What is the recommended treatment and dosage for Attention Deficit Hyperactivity Disorder (ADHD) using Strattera (atomoxetine)?

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Last updated: October 14, 2025View editorial policy

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Strattera (Atomoxetine) Treatment for ADHD

For children and adolescents with ADHD, Strattera (atomoxetine) should be initiated at 0.5 mg/kg/day and titrated after a minimum of 3 days to a target dose of 1.2 mg/kg/day, with a maximum recommended dose of 1.4 mg/kg/day or 100 mg daily, whichever is less. 1

Dosage Recommendations

  • Atomoxetine is administered orally and is available in capsules containing 10,18,25,40,60,80, or 100 mg of atomoxetine hydrochloride, as well as in an oral solution (4 mg/ml) 2
  • For children and adolescents up to 70 kg: Start with 0.5 mg/kg/day, target 1.2 mg/kg/day, maximum 1.4 mg/kg/day 1, 3
  • For children and adolescents over 70 kg and adults: Start with 40 mg/day, target 80 mg/day, maximum 100 mg/day 3
  • Atomoxetine can be administered either as a single daily dose or split into two evenly divided doses 4
  • Dose titration should follow a sequential, weight-based approach 2

Age-Specific Recommendations

  • For preschool-aged children (4-5 years): Atomoxetine is not recommended as it has not received sufficient rigorous study in this population 1
  • For elementary school-aged children (6-11 years): Atomoxetine is FDA-approved, with evidence being sufficient but less strong than for stimulant medications 2
  • For adolescents (12-18 years): Atomoxetine is recommended with the adolescent's assent 2
  • Atomoxetine may be particularly useful for adolescents at risk of substance abuse, as it has negligible abuse potential and is not a controlled substance 2, 4

Safety Monitoring and Precautions

  • Atomoxetine carries an FDA black box warning for increased risk of suicidal ideation in children and adolescents 1, 3
  • Monitor closely for suicidality, clinical worsening, and unusual behavior changes, especially during the first few months of treatment or with dose changes 1, 3
  • Common adverse effects include:
    • Gastrointestinal symptoms (nausea, vomiting, abdominal pain) 2, 4
    • Decreased appetite 2, 4
    • Fatigue and somnolence 2, 4
  • Perform cardiac evaluation if risk factors are present before starting treatment 1
  • Monitor growth as atomoxetine has been linked to growth delays in the first 1-2 years of treatment 1
  • Monitor for hepatic effects, as atomoxetine has been associated with rare cases of severe liver injury 3

Special Considerations

  • Atomoxetine is metabolized through the CYP2D6 pathway; dosage adjustments may be needed for poor metabolizers or when used with CYP2D6 inhibitors 2, 3
  • For patients with comorbid anxiety, tics, or substance use concerns, atomoxetine may be preferable to stimulants 2, 5
  • Atomoxetine may be less likely than stimulants to exacerbate sleep disorders 4
  • The duration of action extends throughout waking hours with effects persisting to the next morning with a single morning dose 6

Comparative Efficacy

  • Atomoxetine is significantly more effective than placebo for treating ADHD symptoms 4, 5
  • Atomoxetine is comparable to immediate-release methylphenidate but less effective than extended-release methylphenidate formulations and extended-release mixed amphetamine salts 4, 5
  • In patients who respond favorably to initial treatment, atomoxetine has been shown to be superior to placebo in maintaining long-term response (up to 18 months) 6

Common Pitfalls to Avoid

  • Failing to monitor for suicidal ideation, especially during the first few months of treatment 1, 3
  • Not accounting for CYP2D6 metabolism status, which can significantly affect drug levels 2, 3
  • Starting at too high a dose; always begin at 0.5 mg/kg/day and titrate gradually 1
  • Not allowing sufficient time for full therapeutic effect, as atomoxetine may take longer than stimulants to show maximum benefit 6
  • Overlooking potential drug interactions, particularly with selective serotonin reuptake inhibitors which can elevate serum atomoxetine levels 2

Atomoxetine represents an important non-stimulant option for ADHD treatment, particularly valuable for patients with concerns about stimulant abuse potential or those with comorbid anxiety or tic disorders 2, 5.

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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