摘要
目的:提高药品不良反应监测工作社会效能,保障民众安全、合理用药。方法:采用文献研究、对比分析、数据归纳等方法,探讨我国药品不良反应监测体系现状与药品不良反应监测实施中面临的问题。结果与结论:当前我国药品不良反应监测存在着法规体系不健全、监测技术力量薄弱、广大医药人员认知度低等问题。需进一步强化宣传,加强监管,深入开发监测技术体系以及建立专家库和培训专业人才。
OBJECTIVE： To promote the development of clinical pharmacy and improve the social efficacy of ADR monitoring so as to ensure safe and rational use of drugs, METHODS：The current status of Chinese ADR monitoring system and the problems faced in the development of ADR monitoring were analyzed by means of literature review, contrasting analysis, and data reduction etc.RESULTS ＆ CONCLUSION： There are many problems existed in the current ADR monitoring, for instance： the regulations system of ADR monitoring is unsound, the monitoring technology is weak; the cognition level of many medical workers is still very low etc. It is urgently needed to intensify propaganda on ADR monitoring,strengthen ADR monitoring, develop technological system of monitoring,set up expert database and train professional talents.
出处
《中国药房》
CAS
CSCD
北大核心
2007年第29期2297-2301,共5页
China Pharmacy
关键词
药品不良反应
报告
监测监管
应用探讨
ADR
Reporting
Monitoring and supervision
Analysis of application
