摘要
目的为提高药品不良反应报告的质量提供参考意见。方法评价淮北市2006年、2007年收集的《药品不良反应/事件报告表》质量情况,针对存在的问题,提出解决办法。结果与结论我国的药品不良反应监测体系正逐渐由报告体系向评价体系过渡。提高药品不良反应报告的质量,将是保证其顺利过渡的关键。
Objective To evaluate the quality of the "Adverse Drug Reaction/Incident Report Table" of Huaibei in 2006 and 2007. Methods To analyze the " Adverse Drug Reaction/Incident Report Table" of Huaibei in 2006 and 2007 in order to find out problems and improve the quality of the reports. Results and Conclusions To raise the quality of the report of ADRs, and to provide a scientific basis for the ADR monitoring.
出处
《中国药事》
CAS
2009年第2期157-158,共2页
Chinese Pharmaceutical Affairs