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基于上市许可持有人的药品不良反应主动监测模式的构建与评估研究

Research on the Construction and Evaluation of Active Monitoring Model of Adverse Drug Reactions by Marketing Authorization Holder
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摘要 目的:探讨药品上市许可持有人(Marketing Authorization Holder,MAH)的药品不良反应主动监测创新模式的构建及其效果评估,为落实MAH药物警戒主体责任提供实证参考。方法:首先针对MAH药物警戒的现存挑战,基于中国医院药物警戒系统(Chinese Hospital Pharmacovigilance System,CHPS)设计MAH针对药品不良反应的主动监测模式,包括不良反应的监测、识别、评估及控制;再以注射用卡瑞利珠单抗为例分析主动监测效果。结果与结论:从MAH视角,构建基于CHPS整合循证证据和真实世界数据开展ADR主动监测的创新模式,包括运行模式、数据挖掘及模型构建。该主动监测模式被成功应用到以卡瑞利珠单抗为例的临床实践中,取到良好的效果。该研究成果不仅能帮助MAH开展药品监测工作,落实药品全生命周期主体责任,还能丰富药物警戒的内涵,为促进药物警戒发展和合理用药提供具有可操作性的实证参考。 Objective:To explore the construction and evaluation of active monitoring innovation model of adverse drug reactions by marketing authorization holder(MAH),to provide empirical reference for implementing the main responsibility of MAH pharmacovigilance.Methods:For the existing challenges of MAH pharmacovigilance,an active monitoring model for MAH adverse drug reactions was designed based on the Chinese Hospital Pharmacovigilance System(CHPS),including the monitoring,identification,evaluation and control of adverse reactions.Camrelizumab was used as an example to analyze the effectiveness of active monitoring.Results and Conclusion:From the perspective of MAH,this study design an innovation model for active monitoring of ADR based on CHPS integrating evidence-based evidence and real-world data,including operation mode,data mining and model design.This active monitoring model has been successfully applied in clinical practice represented by camrelizumab,and achieves good results.The research can not only help MAH to carry out drug monitoring work and implement the main responsibilities of the entire life cycle of drugs,but also enrich the connotation of pharmacovigilance and provide practical empirical reference for promoting the development of pharmacovigilance and rational drug use.
作者 陈子桃 赖云锋 陈新林 许星莹 张桂兰 徐梦丹 Chen Zitao;Lai Yunfeng;Chen Xinlin;Xu Xingying;Zhang Guilan;Xu Mengdan(Guangzhou University of Chinese Medicine,Guangzhou 510006,China;Guangdong Pharmaceutical University,Guangzhou 510006,China)
出处 《中国药事》 CAS 2024年第3期261-268,共8页 Chinese Pharmaceutical Affairs
基金 广东省药品监督管理局2022年科技创新项目(编号2022ZDZ06) 广东省中医药局项目(编号20204003) 广东省哲学社会科学规划项目(编号GD23SQGL01) 广东省教育科学规划课题(编号2022GXJK060) 广东省基础与应用基础研究基金项目(编号2022A1515220162) 广东省基础与应用基础研究基金项目(编号2022A1515220148)。
关键词 上市许可持有人 药品不良反应 主动监测 模式构建 中国医院药物警戒系统 marketing authorisation holder adverse drug reaction active monitoring model construction Chinese Hospital Pharmacovigilance System
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