药物回忆的持续挑战:来自FDA十年数据分析的见解
Seppe Ghijs1, Evelien Wynendaele1, Bart De Spiegeleer1
1Drug Quality and Registration (DruQuaR) group, Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, Ghent 9000, Belgium.
Journal of pharmaceutical and biomedical analysis
|July 19, 2024
概括
药物召回每年都在增加,杂质和污染物是主要原因. 持续评估旨在提高药物安全性并减少召回影响.
科学领域:
- 制药科学 制药科学
- 监管事务 监管事务
- 公共卫生 公共卫生
背景情况:
- 药品召回对患者安全和医疗保健系统构成重大风险.
- 了解召回趋势对于有效的监管监督至关重要.
研究的目的:
- 分析2012年至2023年间美国食品和药物管理局 (FDA) 的药物召回数据.
- 为了确定年度召回数量的趋势,原因,持续时间和受影响的产品单位.
- 评估与严重健康风险相关的召回比例.
主要方法:
- 对2012-2023年FDA药物召回数据的回顾性分析.
- 对召回频率,持续时间和规模的定量评估.
- 根据确定的原因和严重程度对召回进行分类.
主要成果:
- 平均每年开始召回330种药物,并观察到日益增长的趋势.
- 污染物/污染物 (37%) 是主要的召回原因,其次是控制 (28%) 和标签/包装问题 (19%).
- 召回的平均持续时间为1.3年,涉及约40万台,14%是I类 (严重的健康风险).
结论:
- 药品召回日益令人担忧,需要持续监测和分析.
- 解决杂质和控制问题等根本原因对于提高药物安全至关重要.
- 积极评估召回可以减轻医疗保健系统的影响,提高药物安全.
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