Methylphenidate Dosing for ADHD
Start methylphenidate at a low dose and titrate systematically to the maximum effective dose that controls symptoms without intolerable adverse effects, rather than calculating dose by weight—this approach achieves optimal response in approximately 70% of patients. 1
Starting Doses
Immediate-Release Methylphenidate
- Begin with 5 mg twice daily (morning and midday) in children aged 6 years and older 2, 3
- For adults, start with 5–20 mg three times daily 2
- Administer doses 4–6 hours apart, with the last dose no later than early afternoon to minimize insomnia 3
Extended-Release Formulations
- Start with 18 mg once daily in the morning for OROS-methylphenidate (Concerta) 2
- Extended-release products provide 8–12 hours of symptom coverage, eliminating the need for school-day dosing 3
- The OROS system delivers approximately 12 hours of continuous release through osmotic-pump technology 2
Titration Protocol
Increase the dose by 5–10 mg weekly (for immediate-release) or by 18 mg weekly (for OROS formulations) based on symptom response and tolerability 1, 3
- Stimulant effects appear rapidly, allowing titration on a 7-day basis; in urgent situations, doses may be adjusted every 3 days 1
- Do not calculate dose based on mg/kg—variations in response are not related to height or weight 1
- Obtain weekly symptom ratings from parents, teachers, or the patient during dose adjustment to assess both efficacy and adverse effects 2, 4
- Continue titration until symptoms are optimally controlled or dose-limiting adverse effects emerge 1, 5
Maximum Daily Doses
Children and Adolescents
- Maximum 60 mg/day for immediate-release methylphenidate, regardless of formulation 3
- Maximum 54–72 mg/day for OROS-methylphenidate (Concerta) 2
- Doses above 60 mg/day are rarely needed in pediatric patients 2
Adults
- Maximum 60 mg/day for immediate-release methylphenidate (20 mg three times daily) 2, 3
- Maximum 60 mg/day for extended-release formulations 2
- Typical therapeutic range for adults is 30–37.5 mg/day, with maximum doses up to 60 mg/day 2
Critical Monitoring During Titration
- Measure blood pressure and pulse at baseline and at every dose adjustment 2, 4
- Monitor height and weight at each visit, particularly in children, as chronic stimulant use can suppress growth by approximately 1–2 cm from predicted adult height 2, 6
- Systematically assess for appetite suppression, insomnia, headaches, and abdominal pain—the most common dose-limiting adverse effects 2, 3, 6
- Track sleep quality and appetite changes throughout treatment 2, 4
Evidence for Dose Optimization
Flexible titration to higher doses based on symptom control and tolerability is associated with both improved efficacy and acceptability, because practitioners can adjust doses based on ADHD symptom response and the presence of adverse effects 5
- The incremental benefits of methylphenidate remain constant across the FDA-licensed dose range when flexible titration is used 5
- In fixed-dose trials, incremental benefits decrease beyond 30 mg of methylphenidate-equivalent dose, but flexible-dose trials demonstrate continued benefit with dose increases 5
- Approximately 70–80% of children and adolescents achieve optimal response when systematic dose-titration protocols are applied 1, 2
Common Pitfalls to Avoid
- Do not underdose—community treatment with lower doses and less frequent monitoring produces inferior results compared to optimal medication management 1
- Do not assume the current dose is adequate if impulsivity or other core symptoms persist—aggressive dose optimization is warranted 2
- Do not add a second medication before maximizing the methylphenidate dose 2
- Starting at too high a dose leads to unnecessary adverse effects and decreased adherence 4
- If adequate response is not achieved after proper titration of methylphenidate, trial an amphetamine-based stimulant—approximately 40% of patients respond to only one stimulant class 2
Special Populations
Children with Intellectual Disability
- Optimal dosing of methylphenidate (0.5–1.5 mg/kg/day) is practical and effective in children with hyperkinetic disorder and intellectual disability (IQ 30–69) 7
- Titrate through low (0.5 mg/kg/day), medium (1.0 mg/kg/day), and high dose (1.5 mg/kg/day) over at least 1 week each 7
- Effect sizes are smaller (0.39–0.52) compared to typically developing children, but 40% show clinical improvement 7
Children with Pervasive Developmental Disorders
- Use doses approximating 0.125,0.25, and 0.5 mg/kg per dose twice daily, with an additional half-dose in late afternoon 8
- Improvement is most evident at 0.25 and 0.5 mg/kg doses, with significant interindividual variability in dose response 8
- Hyperactivity and impulsivity improve more than inattention 8
Long-Term Safety
Two-year treatment with methylphenidate shows no evidence of clinically significant growth reduction, though pulse rate and blood pressure are modestly elevated and require regular monitoring 6