目的:分析药剂科在药品不良反应方面的检测管理工作中的问题,并作出应对这些问题的对策。方法:通过针对药剂科多年来的药品不良反应报告,以及相应的检测管理工作分析来进行探讨。结果与结论:只有加强规章制度的规范化操作,树立正确的认知体系,增强药品安全责任体现的建设,才能够完善这方面的检测管理。 OBJECTIVE: To analyze the problems in the management of pharmaceuticals in adverse drug reactions and to make countermeasures against these problems. Methods: Through years of drug adverse reactions reports, as well as the corresponding test management analysis to investigate. RESULTS AND CONCLUSION: Only by strengthening the standardization of rules and regulations, establishing the correct cognition system and enhancing the construction of drug safety responsibility can we improve the testing and management in this aspect.