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

IF 10 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL EClinicalMedicine Pub Date : 2019-10-25 eCollection Date: 2019-12-01 DOI:10.1016/j.eclinm.2019.10.001
Sarah Watson, Ola Caster, Paula A Rochon, Hester den Ruijter
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引用次数: 104

Abstract

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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报告的女性和男性药物不良反应:半个世纪以来全球收集的个案报告汇总证据。
背景:药物不良反应(adr)是导致发病率和死亡率的重要原因。全国各地都有关于男女报告模式差异的报告。本研究的目的是评估全球范围内女性和男性药品上市后自发性ADR报告差异的证据。方法:我们分析了1967年至2018年1月2日期间世卫组织全球个案安全报告数据库VigiBase中收集的数据。VigiBase包含来自世卫组织国际药物监测规划131个成员国的1800多万份报告。结果:在有性别信息的报告中,9,056,566份(60.1%)涉及女性,6,012,804份(39.9%)涉及男性儿童和成人。在世界所有区域和所有类型的记者提交的女性不良反应报告都有所增加。在12-17岁及以上的所有年龄组中,女性报告的比例都较高。最大的差异是在18-44岁年龄组,不能用激素避孕药的使用来解释。严重和致命报告的比例在男性报告中更高。解释:全球自发报告的销售后监测数据表明,女性,从青春期开始,特别是在生育年龄,报告的不良反应比男性多。然而,在男性报告中,严重和致命的adr比例更高。我们的研究结果表明,在不良反应中存在重要的潜在性别差异。这些发现强调了在药物开发和监测的整个生命周期中考虑性别的重要性,并了解报告不良反应的潜在原因。
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来源期刊
EClinicalMedicine
EClinicalMedicine Medicine-Medicine (all)
CiteScore
18.90
自引率
1.30%
发文量
506
审稿时长
22 days
期刊介绍: eClinicalMedicine is a gold open-access clinical journal designed to support frontline health professionals in addressing the complex and rapid health transitions affecting societies globally. The journal aims to assist practitioners in overcoming healthcare challenges across diverse communities, spanning diagnosis, treatment, prevention, and health promotion. Integrating disciplines from various specialties and life stages, it seeks to enhance health systems as fundamental institutions within societies. With a forward-thinking approach, eClinicalMedicine aims to redefine the future of healthcare.
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