What is the recommended dosing when switching from Mydayis (amphetamine) 50mg to Vyvanse (lisdexamfetamine)?

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Switching from Mydayis 50mg to Vyvanse: Dosing Recommendations

When switching from Mydayis (mixed amphetamine salts) 50mg to Vyvanse (lisdexamfetamine), start with Vyvanse 50-60mg once daily in the morning, as both medications deliver similar amphetamine exposure and Vyvanse is dosed up to 70mg daily for ADHD. 1

Rationale for Dose Conversion

Mydayis 50mg and Vyvanse 50-60mg provide comparable amphetamine delivery:

  • Lisdexamfetamine is a prodrug that converts to dextroamphetamine after oral ingestion through enzymatic hydrolysis, with the conversion being rate-limited and gradual 2, 3
  • Vyvanse 100mg delivers equimolar amphetamine exposure to 40mg of immediate-release dextroamphetamine, meaning approximately 2.5:1 ratio of lisdexamfetamine to active amphetamine 3
  • The FDA-approved dosing range for Vyvanse in ADHD is 30-70mg daily, with dose adjustments in 10-20mg increments at weekly intervals 1

Recommended Switching Strategy

Direct switch approach (preferred for stable patients):

  • Discontinue Mydayis 50mg and initiate Vyvanse 50mg the following morning 1
  • Alternatively, start at Vyvanse 60mg if the patient requires robust symptom control throughout the day 1
  • Take Vyvanse in the morning with or without food; avoid afternoon dosing due to insomnia risk 1

Titration approach (if uncertain about equivalency):

  • Start Vyvanse at 40mg and increase by 10mg weekly based on response, up to maximum 70mg daily 1
  • This conservative approach minimizes risk of under- or over-dosing during transition 4

Pharmacokinetic Considerations

Vyvanse has a delayed onset compared to immediate-release amphetamines:

  • Peak amphetamine concentrations occur approximately 1 hour later with lisdexamfetamine versus immediate-release dextroamphetamine 3
  • The lag time for plasma concentration increase is 0.6 hours longer with lisdexamfetamine 3
  • Duration of effect extends to 14 hours post-dose in adults, providing all-day coverage 5

Monitoring During Transition

Assess the following parameters weekly during the first month:

  • ADHD symptom control throughout the day, particularly late afternoon/evening coverage 5
  • Blood pressure and heart rate at each visit (quarterly thereafter once stable) 6
  • Appetite and weight at each visit, as appetite suppression is dose-dependent 1
  • Sleep quality and insomnia symptoms, given morning-only dosing requirement 1
  • Emergence of irritability, anxiety, or mood changes 1

Common Pitfalls to Avoid

Do not start at 30mg Vyvanse when switching from Mydayis 50mg:

  • This represents significant under-dosing and will likely result in inadequate symptom control 1
  • The FDA recommends 30mg as a starting dose for stimulant-naive patients, not for those already on therapeutic amphetamine doses 1

Do not divide or split Vyvanse capsules for "in-between" doses:

  • The FDA explicitly states not to take less than one capsule per day and that a single dose should not be divided 1
  • If dose adjustment needed, use the available strengths (10,20,30,40,50,60, 70mg) 1

Do not administer Vyvanse in the afternoon:

  • Unlike Mydayis which may have been dosed differently, Vyvanse must be taken in the morning to avoid insomnia 1

Dose Adjustments Based on Response

If inadequate response at Vyvanse 50-60mg:

  • Increase to 70mg (maximum FDA-approved dose for ADHD) after at least one week 1
  • Allow minimum one week between dose increases to properly evaluate response 6

If excessive side effects occur:

  • Reduce dose by 10mg increments 1
  • Consider that peak subjective effects and cardiovascular stimulation are similar between equimolar doses of lisdexamfetamine and dextroamphetamine 3

References

Research

Lisdexamfetamine.

Paediatric drugs, 2007

Research

Rationale and strategies for switching antipsychotics.

American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists, 2002

Guideline

Adderall XR Dosage and Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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