- selective norepinephrine reuptake inhibitor
- only FDA approved SNRI for adhd
- used as second-line therapy after trial of atl east 2 stimulant agents
- slower onset of action than stimulants (does not work immediately, takes ~2 weeks to see effect)
- no abuse potential
- less potential to cause growth effects in comparison to stimulant agents
- good for comorbid anxiety disorders, tics
- adverse effects: nausea, anorexia, insomnia, sedation, liver toxicity, priapism
- metabolized through cyp 2D6
- need to be dose reduced in hepatic impairment
- no renal dose adjustments
- potential for drug drug interactions with 2D6 inhibitors or inducers
- pathogenesis of ADHD: involved with hypoactivity of dopamine and norepinephrine in frontal-subcortical circuits in brain
- atomoxetine works strictly on norepinephrine
- other SNRIs (duloxetine and venlafaxine) work on serotonin and norepinephrine
- mostly work on serotonin, starts to work on norepinephrine only with HIGH doses
- more efficacious to use an SNRI that has more effect on norepinephrine vs serotonin as that is the catecholamine affected in ADHD
- there is weak evidence to use duloxetine in ADHD although not FDA approved for this use
- 1 RCT compared duloxetine to placebo showed some benefit, but further studies needed
- no RCTs comparing duloxetine to atomoxetine
Friday, November 18, 2016
atomoxetine for adhd
Atomoxetine: (why is this the most efficacious for adhd vs. other SNRIs?)
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