EudraVigilance的见解:通过母乳养在婴儿中怀疑药物不良反应
Ida M Heerfordt1, Ditte Resendal Gotfredsen1,2, Henrik Horwitz1,2
1Department of Clinical Pharmacology, Copenhagen University Hospital - Bispebjerg and Frederiksberg, Copenhagen, Denmark.
British journal of clinical pharmacology
|April 7, 2025
概括
十年的数据揭示了922个怀疑的药物不良反应 (ADR) 在母乳养的婴儿. 尽管发生了严重事件和死亡事故,但报告率较低,这突出显示了母亲使用药物的药监监报告不足.
科学领域:
- 药物监督 药物监督 药物监督
- 儿科药理学 儿科药理学
- 药品安全 药品安全
背景情况:
- 在母乳养期间,母亲使用药物可能会通过母乳将婴儿暴露在药物中.
- 了解这些暴露的风险对于婴儿的健康和安全至关重要.
- 营销后监测系统对于监测这种脆弱人群的药物安全至关重要.
研究的目的:
- 描述通过母乳接触药物的婴儿怀疑的药物不良反应 (ADRs).
- 分析这些副作用的频率,严重程度和性质.
- 评估母乳养期间母亲服用药物的潜在风险.
主要方法:
- 从欧洲药物监督数据库 (EudraVigilance) 中分析了母乳养婴儿中疑似ADR报告.
- 包括2013年1月1日至2023年7月1日的数据.
- 根据婴儿人口统计,药物类型和严重程度对副作用的分类.
主要成果:
- 在母乳养的婴儿中报告了922个可疑的副作用.
- 133例 (14%) 是严重的,包括15例死亡,主要与甲和二甲有关.
- COVID-19疫苗占报告的52%,神经系统药物与最严重的副作用有关.
结论:
- 报告的副作用的数量很少,这表明,对于通过母乳传播的药物,在药监监中报告不足.
- 对于母乳养母亲和婴儿的营销后监测仍然存在挑战.
- 报告不足仍然是确保该人口中药物安全的关键问题.
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