Strattera (Atomoxetine) Dosage and Treatment Plan for ADHD
For the treatment of ADHD, Strattera (atomoxetine) should be initiated at 40 mg daily and titrated to a target dose of 80 mg daily (or 1.2 mg/kg/day for those under 70 kg), with a maximum dose of 100 mg daily or 1.4 mg/kg/day. 1
Dosing Guidelines
Initial Dosing
- Children and adolescents up to 70 kg: Start with 0.5 mg/kg/day
- Children and adolescents over 70 kg and adults: Start with 40 mg/day 1
- Dose can be administered once daily in the morning or divided into two doses (morning and late afternoon) 1, 2
Titration
Target and Maximum Doses
- Target dose:
- Children and adolescents up to 70 kg: 1.2 mg/kg/day
- Children and adolescents over 70 kg and adults: 80 mg/day 1
- Maximum dose:
- Children and adolescents up to 70 kg: 1.4 mg/kg/day
- Children and adolescents over 70 kg and adults: 100 mg/day 1
Administration Considerations
- Can be administered as a single daily dose in the morning or divided into two evenly distributed doses 1, 2
- Once-daily dosing has been shown to be effective and convenient 4
- Twice-daily dosing may reduce the incidence of nausea (16.4% vs 32.4% with once-daily dosing) 2
- Can be taken with or without food 1
- No need for drug holidays (unlike stimulants) due to 24-hour coverage of symptoms 4
Special Populations
CYP2D6 Poor Metabolizers
- Approximately 7% of the population are poor CYP2D6 metabolizers 5
- These individuals may require lower doses due to slower clearance of atomoxetine 6
- Plasma concentrations can be approximately 10-fold higher in poor metabolizers 6
Hepatic Impairment
- Dose adjustment required in moderate to severe hepatic impairment 1
- Monitor for signs of liver injury (jaundice, dark urine, right upper quadrant pain) 1
Patients with Substance Use Disorder
- Atomoxetine is recommended as first-line treatment for ADHD in patients with substance use disorder due to minimal abuse potential 5
- Not a controlled substance, making it suitable for patients with history of substance abuse 7
Monitoring and Follow-up
- Initial titration phase: Weekly contact (can be by telephone) 3
- Maintenance phase: Monthly appointments until symptoms stabilize 3
- Monitor for:
Efficacy and Duration of Treatment
- Efficacy has been demonstrated in multiple randomized, double-blind, placebo-controlled trials 4
- Effects persist throughout waking hours and into the next morning with a single morning dose 4
- Long-term efficacy has been demonstrated for up to 18 months 4
- Atomoxetine improves core ADHD symptoms as well as quality of life measures and self-esteem 4
Common Side Effects
- Gastrointestinal disorders (nausea, dry mouth)
- Decreased appetite
- Insomnia
- Dizziness
- Sweating
- Sexual problems
- Modest increases in heart rate and blood pressure 7
Important Precautions
- Boxed warning: Increased risk of suicidal ideation in children and adolescents 1
- Cardiovascular: Not recommended in patients with serious structural cardiac abnormalities or other serious cardiac problems 1
- Liver: Discontinue if jaundice or laboratory evidence of liver injury occurs 1
- Urinary: May cause urinary hesitancy or retention 1
- Priapism: Requires prompt medical attention if suspected 1
Atomoxetine is a valuable non-stimulant option for ADHD treatment with the advantage of once-daily dosing, 24-hour symptom coverage, and no abuse potential, making it particularly suitable for patients with substance abuse concerns or those who prefer not to take controlled substances.