What is the recommended dose of Tamiflu (oseltamivir) for a patient with influenza, considering factors such as age, weight, and impaired renal function?

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Last updated: January 20, 2026View editorial policy

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Oseltamivir (Tamiflu) Dosing Recommendations

Standard Adult and Adolescent Dosing (≥13 years)

For treatment of influenza, administer oseltamivir 75 mg orally twice daily for 5 days in adults and adolescents ≥13 years of age. 1, 2, 3

  • Initiate treatment within 48 hours of symptom onset for maximum benefit, which reduces illness duration by approximately 1-1.5 days 2, 4, 5
  • For prophylaxis, use 75 mg once daily for 10 days following exposure, or up to 6 weeks during community outbreaks 2, 4, 3
  • In immunocompromised patients, prophylaxis may be extended up to 12 weeks 3
  • Administration with food significantly reduces gastrointestinal side effects (nausea/vomiting), which occur in 10-15% of patients 2, 4

Pediatric Dosing (1-12 years)

Weight-based dosing is mandatory for children, with specific doses determined by body weight: 1, 2, 3

Treatment Dosing (twice daily for 5 days):

  • ≤15 kg: 30 mg twice daily 1, 3
  • >15-23 kg: 45 mg twice daily 1, 3
  • >23-40 kg: 60 mg twice daily 1, 3
  • >40 kg: 75 mg twice daily 1, 3

Prophylaxis Dosing (once daily for 10 days):

  • Use the same weight-based doses as treatment, but administered once daily instead of twice daily 1, 3

Infant Dosing (<1 year)

For term infants, dosing is age-based and calculated per kilogram of body weight: 1, 2

Term Infants (≥2 weeks to <1 year):

  • 0-8 months: 3 mg/kg per dose twice daily for treatment 1, 2, 3
  • 9-11 months: 3.5 mg/kg per dose twice daily for treatment 1, 2
  • Prophylaxis (3-8 months): 3 mg/kg once daily for 10 days 1
  • Prophylaxis is NOT recommended for infants <3 months unless the situation is judged critical 1

Preterm Infants (Critical Distinction):

Never use standard term infant dosing (3 mg/kg) for preterm infants—this leads to toxic drug accumulation due to immature renal function. 1

Dose preterm infants based on postmenstrual age (PMA = gestational age + chronological age): 1

  • <38 weeks PMA: 1.0 mg/kg per dose twice daily 1
  • 38-40 weeks PMA: 1.5 mg/kg per dose twice daily 1
  • >40 weeks PMA: 3.0 mg/kg per dose twice daily 1

Renal Impairment Dosing

Mandatory dose reductions are required for creatinine clearance <60 mL/min: 2, 4, 3

Adults with CrCl 10-30 mL/min:

  • Treatment: 30 mg once daily for 5 days (instead of 75 mg twice daily) 1, 2, 3
  • Prophylaxis: 30 mg once daily OR 75 mg every other day for 10 days (5 total doses) 1, 3

Pediatric Patients with CrCl 10-30 mL/min:

  • Reduce the child's weight-based dose to once daily (instead of twice daily) for 5 days 1
  • For prophylaxis, give half the standard once-daily dose given once daily, or the full once-daily dose every other day for 10 days 1

End-Stage Renal Disease:

  • Oseltamivir is not recommended for patients with end-stage renal disease not undergoing dialysis 3

Special Populations

Pregnant and Breastfeeding Women:

  • Use standard adult dosing: 75 mg twice daily for 5 days 2, 4
  • Breastfeeding is not a contraindication to oseltamivir use 2, 4

Elderly Patients (≥65 years):

  • Use standard adult dosing (75 mg twice daily) if renal function is normal 2
  • Mandatory dose reductions when creatinine clearance falls below 60 mL/min 2
  • Do not reduce dose based on age alone—assess renal function as it declines with aging 2

Formulation and Administration

  • Available as 30 mg, 45 mg, and 75 mg capsules and oral suspension (6 mg/mL when reconstituted) 1
  • The oral suspension is the preferred formulation for patients who cannot swallow capsules 3
  • Use an appropriate oral dosing dispensing device that accurately measures volume in mL 3
  • For infants <1 year, provide a dosing device that can accurately measure and administer small volumes 3

Critical Pitfalls to Avoid

Do not confuse treatment dosing (twice daily) with prophylaxis dosing (once daily)—this leads to underdosing treatment or overdosing prophylaxis. 2, 4

  • Never use weight-based dosing intended for children ≥1 year (30 mg, 45 mg, 60 mg, 75 mg unit doses) in infants <1 year—these doses are too high 1
  • Never confuse GFR with creatinine clearance when calculating renal dosing adjustments 1
  • Ensure infants are term (≥37 weeks gestation at birth)—if preterm, use postmenstrual age-based dosing 1
  • Do not withhold treatment in high-risk or hospitalized patients presenting beyond 48 hours of symptom onset 4

Clinical Efficacy Evidence

  • Standard-dose oseltamivir (75 mg twice daily for 5 days) was associated with an 82% reduction in odds of in-patient death in hospitalized patients with PCR-confirmed influenza B and A(H3N2) 6
  • No benefit has been demonstrated for double-dose oseltamivir therapy or extending treatment beyond 5 days in most patient populations 7
  • Oseltamivir may increase survival when used within 5 days of symptom onset in influenza H1N1-infected patients requiring ICU admission 7

References

Guideline

Oseltamivir Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Oseltamivir Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Oseltamivir Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Influenza treatment with oseltamivir outside of labeled recommendations.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2015

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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