通过使用不良事件自发报告数据库和处方索赔数据库来评估pregabalin诱导的胀
Hitoshi Ito1, Yoshitaka Hasegawa1, Mamoru Maeda1
1AIN Holdings Inc., Shibuya-ku, Tokyo 151-0053, Japan.
The International journal of pharmacy practice
|April 18, 2025
概括
普雷加巴林的使用与水有关,特别是在治疗的早期. 较高的初始剂量 (≥150 mg/天) 会增加日本患者的胀和循环利尿剂处方的风险.
科学领域:
- 药物监督 药物监督 药物监督
- 临床药理学 临床药理学
背景情况:
- 胀是普雷加巴林的潜在副作用,影响患者的生活质量.
- 同时服用利尿剂可能会加剧与相关的不良事件.
研究的目的:
- 为了调查使用普雷加巴林的日本患者的水和循环利尿剂处方的发生.
- 分析发作的时间特征和相关因素.
主要方法:
- 利用了日本不良药物事件报告和药房索赔数据库.
- 采用后勤回归和时间发病分析,用于结胀协会.
- 应用了处方序列对称性分析来评估循环利尿剂联合处方.
主要成果:
- 普雷加巴林对瘤显示出显著的调整报告几率比率 (6.89).
- 发作的中位时间为16.0天.
- 调整后的序列比值为1.17,表明与循环利尿剂的处方存在关联,特别是在每天150毫克或更高的初始剂量时.
结论:
- edem 和循环利尿剂的处方与pregabalin使用有关.
- 发作在普雷加巴林治疗的早期阶段更为频繁.
- 较高的普雷加巴林初始剂量 (≥150毫克/天) 与胀和利尿剂使用的风险增加有关.
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