Initial ADHD Medication Dosing
Recommended Starting Doses
For adults and children 6 years and older starting ADHD treatment, begin with methylphenidate 5 mg twice daily (after breakfast and lunch) or amphetamine/dextroamphetamine 2.5 mg once daily in the morning, then titrate upward weekly based on symptom response and tolerability. 1
Methylphenidate (MPH) Initiation
- Start with 5 mg given twice daily (after breakfast and lunch), with an optional third dose after school if needed for homework and social activities 1
- For adults, alternative starting dose is 5-10 mg in the morning after breakfast 2
- Increase by 5-10 mg increments weekly until symptoms improve or side effects emerge 1, 2
- Total daily doses typically range from 10-60 mg/day, though some adults may require up to 72 mg/day depending on formulation 1, 2
- Maximum benefit in fixed-dose trials occurs around 30 mg daily, though flexible titration allows for higher effective doses 3
Amphetamine/Dextroamphetamine (AMP/DEX) Initiation
- Start with 2.5 mg once daily in the early morning for children 1
- For adults, start with 10 mg once daily in the morning 2, 4
- Add a noon dose if symptom control doesn't last through the school/work day 1
- Increase by 5 mg weekly increments as needed 2, 4
- Maximum recommended dose is 40 mg/day for children and 50 mg/day for adults 1, 4
Lisdexamfetamine (Vyvanse) Initiation
- Start with 30 mg once daily in the morning for both adults and children 6 years and older 5
- Titrate in 10-20 mg increments at approximately weekly intervals 5
- Maximum recommended dose is 70 mg once daily 5
Weight-Based Dosing Considerations
Do not use weight-based dosing for initial titration - behavioral response is highly variable and not predicted by body weight 1, 6
- For children weighing less than 20 kg (45 lbs), omit the 15 mg dose step during methylphenidate titration 1
- Total daily MPH doses for children under 25 kg in clinical trials reached up to 35 mg 1
Titration Strategy: Fixed vs Flexible Dosing
Stepwise Titration (Preferred in Clinical Practice)
- Increase dose weekly based on symptom improvement and side effect profile 1
- Obtain standardized ADHD rating scales from teachers/parents for children, or from patient/significant other for adults before each increase 1
- Contact can be maintained by telephone during initial titration 7
- Stop titration when symptoms resolve and impairment diminishes, or when side effects become problematic 1
Forced Titration Trial (Alternative Method)
- Patient takes all four dose levels (5,10,15,20 mg of MPH or 2.5,7.5,10 mg of DEX/AMP) with each dose lasting 1 week 1
- At follow-up, review rating scales from all 4 weeks and select the dose with most benefit and fewest side effects 1
- This approach provides systematic comparison across dose levels 1
Pre-Treatment Assessment Requirements
Before initiating stimulants, perform the following mandatory assessments: 2, 4
- Cardiovascular screening: baseline blood pressure, pulse, and assessment for symptomatic cardiovascular disease 2, 4
- Family history: sudden death, ventricular arrhythmia, or cardiac disease 1
- Tic assessment: evaluate for motor/verbal tics or Tourette's syndrome 1
- Substance use screening: current or past substance abuse (relative contraindication requiring close supervision) 2
Monitoring During Titration
Schedule follow-up appointments at least monthly until symptoms stabilize 2, 7, 4
- Assess both therapeutic response and adverse effects at each dose adjustment using standardized rating scales 2, 7
- Monitor vital signs (blood pressure, pulse) with each dose increase 4
- Common adverse effects requiring monitoring: decreased appetite, gastrointestinal symptoms, sleep disturbances, increased blood pressure and heart rate 2
- Monitor weight regularly as weight loss is common with stimulants 7
- Systematically ask specific questions about known stimulant side effects such as insomnia, anorexia, and headaches 7
Timing of Administration
Administer stimulants in the morning to minimize sleep disturbances 4, 5
- Avoid afternoon doses of immediate-release formulations due to insomnia risk 5
- For immediate-release MPH, typical regimen is after breakfast and lunch, with optional third dose after school 1
- Afternoon doses may need to be higher than morning doses to prevent symptom attenuation later in the day 2
- Long-acting formulations provide 8-12 hours of coverage with once-daily dosing 2, 6
Critical Pitfalls to Avoid
Starting at excessively high doses increases adverse effects and reduces adherence - always begin conservatively 2, 4
- Do not increase doses too rapidly - allow minimum one week between adjustments to properly evaluate response 2, 4
- Failure to systematically assess both benefits and side effects during titration leads to suboptimal outcomes 7, 4
- Do not use plasma concentration monitoring - it is not clinically useful for methylphenidate 6
- Avoid abrupt discontinuation for "drug holidays" during important events as symptoms return rapidly 2
- Titrate slowly with small children and stop or reverse dose increases when side effects occur to maintain willingness to use stimulants 1
Special Populations
Older Adults
- More conservative titration recommended: increase by 5 mg every 2 weeks instead of weekly 4
- Older adults are more sensitive to both therapeutic and adverse effects due to age-related pharmacokinetic changes 4
- Careful monitoring of vital signs is particularly important in this population 4
Renal Impairment (for Lisdexamfetamine)
- Severe renal impairment (GFR 15-30 mL/min/1.73 m²): maximum 50 mg daily 5
- End-stage renal disease (GFR <15 mL/min/1.73 m²): maximum 30 mg daily 5
When to Consider Alternative Treatments
If adequate symptom control is not achieved at maximum dose, or intolerable side effects occur: 2, 4
- Switch to an alternative stimulant formulation (e.g., from methylphenidate to amphetamine or vice versa) before moving to non-stimulants 2
- Consider non-stimulant medications such as atomoxetine (starting at 40 mg/day, maximum 100 mg/day) or alpha-2 agonists as second-line options 2
- Reevaluate the diagnosis and consider comorbid conditions affecting treatment response 4
Evidence Quality Note
The dosing recommendations are based on high-quality guidelines from the American Academy of Child and Adolescent Psychiatry 1, 2 and FDA-approved labeling 5, with supporting evidence from meta-analyses demonstrating that flexible titration strategies allow for better efficacy and acceptability compared to fixed-dose approaches 3.