What is the recommended dosage of Strattera (atomoxetine) for patients with Attention Deficit Hyperactivity Disorder (ADHD)?

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Strattera (Atomoxetine) Dosage for ADHD

Start atomoxetine at 40 mg orally once daily, then titrate every 7-14 days to 60 mg and then 80 mg daily, with a maximum dose of 1.4 mg/kg/day or 100 mg/day, whichever is less. 1

Initial Dosing

  • Begin with 40 mg orally once daily as the standard starting dose 1
  • Atomoxetine can be administered as either a single daily dose or split into two evenly divided doses throughout the day 2, 3
  • A single morning dose provides symptom control extending throughout waking hours and into the next morning 4

Titration Schedule

  • Adjust the dose every 7-14 days based on clinical response and tolerability 1
  • Progress from 40 mg daily to 60 mg daily, then to 80 mg daily 1
  • The target therapeutic dose is approximately 1.2 mg/kg/day 4
  • Maximum dose is the lesser of 1.4 mg/kg/day or 100 mg/day 1

Monitoring During Titration

  • Maintain weekly contact (by telephone is acceptable) during initial titration and dose adjustments 5
  • Titration typically requires 2-4 weeks to reach optimal dosing 5
  • Systematically assess for specific side effects including insomnia, anorexia, headaches, decreased appetite, nausea, abdominal pain, and somnolence at each adjustment 5, 2
  • Monitor weight regularly as weight loss is common with atomoxetine 5
  • Check heart rate and blood pressure, as modest increases may occur but are generally well tolerated 2, 3

Onset of Effect and Long-Term Management

  • Allow 6-12 weeks for full therapeutic effects to be observed, as atomoxetine has a slower onset compared to stimulants 1
  • After dose stabilization, schedule follow-up appointments at least monthly 5
  • If adequate symptom control is not achieved at maximum dose, consider alternative treatments or adding non-stimulant medications 5

Special Populations

Adults with ADHD

  • Use the same dosing strategy: 60,90, or 120 mg/day in divided or single doses 6, 3
  • Adult trials demonstrated efficacy at these doses with good tolerability 6, 3

Poor CYP2D6 Metabolizers

  • Patients who are poor CYP2D6 metabolizers have greater drug exposure and slower elimination 2
  • These patients may require lower doses and experience more adverse effects 2
  • CYP2D6 inhibitors (such as paroxetine) produce similar pharmacokinetic changes 2

Clinical Context

  • Atomoxetine is generally used as second-line therapy after stimulants in most guidelines, though it may be first-line in specific circumstances 1
  • Consider atomoxetine as first-line in patients with comorbid substance use disorders, tic/Tourette's disorder, anxiety, or those who prefer a non-controlled substance 1, 2, 7
  • Atomoxetine has negligible abuse potential and is not a controlled substance 2, 6, 3

Common Pitfalls to Avoid

  • Do not start at too high a dose, as this increases unnecessary side effects and decreases adherence 5
  • Do not expect immediate results—unlike stimulants, atomoxetine requires 6-12 weeks for full effect 1
  • Do not discontinue abruptly without assessment, though atomoxetine is not associated with rebound symptoms or acute discontinuation syndrome 2, 4
  • Be aware of the black-box warning for suicidal ideation, particularly during initial treatment 2
  • Monitor for rare but serious liver injury, though this is uncommon 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.

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