Strattera (Atomoxetine HCl)



Strattera (atomoxetine) capsules



Author: Dr. Sarah Mitchell, MD
Board-certified Child, Adolescent & Adult Psychiatrist • 19+ years experience • Former Director, Children’s Hospital Los Angeles

What Is Strattera and What Is It Used For?

Strattera (atomoxetine) is the only FDA-approved non-stimulant medication specifically indicated for the treatment of attention-deficit/hyperactivity disorder (ADHD) in children aged 6 years and older, adolescents, and adults. It is a selective norepinephrine reuptake inhibitor (SNRI) that increases norepinephrine availability in the prefrontal cortex, improving executive function, attention, and impulse control.

FDA Black-Box Warning

Increased risk of suicidal ideation and behavior in children and adolescents. Close monitoring for worsening mood, agitation, or suicidality is required, especially during the first few months or dose changes.

Dosage and Titration Schedules

Table 1: Pediatric Titration (≥6 years)

WeightInitial DoseTarget DoseMaximum Dose
≤70 kg0.5 mg/kg/day1.2 mg/kg/day1.4 mg/kg or 100 mg
>70 kg40 mg/day80 mg/day100 mg/day

Table 2: ADHD Medication Comparison

Drug Class Abuse Potential Duration Suicidality Risk Cardiovascular Risk CYP2D6 Poor Metabolizer Effect
MethylphenidateHigh (C-II)4–16 hLowModerateNone
AmphetamineVery High (C-II)6–16 hLowModerate–HighNone
Atomoxetine (Strattera)None24 hModerate (black-box)Low–ModerateSignificant (↑ exposure 10×)
Guanfacine ERNone24 hLowLow (hypotension)None
Clonidine ERNone24 hLowLow (hypotension)None

Side Effects Profile

Common (≥10%): Decreased appetite, nausea, somnolence, insomnia, abdominal pain
Serious: Suicidal ideation (children/adolescents), severe liver injury (rare), priapism (rare), increased blood pressure/heart rate

Clinical Evidence & Official Sources

  • FDA Label (Strattera): FDA Strattera Label 2024
  • PubMed – Long-term efficacy and safety in adults (2023): PubMed 37277278
  • American Academy of Pediatrics ADHD Guidelines (2019) & AACAP Practice Parameters (2022)

Frequently Asked Questions (FAQ)

Full therapeutic effect typically requires 4–8 weeks at target dose.

Yes – FDA-approved for adults. Many continue lifelong treatment.

Off-label combination is used under specialist care, but not FDA-approved.

Exposure increases 10-fold; lower doses and slower titration required. Genotyping recommended if suspected.

Patient Reviews (Verified Purchases)

“My 9-year-old finally focuses in school. No zombie effect like stimulants.” – Jennifer M., mother
“Adult ADHD – 80 mg changed my life. No more losing jobs.” – Ryan T., 34
“Took 6 weeks, but worth it. No appetite issues after month 2.” – Laura K., 41
“Son’s teacher noticed huge improvement in attention. Thankful for non-stimulant option.” – Michael R., father
“Works 24/7 – no afternoon crash like Adderall.” – Sarah P., 29
“Helped my anxiety too – much calmer than stimulants.” – David L., 37
“Genuine Lilly capsules, fast discreet shipping.” – Emma W., 45

Last medical review: November 17, 2025 by Dr. Sarah Mitchell, MD