Foquest vs. Concerta: Key Differences for ADHD Treatment
Both Foquest and Concerta are extended-release methylphenidate formulations that provide 12-hour symptom control with once-daily dosing, but they differ in their drug delivery systems and pharmacokinetic profiles, which may allow physicians to match formulations to individual patient symptom patterns throughout the day. 1, 2
Core Similarities
Both medications are:
- First-line pharmacological treatments for ADHD in children, adolescents, and adults 1
- Extended-release methylphenidate formulations designed for once-daily administration 1, 2
- Effective for approximately 12 hours of symptom coverage 2, 3
- Associated with similar adverse effect profiles including appetite suppression, insomnia, headache, and abdominal pain 4, 3
- Controlled substances (Schedule II) with abuse potential requiring careful monitoring 4
Critical Differences in Drug Delivery Systems
Concerta's OROS Technology
- Utilizes an osmotic-release oral system (OROS) that produces an ascending plasma drug level pattern throughout the day 2, 3
- Begins working within 1-2 hours with effects lasting the full 12-hour period 2
- The OROS delivery system is specifically designed and FDA-approved; generic non-OROS formulations have demonstrated significantly reduced efficacy (mean T-score reduction of 23 points when switching from non-OROS to brand OROS, p<0.0001) 5
- Available in 18 mg, 36 mg, and 54 mg strengths 2
Foquest's Delivery System
- Listed alongside Concerta as an extended-release methylphenidate option in Canadian guidelines 1
- Specific pharmacokinetic profile differs from Concerta's OROS system 6
Pharmacokinetic Profile Implications
The different delivery systems create distinct plasma concentration curves that may suit different symptom patterns: 6
- Concerta's ascending pattern may benefit patients who need progressively increasing coverage throughout the school/work day 2, 3
- Extended-release formulations differ in "peak plasma levels and the rate at which peak levels are attained and decline" 6
- These pharmacokinetic differences provide opportunity to prescribe a formulation best suited to individual symptom profiles, though all maintain therapeutic concentrations during school/work hours 6
Dosing Considerations
Concerta-Specific Dosing
- 18 mg Concerta approximately equals methylphenidate 5 mg three times daily 2
- Adults often require higher total daily doses than children due to longer workday coverage needs 2
- Maximum typical dose is 72 mg, though higher doses may be used if documented as necessary 2
General Methylphenidate Dosing
- Start low (10-15 mg/day) and titrate by 10-15 mg weekly intervals to maximum 60 mg/day for immediate-release equivalents 3
- Weight does not predict optimal dosing; individual behavioral response is highly variable 3
- Plasma concentration monitoring is not clinically useful 3
Clinical Decision-Making Algorithm
When choosing between Foquest and Concerta:
Both are appropriate first-line options for ADHD treatment in patients ≥6 years old 1, 4
Consider Concerta specifically when:
Consider formulation differences for:
Important Safety Considerations
Both medications carry identical warnings: 4
- High abuse and misuse potential; assess risk before initiating treatment 4
- Contraindicated with MAOIs or within 14 days of MAOI use 4
- Risk of sudden death in patients with serious heart disease; cardiac screening required 4
- Monitor blood pressure and heart rate regularly 4
- Screen for psychiatric symptoms including psychosis, mania, and suicidal ideation 4
Common Pitfalls to Avoid
- Do not assume generic "Concerta" is equivalent—only OROS formulations demonstrate full efficacy 5
- Do not expect immediate onset—both require 1-2 hours to begin working 2
- Do not use weight-based dosing—titrate based on clinical response 3
- Do not abruptly discontinue if used long-term due to physical dependence risk 4
- Morning administration is essential to minimize sleep disturbances 2
Special Population Considerations
Pregnancy and Lactation
- Methylphenidate (both formulations) does not appear associated with major congenital malformations 1
- Small possible increased risks for cardiac malformations (OR 1.59) and preeclampsia (aRR 1.29), though other studies have not confirmed these associations 1
- Passes into breast milk; monitor infants for irritability, insomnia, and feeding difficulties 1