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Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century

BACKGROUND: Adverse drug reactions (ADRs) are an important cause of morbidity and mortality. Reports on differences in reporting patterns between women and men exist nationally. The goal of the present study was to assess the global evidence on spontaneous post-marketing ADR reporting differences be...

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Autores principales: Watson, Sarah, Caster, Ola, Rochon, Paula A, den Ruijter, Hester
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933269/
https://www.ncbi.nlm.nih.gov/pubmed/31891132
http://dx.doi.org/10.1016/j.eclinm.2019.10.001
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author Watson, Sarah
Caster, Ola
Rochon, Paula A
den Ruijter, Hester
author_facet Watson, Sarah
Caster, Ola
Rochon, Paula A
den Ruijter, Hester
author_sort Watson, Sarah
collection PubMed
description BACKGROUND: Adverse drug reactions (ADRs) are an important cause of morbidity and mortality. Reports on differences in reporting patterns between women and men exist nationally. The goal of the present study was to assess the global evidence on spontaneous post-marketing ADR reporting differences between reports for women and men. METHODS: We analysed data collected within VigiBase, the WHO global database of individual case safety reports, between 1967-2 January 2018. VigiBase contains more than 18 million reports from the 131 member countries of the WHO Programme for International Drug Monitoring. FINDINGS: Of the reports with information on sex, 9,056,566 (60.1%) concerned female and 6,012,804 (39.9%) male children and adults. More female ADR reports were submitted in all regions of the world and by all types of reporters. A higher proportion of female reports was seen in all age groups from the age group 12-17 years and older. The largest difference was observed in the age group of 18–44 years and could not be explained by hormonal contraceptive use. The proportion of serious and fatal reports was higher for male reports. INTERPRETATION: Global post marketing surveillance data on spontaneous reports indicate that women, from puberty and onwards and especially in their reproductive years, report more ADRs than men. However, there is a higher proportion of serious and fatal ADRs among male reports. Our results suggest important underlying sex-related differences in ADRs. These findings highlight the importance of considering sex throughout the entire life-cycle of drug development and surveillance and understanding the underlying reasons for reporting ADRs.
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spelling pubmed-69332692019-12-30 Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century Watson, Sarah Caster, Ola Rochon, Paula A den Ruijter, Hester EClinicalMedicine Research Paper BACKGROUND: Adverse drug reactions (ADRs) are an important cause of morbidity and mortality. Reports on differences in reporting patterns between women and men exist nationally. The goal of the present study was to assess the global evidence on spontaneous post-marketing ADR reporting differences between reports for women and men. METHODS: We analysed data collected within VigiBase, the WHO global database of individual case safety reports, between 1967-2 January 2018. VigiBase contains more than 18 million reports from the 131 member countries of the WHO Programme for International Drug Monitoring. FINDINGS: Of the reports with information on sex, 9,056,566 (60.1%) concerned female and 6,012,804 (39.9%) male children and adults. More female ADR reports were submitted in all regions of the world and by all types of reporters. A higher proportion of female reports was seen in all age groups from the age group 12-17 years and older. The largest difference was observed in the age group of 18–44 years and could not be explained by hormonal contraceptive use. The proportion of serious and fatal reports was higher for male reports. INTERPRETATION: Global post marketing surveillance data on spontaneous reports indicate that women, from puberty and onwards and especially in their reproductive years, report more ADRs than men. However, there is a higher proportion of serious and fatal ADRs among male reports. Our results suggest important underlying sex-related differences in ADRs. These findings highlight the importance of considering sex throughout the entire life-cycle of drug development and surveillance and understanding the underlying reasons for reporting ADRs. Elsevier 2019-10-25 /pmc/articles/PMC6933269/ /pubmed/31891132 http://dx.doi.org/10.1016/j.eclinm.2019.10.001 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Watson, Sarah
Caster, Ola
Rochon, Paula A
den Ruijter, Hester
Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century
title Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century
title_full Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century
title_fullStr Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century
title_full_unstemmed Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century
title_short Reported adverse drug reactions in women and men: Aggregated evidence from globally collected individual case reports during half a century
title_sort reported adverse drug reactions in women and men: aggregated evidence from globally collected individual case reports during half a century
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933269/
https://www.ncbi.nlm.nih.gov/pubmed/31891132
http://dx.doi.org/10.1016/j.eclinm.2019.10.001
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