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Hepatic injury and hepatic failure adverse events in 3,4-methylenedioxymethamphetamine users reported to the FDA Adverse Event Reporting System.

Tigran Makunts, Ruben Abagyan

Frontiers in psychiatry January 1, 2024 DOI: 10.3389/fpsyt.2024.1414622 via PubMed

Summary

AI-generated from the abstract

MDMA, currently being studied as a treatment for PTSD, is extensively metabolized by the liver, raising concerns about rare but serious drug-induced liver injury (DILI). While clinical trials have not measured liver injury markers or observed DILI symptoms, analysis of over 1,500 reports from the FDA Adverse Event Reporting System identified 23 cases of hepatic injury or failure where MDMA was taken with other substances. Twenty-two of those cases involved other drugs with known DILI concern, and only one report listed MDMA as the primary suspect. Given nearly 20 million annual doses of MDMA, this single report is insufficient to establish a significant association with DILI.

Study at a glance

Characteristics Observational study Peer reviewed
Sample size 1,500
Population Reports from the FDA Adverse Event Reporting System
Topics MDMA
Keywords Ddi drug-drug interaction Faers MDMA 3,4-Methylenedioxymethamphetamine Adverse events Drug safety
Citations 2
Key finding Analysis of over 1,500 adverse event reports found only one case where MDMA was the primary suspect in liver injury, insufficient to establish a significant association with DILI.

Abstract

3,4-Methylenedioxymethamphetamine (MDMA) is being investigated in controlled clinical trials for use as an adjunct medication treatment for post-traumatic stress disorder. MDMA is metabolized by N-demethylation, primarily by CYP2D6, to its main inactive metabolite, 4-hydroxy-3-methoxymethamphetamine. It is also metabolized to a lesser extent by CYP1A2, CYP2B6, and CYP3A4 to its active metabolite, 3,4-methylenedioxyamphetamine. Considering the extensive hepatic metabolism and excretion, MDMA use in psychiatry raises concerns over drug-induced liver injury (DILI), a rare but dangerous event. Majority of the drugs withdrawn from the market for liver injury caused death or transplantation at frequencies under 0.01%. Unfortunately, markers for liver injury were not measured in most published clinical trials. At the same time, no visible DILI-related symptoms and adverse events were observed. Idiosyncratic DILI cases are rarely registered during clinical trials due to their rare nature. In this study, we surveyed a larger, over 1,500, and a more diverse set of reports from the FDA Adverse Event Reporting System and found 23 cases of hepatic injury and hepatic failure, in which MDMA was reported to be taken in addition to one or more substances. Interestingly, 22 out of 23 cases had one or more listed drugs with a known DILI concern based on the FDA's DILIrank dataset. Furthermore, only one report had MDMA listed as the primary suspect. Considering the nearly 20 million doses of MDMA used annually, this single report is insufficient for establishing a significant association with DILI.

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