UBC Faculty Research and Publications

Atomoxetine for ADHD in children and adolescents Therapeutics Initiative (University of British Columbia)

Description

Therapeutics Letter 73 summarizes the evidence for atomoxetine for Attention-Deficit/Hypertactivity Disorder (ADHD) in children and adolescents. Conclusions: Short-term use (< 1 year): Based on RCTs < 8 weeks, atomoxetine reduces teacher and parent ratings of hyperactive/impulsive disruptive behaviour but the effect is less than that seen with methylphenidate and mixed amphetamine salts. Atomoxetine causes the following adverse effects in 5 to 15% of patients: decreased appetite, abdominal pain, vomiting and somnolence. Intermediate- to long-term use (>1 year): No RCTs are available. Effects on educational achievement are unknown. Atomoxetine adversely affects growth (weight and height) compared to national norms. Adverse consequences of the increased heart rate and blood pressure caused by atomoxetine are expected based on epidemiologic data.

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Attribution-NonCommercial-NoDerivatives 4.0 International