使用FDA不良事件报告系统 (FAERS) 对与vibegron相关的不良事件的不成比例分析:真实世界的药监测研究
Bangbei Wan1,2, Zhi Zhou3, Ning Ma3
1Reproductive Medical Center, Hainan Women and Children's Medical Center, Haikou, China. 939313612@qq.com.
European journal of medical research
|February 27, 2025
概括
维贝格龙是一种治疗过度活动膀 (OAB) 的药物,具有显著的安全性. 这项对不良事件报告的分析确定了特定的风险,特别是在女性和老年人身上,强调了仔细的监测.
科学领域:
- 药监和药物安全性分析.
- 对过度活跃的膀治疗药物的临床研究.
背景情况:
- 过度活性膀 (OAB) 综合征显著影响患者的生活质量.
- 维贝格龙为管理OAB症状提供了一种治疗选择.
研究的目的:
- 为了评估vibegron的安全概况.
- 使用来自FAERS数据库的不良事件 (AE) 报告的不成比例分析.
主要方法:
- 从2021年1月到2023年9月的FAERS数据的回顾性分析.
- 在数据清理后,确定了1137个与vibegron相关的AE报告.
- 分析了人口统计特征,临床数据,并在系统器官类 (SOC) 层面进行信号检测.
主要成果:
- 女性 (67.72%) 和老年人 (年龄大于64岁,15.84%) 占AE报告的比例更高.
- 在和尿路疾病 (ROR=7.72),胃肠道疾病 (ROR=1.38) 和呼吸系统疾病 (ROR=1.21) 中检测到显著的安全信号.
- 意外的副作用包括口腔干燥,发热,便秘和血压升高.
结论:
- 维贝格朗的安全性概况包括预期和意外的不良事件.
- 强调需要仔细选择和监测患者,特别是女性和老年人.
- 建议进行持续的药物监测和进一步的研究,以确保使用vibegron的安全有效的OAB治疗.
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