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多内的全面安全评估:基于FDA不良事件报告系统的药监测分析
Shuo Li1, Wenlong Qian1, Zhuo Zhang1
1Department of Neurology, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, Anhui, China.
Frontiers in neurology
|December 26, 2025
概括
这项研究分析了多尼佩西尔的不良事件,揭示了恶心和吐等常见副作用,以及严重的风险,如跌倒和低血压,特别是在女性中. 仔细监测和个性化治疗对于阿尔茨海默病患者至关重要.
科学领域:
- 药物监督 药物监督 药物监督
- 神经科学是一个神经科学.
- 老年学是一门学科.
背景情况:
- 阿尔茨海默氏症 (AD) 是一个日益严重的全球健康挑战.
- 多尼尼西尔是一种常见的AD治疗方法,但面临安全问题.
- 迫切需要评估donepezil的现实世界不良事件概况.
研究的目的:
- 综合评估donepezil的安全性和不良事件概况.
- 通过使用现实世界的数据来识别与多尼佩西尔治疗相关的潜在风险.
主要方法:
- 对多内的不良事件报告从FAERS数据库 (2004年第一季度 - 2024年第四季度) 中提取.
- 使用ROR,PRR,BCPNN和MGPS进行了不成比例的分析.
- 分析了26,120例使用多尼佩西尔作为第一个可疑剂的不良药物反应 (ADR).
主要成果:
- 常见的不良事件包括恶心,吐,昏迷和头.
- 检测到的显著的意外副作用包括跌倒,低血压,震,认知障碍,躁狂和胸腔炎.
- 副作用在女性中更为频繁 (51.3%),并且发生在治疗开始后30天内 (41%).
结论:
- 多尼西尔治疗需要专注于心血管和神经系统不良事件.
- 建议女性,老年人和患有并发症的患者特别小心.
- 建议加强心脏监测,剂量调整,并探索个性化治疗方案,以提高长期的安全性.
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