摘要
目的为药物利用评价和合理用药提供参考。方法对药学科学数据中心收录的5366例药品不良反应数据进行分类统计,重点分析特殊人群的用药结果、严重不良反应和可能出现的新的药品不良反应。结果与结论加强对特殊人群的用药监测,对于不良反应发生率较高的重点药品、容易出现严重不良反应以及可能出现新的不良反应的药品应当特别关注,及时发出药物安全警示。
Objective The references were provided for drug utilization review and rational drug use.Methods Classified statistic on 5366 cases of ADR in the Pharmaceutical Information Center was done,especially the ADR in special populations,serious ADR and new ADR dubiously.Results and Conclusion To strengthen the drug use monitoring of focus groups and key drugs,the higher incidences of ADR,especially serious adverse reaction cases and new adverse reaction cases should be needed to make a timely alert.
出处
《中国药事》
CAS
2011年第5期456-459,共4页
Chinese Pharmaceutical Affairs
