摘要
目的为临床安全合理用药提供参考。方法采用回顾性研究方法,探讨镇江市2005年至2015年国家药品不良反应监测系统药品不良反应(ADR)报告数据库中排名前5位的高危药品不良反应/不良事件(ADR/ADE)报告的一般规律及特点。结果与结论临床使用相关高危药品时,一定要合理规范用药,注意其ADR/ADE的临床表现,谨慎联合用药。
Objective To provide reference for clinical rational drug use and safety. Methods The method of retrospective study was used on the ADR reports through the national adverse drug reaction monitoring system of Zhenjiang city from 2005 to 2015, to compre- hensive analyze the rules and characteristics of the top 5 high- risk drug ADR/ADE reports. Results and Conclusion Clinical use of related high- risk drug must be in accordance with reasonable standard. We should pay attention to its clinical manifestation of ADR/ADE and be careful in drug combination.
出处
《中国药业》
CAS
2016年第19期64-66,共3页
China Pharmaceuticals
