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Atomoxetine (Strattera)

University of Pittsburgh · FDA-approved active Small molecule

Atomoxetine selectively inhibits the reuptake of norepinephrine in the brain, increasing norepinephrine levels in the prefrontal cortex and improving attention and executive function.

Atomoxetine selectively inhibits the reuptake of norepinephrine in the brain, increasing norepinephrine levels in the prefrontal cortex and improving attention and executive function. Used for Attention-deficit/hyperactivity disorder (ADHD) in children, adolescents, and adults, ADHD-related symptoms in patients with comorbid conditions.

At a glance

Generic nameAtomoxetine (Strattera)
SponsorUniversity of Pittsburgh
Drug classNorepinephrine reuptake inhibitor (NRI)
TargetNorepinephrine transporter (NET)
ModalitySmall molecule
Therapeutic areaPsychiatry / Neurology
PhaseFDA-approved

Mechanism of action

Atomoxetine is a selective norepinephrine reuptake inhibitor (NRI) that blocks the norepinephrine transporter, preventing the reabsorption of norepinephrine at the presynaptic terminal. This increases norepinephrine concentration in synaptic spaces, particularly in brain regions responsible for attention, impulse control, and executive function. Unlike stimulant medications, it does not directly release norepinephrine or dopamine and has minimal abuse potential.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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