daily for 5 days 1, 2, 3
- Should be initiated within 48 hours of symptom onset for maximum benefit, though treatment beyond 48 hours still provides substantial mortality reduction in hospitalized patients 4, 5
- Can be taken with or without food, though administration with meals improves gastrointestinal tolerability 1, 2, 6
Prophylaxis regimen:
- 75 mg once daily for 10 days (post-exposure prophylaxis) 1, 2, 6
- 75 mg once daily for up to 6 weeks during community outbreaks 1, 3
- Should be initiated within 48 hours of exposure to infected individuals 4, 6
Pediatric Dosing (≥1 year)
Weight-based dosing is preferred for children 1-12 years: 1, 2
Treatment (twice daily for 5 days):
Prophylaxis (once daily for 10 days):
Infant Dosing (<1 year)
Term infants (≥2 weeks to <1 year):
- 9-11 months: 3.5 mg/kg per dose twice daily for treatment 1, 2, 4
- 0-8 months: 3 mg/kg per dose twice daily for treatment 1, 2, 4
- 3-11 months: 3 mg/kg once daily for prophylaxis 1, 2, 6
- Prophylaxis is not recommended for infants <3 months unless the situation is judged critical due to limited safety data 1, 6
Preterm infants require substantially lower doses based on postmenstrual age (gestational age + chronological age): 1, 2
- <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
The lower dosing for preterm infants is critical because immature renal function leads to slower drug clearance and risk of toxic drug accumulation if term infant doses are used 1
Renal Impairment Dosing Adjustments
Dose adjustments are mandatory when creatinine clearance falls below 60 mL/min: 2, 6
Creatinine clearance 10-30 mL/min:
- Treatment: 75 mg once daily (instead of twice daily) for 5 days 1, 3
- Prophylaxis: 30 mg once daily for 10 days OR 75 mg every other day for 10 days (5 total doses) 1, 3
End-stage renal disease (ESRD) on hemodialysis:
- Treatment: 30 mg immediately, then 30 mg after every hemodialysis cycle (not to exceed 5 days) 3
- Prophylaxis: 30 mg immediately, then 30 mg after alternate hemodialysis cycles for recommended duration 3
ESRD on continuous ambulatory peritoneal dialysis (CAPD):
- Treatment: Single 30 mg dose immediately 3
- Prophylaxis: 30 mg immediately, then 30 mg once weekly for recommended duration 3
Oseltamivir is not recommended for ESRD patients not undergoing dialysis 3
Formulation and Administration
Available formulations: 1, 2, 3
- Capsules: 30 mg, 45 mg, 75 mg
- Oral suspension: 6 mg/mL (when reconstituted from powder)
Oral suspension dosing volumes (6 mg/mL concentration): 1, 2
- 30 mg dose = 5 mL
- 45 mg dose = 7.5 mL
- 60 mg dose = 10 mL
- 75 mg dose = 12.5 mL
If commercial suspension is unavailable, pharmacies can compound a suspension (6 mg/mL concentration) based on package insert instructions 1, 2
Special Populations
Pregnancy:
- Pregnant women receive the same dosing as non-pregnant adults: 75 mg twice daily for 5 days 4
- Pregnancy substantially increases risk of severe influenza complications, and the benefit-risk profile strongly favors treatment 4
- Breastfeeding is not a contraindication to oseltamivir use 4, 6
Elderly patients (≥65 years):
- Standard adult dosing (75 mg twice daily) applies if renal function is normal 6
- The critical consideration is renal function, not age—dose reductions are mandatory when creatinine clearance falls below 60 mL/min 6
High-risk patients (chronic cardiac/respiratory disease, diabetes, immunocompromised):
- Use standard age/weight-based dosing 1, 4, 6
- Treatment should not be delayed while awaiting laboratory confirmation 4, 6
- Immunocompromised patients may require extended treatment duration beyond 5 days if illness is prolonged 4
Critical Timing Considerations
Treatment initiation:
- Maximum benefit occurs when started within 48 hours of symptom onset, reducing illness duration by 1-1.5 days 4, 6, 7
- Do not withhold treatment in hospitalized or high-risk patients presenting beyond 48 hours, as significant mortality reduction still occurs 4, 8, 5
- Recent evidence demonstrates an 82% reduction in odds of in-patient death with standard oseltamivir treatment in PCR-confirmed influenza 5
Prophylaxis initiation:
Common Pitfalls and Caveats
Avoid these errors:
- Do not use term infant dosing (3 mg/kg) for preterm infants—this leads to toxic drug concentrations due to immature renal function 1
- Do not confuse GFR with creatinine clearance when calculating renal dosing adjustments 2
- Do not withhold treatment due to mild illness or fever alone—these are not contraindications 6
- Avoid live attenuated influenza vaccine (LAIV) within 48 hours before oseltamivir or for 14 days after oseltamivir use 4, 6, 3
Gastrointestinal tolerability:
- Nausea and vomiting occur in approximately 10-15% of patients 2, 6
- Taking oseltamivir with food significantly reduces gastrointestinal side effects 1, 2, 6
- These effects are typically mild, transient, and rarely lead to discontinuation 7, 9
Resistance considerations: