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Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database
3,4-Methylenedioxymethamphetamine (MDMA) is currently being evaluated by the Food and Drug Administration (FDA) for the treatment of post-traumatic stress disorder (PTSD). If MDMA is FDA-approved it will be important to understand what medications may pose a risk of drug–drug interactions. The goal...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966744/ https://www.ncbi.nlm.nih.gov/pubmed/33727616 http://dx.doi.org/10.1038/s41598-021-85389-x |
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author | Cohen, Isaac V. Makunts, Tigran Abagyan, Ruben Thomas, Kelan |
author_facet | Cohen, Isaac V. Makunts, Tigran Abagyan, Ruben Thomas, Kelan |
author_sort | Cohen, Isaac V. |
collection | PubMed |
description | 3,4-Methylenedioxymethamphetamine (MDMA) is currently being evaluated by the Food and Drug Administration (FDA) for the treatment of post-traumatic stress disorder (PTSD). If MDMA is FDA-approved it will be important to understand what medications may pose a risk of drug–drug interactions. The goal of this study was to evaluate the risks due to MDMA ingestion alone or in combination with other common medications and drugs of abuse using the FDA drug safety surveillance data. To date, nearly one thousand reports of MDMA use have been reported to the FDA. The majority of these reports include covariates such as co-ingested substances and demographic parameters. Univariate and multivariate logistic regression was employed to uncover the contributing factors to the reported risk of death among MDMA users. Several drug classes (MDMA metabolites or analogs, anesthetics, muscle relaxants, amphetamines and stimulants, benzodiazepines, ethanol, opioids), four antidepressants (bupropion, sertraline, venlafaxine and citalopram) and olanzapine demonstrated increased odds ratios for the reported risk of death. Future drug–drug interaction clinical trials should evaluate if any of the other drug–drug interactions described in our results actually pose a risk of morbidity or mortality in controlled medical settings. |
format | Online Article Text |
id | pubmed-7966744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79667442021-03-19 Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database Cohen, Isaac V. Makunts, Tigran Abagyan, Ruben Thomas, Kelan Sci Rep Article 3,4-Methylenedioxymethamphetamine (MDMA) is currently being evaluated by the Food and Drug Administration (FDA) for the treatment of post-traumatic stress disorder (PTSD). If MDMA is FDA-approved it will be important to understand what medications may pose a risk of drug–drug interactions. The goal of this study was to evaluate the risks due to MDMA ingestion alone or in combination with other common medications and drugs of abuse using the FDA drug safety surveillance data. To date, nearly one thousand reports of MDMA use have been reported to the FDA. The majority of these reports include covariates such as co-ingested substances and demographic parameters. Univariate and multivariate logistic regression was employed to uncover the contributing factors to the reported risk of death among MDMA users. Several drug classes (MDMA metabolites or analogs, anesthetics, muscle relaxants, amphetamines and stimulants, benzodiazepines, ethanol, opioids), four antidepressants (bupropion, sertraline, venlafaxine and citalopram) and olanzapine demonstrated increased odds ratios for the reported risk of death. Future drug–drug interaction clinical trials should evaluate if any of the other drug–drug interactions described in our results actually pose a risk of morbidity or mortality in controlled medical settings. Nature Publishing Group UK 2021-03-16 /pmc/articles/PMC7966744/ /pubmed/33727616 http://dx.doi.org/10.1038/s41598-021-85389-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cohen, Isaac V. Makunts, Tigran Abagyan, Ruben Thomas, Kelan Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database |
title | Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database |
title_full | Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database |
title_fullStr | Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database |
title_full_unstemmed | Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database |
title_short | Concomitant drugs associated with increased mortality for MDMA users reported in a drug safety surveillance database |
title_sort | concomitant drugs associated with increased mortality for mdma users reported in a drug safety surveillance database |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966744/ https://www.ncbi.nlm.nih.gov/pubmed/33727616 http://dx.doi.org/10.1038/s41598-021-85389-x |
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