What is the recommended starting dose for initiating atomoxetine (Strattera) therapy?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 22, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Atomoxetine Initial Dosing Recommendations

For children and adolescents up to 70 kg, atomoxetine should be initiated at 0.5 mg/kg/day, while adults and children over 70 kg should start at 40 mg daily. 1, 2

Detailed Dosing Guidelines

Initial Dosing

  • Children and adolescents ≤70 kg: 0.5 mg/kg/day 1, 2
  • Adults and children >70 kg: 40 mg daily 1, 2

Titration Schedule

  • Increase dose after a minimum of 3 days 2
  • Target doses:
    • Children and adolescents ≤70 kg: 1.2 mg/kg/day 1, 2
    • Adults and children >70 kg: 80 mg daily 1, 2

Maximum Doses

  • Children and adolescents ≤70 kg: 1.4 mg/kg/day or 100 mg daily (whichever is less) 1, 2
  • Adults and children >70 kg: 100 mg daily 1, 2

Administration Considerations

  • Can be administered as a single daily dose in the morning or divided into two doses (morning and late afternoon/early evening) 2
  • May be taken with or without food 2
  • Capsules should be swallowed whole, not opened 2

Special Populations

Hepatic Impairment

  • Moderate impairment (Child-Pugh Class B): Reduce initial and target doses to 50% of normal dose 1, 2
  • Severe impairment (Child-Pugh Class C): Reduce initial and target doses to 25% of normal dose 1, 2

CYP2D6 Poor Metabolizers or Patients Taking CYP2D6 Inhibitors

  • Children and adolescents ≤70 kg: Start at 0.5 mg/kg/day; increase to 1.2 mg/kg/day only if symptoms don't improve after 4 weeks and initial dose is well tolerated 2
  • Adults and children >70 kg: Start at 40 mg/day; increase to 80 mg/day only if symptoms don't improve after 4 weeks and initial dose is well tolerated 2

Monitoring and Follow-up

  • Monitor for common side effects, particularly:
    • Gastrointestinal effects (most common adverse event) 1, 3
    • Suicidal ideation, especially during first months of treatment 1
    • Blood pressure and heart rate changes 1
    • Hepatic function 1

Efficacy Considerations

  • No additional benefit has been demonstrated for doses higher than 1.2 mg/kg/day 2
  • Atomoxetine shows a graded dose-response, with 1.2 mg/kg/day appearing to be as effective as 1.8 mg/kg/day for most patients 4
  • Lower maintenance doses (0.5 mg/kg/day) may be effective for long-term treatment after initial response to higher doses 5

Clinical Pearls

  • Atomoxetine is not a controlled substance and has negligible risk of abuse 6
  • Full therapeutic effect may take several weeks to develop, unlike stimulants which work more rapidly
  • Screen for bipolar disorder before initiating treatment 2
  • Approximately 7% of the population are poor CYP2D6 metabolizers who may require lower doses 1

Remember that atomoxetine is indicated as part of a comprehensive treatment program that may include psychological, educational, and social interventions 2.

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.