Oseltamivir Dosing Recommendations
For adults and adolescents ≥13 years, administer oseltamivir 75 mg orally twice daily for 5 days for treatment, or 75 mg once daily for prophylaxis, with dose reductions required for moderate-to-severe renal impairment (creatinine clearance 10-30 mL/min to 75 mg once daily for treatment or 30 mg once daily for prophylaxis). 1, 2, 3
Adult and Adolescent Dosing (≥13 years)
Treatment:
- Standard dose: 75 mg orally twice daily for 5 days 1, 2, 3
- Initiate within 48 hours of symptom onset for maximum benefit, though treatment beyond 48 hours still provides substantial benefit in hospitalized and high-risk patients 2
- May be taken with or without food, though administration with food improves gastrointestinal tolerability 1, 3
Prophylaxis:
- Post-exposure: 75 mg once daily for 10 days (initiate within 48 hours of exposure) 1, 2, 3
- Seasonal prophylaxis: 75 mg once daily for up to 6 weeks during community outbreaks 3
- Immunocompromised patients: May continue for up to 12 weeks 3
Pediatric Dosing (≥1 year to 12 years)
Weight-based dosing is essential for children ≥1 year: 1, 2, 3
| Body Weight | Treatment Dose (twice daily × 5 days) | Prophylaxis Dose (once daily × 10 days) | Oral Suspension Volume (6 mg/mL) |
|---|---|---|---|
| ≤15 kg (≤33 lb) | 30 mg | 30 mg | 5 mL |
| >15-23 kg (>33-51 lb) | 45 mg | 45 mg | 7.5 mL |
| >23-40 kg (>51-88 lb) | 60 mg | 60 mg | 10 mL |
| >40 kg (>88 lb) | 75 mg | 75 mg | 12.5 mL |
Infant Dosing (<1 year)
For term infants 0-8 months:
- Treatment: 3 mg/kg per dose twice daily for 5 days 1, 2, 3
- Prophylaxis: 3 mg/kg once daily for 10 days (for infants 3-11 months only) 1, 2
For infants 9-11 months:
Critical caveat: Prophylaxis is not recommended for infants <3 months unless the situation is judged critical due to limited safety data 1, 2
Preterm Infant Dosing
Preterm infants require substantially lower doses based on postmenstrual age (PMA = gestational age + chronological age) due to immature renal function: 1, 2, 6
| Postmenstrual Age | Treatment Dose (twice daily × 5 days) |
|---|---|
| <38 weeks PMA | 1.0 mg/kg per dose |
| 38-40 weeks PMA | 1.5 mg/kg per dose |
| >40 weeks PMA | 3.0 mg/kg per dose |
Common pitfall: Never use standard term infant dosing for preterm infants—this can lead to drug accumulation and toxicity 6
Renal Impairment Adjustments
For creatinine clearance 10-30 mL/min (moderate-to-severe renal impairment): 4, 1, 2, 3
Treatment:
Prophylaxis:
Important consideration: The most critical factor in older adults is renal function, not age alone—dose reductions are mandatory when creatinine clearance falls below 30 mL/min 1
Contraindication: Oseltamivir is not recommended for end-stage renal disease patients not undergoing dialysis 1, 3
Formulation and Administration
Available formulations: 1, 2, 3
- Capsules: 30 mg, 45 mg, 75 mg
- Oral suspension: 6 mg/mL when reconstituted (preferred for patients who cannot swallow capsules)
Administration pearls:
- Take with food to reduce nausea and vomiting (occurs in 5-15% of patients) 1, 3
- Capsules can be opened and contents mixed with liquid if needed 1
- If commercial suspension unavailable, pharmacies can compound suspension based on package insert instructions 1
Special Populations
Pregnancy:
- Same dosing as non-pregnant adults: 75 mg twice daily for treatment 2
- No dose adjustment needed throughout all trimesters or postpartum period 2
- Oseltamivir is preferred over zanamivir in pregnancy 2
- Breastfeeding is not a contraindication 2
Immunocompromised patients:
- Treat regardless of time since symptom onset 2
- May require extended treatment duration beyond 5 days if illness is prolonged 2
- Prophylaxis may be continued for up to 12 weeks 3
Drug Interactions
Live attenuated influenza vaccine (LAIV):
- Avoid LAIV within 48 hours before oseltamivir administration 1, 2
- Do not use oseltamivir for 14 days after LAIV vaccination 1, 2
Critical Timing Considerations
Treatment:
- Initiate within 48 hours of symptom onset for maximum benefit (reduces illness duration by 1-1.5 days) 2, 7
- Do not delay treatment while awaiting laboratory confirmation in high-risk patients 2
- Treatment after 48 hours still provides substantial benefit in hospitalized and high-risk patients 2
Prophylaxis:
- Initiate within 48 hours of exposure to infected individual 2, 3
- Protection lasts only as long as dosing is continued 3
Common Pitfalls to Avoid
- Do not confuse GFR with creatinine clearance when calculating renal dosing adjustments 6
- Do not use standard term infant dosing for preterm infants—they require significantly lower postmenstrual age-based dosing 1, 6
- Do not withhold treatment in high-risk patients presenting beyond 48 hours—they still derive substantial benefit 2
- Do not use weight-based dosing approved for older children in infants <1 year—they require mg/kg dosing 1, 2, 5