Contraindicated in:
Use Cautiously in:
May ↑ risk of suicide attempt/ideation especially during dose early treatment or dose adjustment; risk may be greater in children or adolescents
;CV: hypertension, orthostatic hypotension, QT interval prolongation, syncope, tachycardia
Derm: ↑sweating, rash, urticaria
GI: nausea, vomiting, dyspepsia, HEPATOTOXICITY, Adultsconstipation, dry mouth
GU: Adultsdysmenorrhea, ejaculatory problems, erectile dysfunction, libido changes, priapism, urinary hesitation, urinary retention
MS: RHABDOMYOLYSIS
Neuro: dizziness, fatigue, insomnia, mood swings, aggression, behavioral disturbances, delusions, hallucinations, hostility, mania, paresthesia, SUICIDAL THOUGHTS, thought disorder
Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS AND ANGIOEDEMA)
Drug-drug:
Hepatic Impairment
Therapeutic Classification: Agents for Attention-Deficit/Hyperactivity Disorder (ADHD)
Pharmacologic Classification: selective norepinephrine reuptake inhibitors
Absorption: Well absorbed following oral administration.
Distribution: Unknown.
Protein Binding: 98%.
Half-Life: 5 hr.
Advise patient and/or caregiver to notify health care provider if thoughts about suicide or dying, attempts to commit suicide, new or worse depression, new or worse anxiety, feeling very agitated or restless, panic attacks, trouble sleeping, new or worse irritability, acting aggressive or hostile, being angry or violent, acting on dangerous impulses, an extreme ↑ in activity and talking, or other unusual changes in behavior or mood occur or if signs and symptoms of severe liver injury (pruritus, dark urine, jaundice, right upper quadrant tenderness, unexplained flu-like symptoms) occur.
NDC Code