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Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase
Cannabidiol is the first cannabis-derived drug approved for the treatment of Lennox–Gastaut syndrome, Dravet syndrome, and Tuberous Sclerosis Complex. In the current study, we performed a descriptive analysis followed by a disproportionality analysis of potential adverse events caused by CBD extract...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610535/ https://www.ncbi.nlm.nih.gov/pubmed/37895891 http://dx.doi.org/10.3390/ph16101420 |
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author | Calapai, Fabrizio Mannucci, Carmen McQuain, Liana Salvo, Francesco |
author_facet | Calapai, Fabrizio Mannucci, Carmen McQuain, Liana Salvo, Francesco |
author_sort | Calapai, Fabrizio |
collection | PubMed |
description | Cannabidiol is the first cannabis-derived drug approved for the treatment of Lennox–Gastaut syndrome, Dravet syndrome, and Tuberous Sclerosis Complex. In the current study, we performed a descriptive analysis followed by a disproportionality analysis of potential adverse events caused by CBD extracted from the VigiBase(®) database. Furthermore, the biological plausibility of the association between CBD and the serotonin 5-HT(1A) receptor as a possible cause of adverse events was analyzed and discussed. Data were extracted from the VigiBase(®) database using the VigiLyze(®) signal detection and signal management tool. Adverse events in VigiBase(®) reports were coded using MedDRA, version 19 of Preferred Terms (PTs). Data were uploaded into SPSS software and analyzed via a disproportionality analysis. Statistically significant disproportionality signals for CBD were found for “weight decreased” (5.19 (95% CI: 4.54–5.70)), “hypophagia” (3.68 (95% CI: 3.22–5.27)), and “insomnia” (1.6 (95% CI: 1.40–1.83)). Positive IC025 values were found for “weight decreased” (2.2), “hypophagia” (1.3), and “insomnia” (0.5), indicating a surplus of reported cases. CBD’s interactions with 5-HT(1A) serotonin receptors may offer a potential biological explanation for the occurrence of insomnia in patients. It is noteworthy that the risk profiles mentioned in the information for prescribing CBD as an antiepileptic agent by regulatory agencies showed disparities specifically related to the adverse event “insomnia”. |
format | Online Article Text |
id | pubmed-10610535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106105352023-10-28 Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase Calapai, Fabrizio Mannucci, Carmen McQuain, Liana Salvo, Francesco Pharmaceuticals (Basel) Article Cannabidiol is the first cannabis-derived drug approved for the treatment of Lennox–Gastaut syndrome, Dravet syndrome, and Tuberous Sclerosis Complex. In the current study, we performed a descriptive analysis followed by a disproportionality analysis of potential adverse events caused by CBD extracted from the VigiBase(®) database. Furthermore, the biological plausibility of the association between CBD and the serotonin 5-HT(1A) receptor as a possible cause of adverse events was analyzed and discussed. Data were extracted from the VigiBase(®) database using the VigiLyze(®) signal detection and signal management tool. Adverse events in VigiBase(®) reports were coded using MedDRA, version 19 of Preferred Terms (PTs). Data were uploaded into SPSS software and analyzed via a disproportionality analysis. Statistically significant disproportionality signals for CBD were found for “weight decreased” (5.19 (95% CI: 4.54–5.70)), “hypophagia” (3.68 (95% CI: 3.22–5.27)), and “insomnia” (1.6 (95% CI: 1.40–1.83)). Positive IC025 values were found for “weight decreased” (2.2), “hypophagia” (1.3), and “insomnia” (0.5), indicating a surplus of reported cases. CBD’s interactions with 5-HT(1A) serotonin receptors may offer a potential biological explanation for the occurrence of insomnia in patients. It is noteworthy that the risk profiles mentioned in the information for prescribing CBD as an antiepileptic agent by regulatory agencies showed disparities specifically related to the adverse event “insomnia”. MDPI 2023-10-05 /pmc/articles/PMC10610535/ /pubmed/37895891 http://dx.doi.org/10.3390/ph16101420 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Calapai, Fabrizio Mannucci, Carmen McQuain, Liana Salvo, Francesco Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase |
title | Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase |
title_full | Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase |
title_fullStr | Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase |
title_full_unstemmed | Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase |
title_short | Pharmacological Evaluation of Signals of Disproportionality Reporting Related to Adverse Reactions to Antiepileptic Cannabidiol in VigiBase |
title_sort | pharmacological evaluation of signals of disproportionality reporting related to adverse reactions to antiepileptic cannabidiol in vigibase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610535/ https://www.ncbi.nlm.nih.gov/pubmed/37895891 http://dx.doi.org/10.3390/ph16101420 |
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