Lisdexamfetamine dimesylate

(Vyvanse®)

Lisdexamfetamine dimesylate

Drug updated on 9/4/2024

Dosage FormCapsule (oral; 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg); Chewable tablet (oral; 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg)
Drug ClassCentral nervous system stimulants
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients 6 years and older.
  • Indicated for the treatment of moderate to severe binge eating disorder (BED) in adults.

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Summary
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  • Vyvanse (lisdexamfetamine dimesylate) is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients 6 years and older, as well as for the treatment of moderate to severe binge eating disorder (BED) in adults.
  • This summary is based on the review of three systematic review(s)/meta-analysis(es). [1-3]
  • Lisdexamfetamine (LDX) is effective in treating Binge-Eating Disorder (BED), consistently reducing BED symptoms and body weight in patients.
  • In adults with Attention-Deficit Hyperactivity Disorder (ADHD), LDX demonstrated the highest effect size in reducing ADHD symptoms (SMD = -0.89) compared to mixed amphetamine salts (SMD = -0.64) and methylphenidate (SMD = -0.50), indicating superior efficacy among psychostimulants.
  • No significant differences in serious adverse events were found between ADHD pharmacotherapies (including LDX) and placebo, although a higher proportion of participants withdrew due to adverse events in the pharmacotherapy group.
  • There were no specific safety outcomes or adverse effects detailed for LDX in the treatment of Binge-Eating Disorder (BED).
  • Few randomized controlled trials (RCTs) reported on long-term adverse events.
  • There is no population types or subgroups information available in the reviewed studies.

Product Monograph / Prescribing Information

Document TitleYearSource
Vyvanse (lisdexamfetamine dimesylate) Prescribing Information.2023Takeda Pharmaceuticals America, Inc., Lexington

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines