Concomitant medications associated with ischemic, hypertensive, and arrhythmic events in MDMA users in FDA adverse

Tigran Makunts1,2, Diane Dahill1, Lisa Jerome1

  • 1MAPS Public Benefit Corporation, San Jose, CA, United States.

PubMed

Insights

Concomitant drug use with 3,4-Methylenedioxymethamphetamine (MDMA) may increase cardiovascular risks. Analysis of FDA reports suggests other substances, not MDMA alone, were linked to adverse cardiac events in patients undergoing therapy.

Area of Science:

  • Psychopharmacology
  • Cardiovascular Safety
  • Regulatory Science

Background:

  • 3,4-Methylenedioxymethamphetamine (MDMA) shows promise for treating PTSD and anxiety disorders.
  • MDMA's mechanism involves monoamine signaling, potentially causing sympathomimetic effects.
  • Cardiovascular adverse events (AEs) are monitored in MDMA clinical trials due to transient heart rate and blood pressure increases.

Purpose of the Study:

  • To investigate potential drivers of cardiovascular AEs in patients using MDMA.
  • To analyze a broader range of adverse event reports than available in controlled trials.

Main Methods:

  • Surveyed the FDA Adverse Event Reporting System (FAERS) for cardiovascular AEs associated with MDMA use.
  • Identified cases where individuals took additional medications or illicit substances concurrently with MDMA.

Main Results:

  • Identified 17 cases of cardiovascular AEs in individuals using MDMA with other substances.
  • All concomitant substances (opioids, stimulants, anticholinergics, amphetamines) were previously linked to cardiovascular AEs.
  • MDMA was not identified as the primary suspect in any of the reported cases.

Conclusions:

  • Concomitant use of certain medications and illicit substances may contribute to cardiovascular AEs during MDMA-assisted therapy.
  • Further research is needed to fully understand the complex interactions and risks.
  • This highlights the importance of comprehensive medication review in patients undergoing MDMA therapy.

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