Abstract
Atomoxetine is a nonstimulant medication used to treat attention-deficit/hyperactivity disorder (ADHD). Cytochrome P450 (CYP)2D6 polymorphisms influence the metabolism of atomoxetine thereby affecting drug efficacy and safety. We summarize evidence from the published literature supporting these associations and provide therapeutic recommendations for atomoxetine based on CYP2D6 genotype (updates at www.cpicpgx.org).
© 2019 The Authors Clinical Pharmacology & Therapeutics © 2019 American Society for Clinical Pharmacology and Therapeutics.
Publication types
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Research Support, N.I.H., Extramural
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Practice Guideline
MeSH terms
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Adrenergic Uptake Inhibitors / administration & dosage
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Adrenergic Uptake Inhibitors / adverse effects
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Adrenergic Uptake Inhibitors / pharmacokinetics*
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Adrenergic Uptake Inhibitors / therapeutic use*
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Atomoxetine Hydrochloride / administration & dosage
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Atomoxetine Hydrochloride / adverse effects
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Atomoxetine Hydrochloride / pharmacokinetics*
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Atomoxetine Hydrochloride / therapeutic use*
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Attention Deficit Disorder with Hyperactivity / drug therapy*
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Cytochrome P-450 CYP2D6 / genetics*
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Dose-Response Relationship, Drug
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Genetic Testing / methods
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Genetic Testing / standards
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Genotype
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Humans
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Pharmacogenetics
Substances
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Adrenergic Uptake Inhibitors
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Atomoxetine Hydrochloride
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Cytochrome P-450 CYP2D6