Pediatric Oseltamivir (Tamiflu) Dosing
Oseltamivir dosing in children is weight-based for those ≥12 months and mg/kg-based for infants <12 months, with treatment given twice daily for 5 days and prophylaxis once daily for 10 days. 1
Treatment Dosing (5 days, twice daily)
Children ≥12 months to 12 years (Weight-Based)
- ≤15 kg (≤33 lb): 30 mg twice daily = 5 mL of oral suspension 1, 2
- >15–23 kg (>33–51 lb): 45 mg twice daily = 7.5 mL of oral suspension 1, 2
- >23–40 kg (>51–88 lb): 60 mg twice daily = 10 mL of oral suspension 1, 2
- >40 kg (>88 lb): 75 mg twice daily = 12.5 mL of oral suspension 1, 2
Term Infants <12 months (mg/kg-Based)
- 9–11 months: 3.5 mg/kg per dose twice daily 1, 2
- 0–8 months (term infants): 3 mg/kg per dose twice daily 1, 2
Critical caveat: The CDC recommends 3 mg/kg twice daily for ALL infants <12 months, while the AAP differentiates between 0–8 months (3 mg/kg) and 9–11 months (3.5 mg/kg). 1 The 3.5 mg/kg dose for 9–11 month-olds is based on pharmacokinetic data showing this achieves target drug exposures in this age group. 3
Preterm Infants (Postmenstrual Age-Based)
Preterm infants require substantially lower doses due to immature renal function—using term infant dosing can lead to toxic drug concentrations. 1
- <38 weeks postmenstrual age: 1.0 mg/kg twice daily 1
- 38–40 weeks postmenstrual age: 1.5 mg/kg twice daily 1
- >40 weeks postmenstrual age: 3.0 mg/kg twice daily 1
For extremely preterm infants (<28 weeks postmenstrual age), consult a pediatric infectious disease specialist before initiating therapy. 1
Prophylaxis Dosing (10 days, once daily)
Children ≥12 months to 12 years
- Use the same weight-based doses as treatment, but once daily instead of twice daily for 10 days 1, 2
- ≤15 kg: 30 mg once daily 1
- >15–23 kg: 45 mg once daily 1
- >23–40 kg: 60 mg once daily 1
- >40 kg: 75 mg once daily 1
Infants 3–11 months
Infants <3 months
- Prophylaxis is NOT recommended for infants <3 months unless the situation is judged critical due to limited safety and efficacy data 1
Renal Impairment Adjustments
Dose adjustments are mandatory for creatinine clearance <60 mL/min to prevent toxicity. 1, 2
Treatment Dosing
Prophylaxis Dosing
- CrCl 10–30 mL/min: 30 mg once daily for 10 days OR 75 mg every other day for 10 days (5 total doses) 1, 2
Formulation and Administration
Oral Suspension
- Concentration: 6 mg/mL when reconstituted 1, 2
- Available as: 30 mg, 45 mg, and 75 mg capsules, plus powder for oral suspension 1, 2
- If commercial suspension unavailable: Pharmacies can compound a 6 mg/mL suspension by opening capsules and mixing contents with simple syrup or Ora-Sweet SF per package instructions 1
Measuring Devices
- For infants <12 months: Use a calibrated 3-mL or 5-mL oral syringe for accurate measurement of small volumes—the standard syringe supplied with commercial product is inadequate 4
- Never use household spoons for measurement 4
Timing and Food
- Administer with food to reduce nausea and vomiting, which occur in approximately 10% of patients 5, 4
- Initiate treatment within 48 hours of symptom onset for maximum effectiveness; earlier treatment (within 12–24 hours) provides substantially greater benefit 1, 6, 7
- Treatment started within 12 hours reduces illness duration by an additional 74.6 hours compared to treatment at 48 hours 7
Clinical Benefits
Oseltamivir reduces illness duration by approximately 1–1.5 days (26–36% reduction) when started early. 5
- Decreases severity of symptoms including cough, coryza, and fever 5
- Reduces risk of secondary complications, particularly acute otitis media, by 44% 5
- When started within 12 hours in children 1–3 years, reduces acute otitis media incidence by 85% 6
- Reduces parental work absenteeism by approximately 3 days 6
Common Pitfalls to Avoid
- Do NOT use weight-based categorical dosing (≤15 kg = 30 mg) for infants <12 months—this applies only to children ≥12 months 4
- Do NOT apply term infant dosing to preterm infants—postmenstrual age-based dosing is required to avoid toxicity 1
- Do NOT delay treatment waiting for laboratory confirmation during influenza season—clinical judgment is sufficient 8
- Do NOT stop therapy early even if symptoms improve before day 5—complete the full 5-day course to ensure adequate viral suppression 4
- Do NOT confuse treatment dosing (twice daily) with prophylaxis dosing (once daily) 8, 4
Special Populations
FDA Approval
- Approved for treatment in children as young as 2 weeks of age 1, 2
- Can be used from birth (including preterm infants) because benefits likely outweigh risks, though FDA approval is for ≥2 weeks 1
Immunocompromised Patients
- Prophylaxis may be continued for up to 12 weeks during community outbreaks 2