中国药物警戒 ›› 2025, Vol. 22 ›› Issue (2): 188-192.
DOI: 10.19803/j.1672-8629.20240621

• 法规与管理研究 • 上一篇    下一篇

已上市中成药说明书安全信息修订实践与思考

朱兰1, 邵波1, 朱彦2, 戴洁3, 钟诗琦4   

  1. 1国家药品监督管理局药品评价中心,国家药品监督管理局药物警戒研究与评价重点实验室,北京 100076;
    2中国中医科学院中医药信息研究所,北京 100700;
    3陕西省药品不良反应监测中心,陕西 西安 710065;
    4贵州省药品评价中心,贵州 贵阳 550081
  • 收稿日期:2024-08-19 出版日期:2025-02-17 发布日期:2025-02-17
  • 作者简介:朱兰,女,硕士,副主任药师,药品不良反应监测与评价。
  • 基金资助:
    国家自然科学基金资助项目(82174534); 中央级公益性科研院所基本科研业务费专项资金资助:中医药语义信息标准化探索研究(ZZ13-YQ-126)

Current Progress and Considerations in Updating the Safety Information in Labels of Chinese Traditional Patent Medicines

ZHU Lan1, SHAO Bo1, ZHU Yan2, DAI Jie3, ZHONG Shiqi4   

  1. 1Center for Drug Reevaluation, NMPA/ NMPA Key Laboratory for Research and Evaluation of Pharmacovigilance, Beijing 100076, China;
    2Institute of Information on Traditional Chinese Medicine, CACMS, Beijing 100700, China;
    3Shaanxi Center for ADR Monitoring, Xi'an Shaanxi 710065, China;
    4Center for Drug Reevaluation, Guiyang Guizhou 550081, China
  • Received:2024-08-19 Online:2025-02-17 Published:2025-02-17

摘要: 目的 总结已上市中成药说明书安全信息修订相关工作经验。方法 梳理已上市中成药说明书【不良反应】【禁忌】【注意事项】和“警示语”修订相关指导原则及要求,结合实际工作提出针对性建议。结果 由于历史原因,部分已上市中成药说明书存在安全信息缺失的情形,应该及时予以修订,使医务人员、患者及时全面了解药品安全信息,从而指导临床安全合理用药。结论 说明书修订是药品风险管理措施之一,解决了说明书安全信息缺失的问题后,仍然需要持续开展不良反应监测、上市后研究与评价发现药品风险,通过修订说明书等措施控制药品风险。

关键词: 中药, 说明书, 安全性信息, 药品不良反应, 禁忌, 注意事项

Abstract: Objective To review Current status of updating safety information in labels of Chinese traditional patent medicines. Methods To analyze the guidelines and requirements for the updating of information on adverse reactions, contraindications, precautions and warnings information in the labels of Chinese traditional patent medicines, and to make suggestions based on working experience. Results For some historical reasons, safety information is missing from some Chinese traditional patent medicine labels and should be added to provide guidance to healthcare professionals and patients on the use of medicines. Conclusion Revision of labeling and updating of safety information is one of the risk management measures, after solving the problem of missing safety information, there is still a need for continuous monitoring of adverse reactions, post-marketing research to identify drug risks, and to control the risks by revising labels and other measures.

Key words: Chinese Traditional Medicine, Labels, Safety Information, Adverse Drug Reaction, Contraindications, Precautions

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