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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.
Abstract:
3,4-Methylenedioxymethamphetamine (MDMA) is currently being investigated as an adjunctive treatment to therapy for posttraumatic stress and other anxiety related disorders in clinical trials. Within the next few years MDMA-assisted therapy is projected for approval by regulatory authorities. MDMA's primary mechanism of action includes modulation of monoamine signaling by increasing release and inhibiting reuptake of serotonin, norepinephrine, and, to a lesser extent, dopamine. This pharmacology affects sympathomimetic physiology. In controlled trials, special attention has been given to cardiovascular adverse events (AEs), because transient increases in heart rate and blood pressure have been observed during the MDMA-assisted therapy sessions. Finding and quantifying the potential drivers of cardiac AEs in clinical trials is difficult since only a relatively small number of participants have been included in these studies, and a limited set of allowed concomitant drugs has been studied. In this study a more diverse set of reports from the FDA Adverse Event Reporting System was surveyed. We found 17 cases of cardiovascular AEs, in which the individuals had taken one or more substances in addition to MDMA. Interestingly, all of those concomitant medications and illicit substances, including opioids, stimulants, anticholinergics, and amphetamines, had been previously associated with cardiovascular AEs. Furthermore, in none of the reports MDMA was marked as the primary suspect.
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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