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作 者:施湘萍 Shi Xiangping(Department of Medicine,Yangtze River Shipping General Hospital/Wuhan Brain Hospital,Wuhan 430015,China)
机构地区:[1]长江航运总医院/武汉脑科医院药学科,武汉430015
出 处:《中国药师》2020年第2期330-333,共4页China Pharmacist
摘 要:目的:分析不同药品生产企业生产的同一通用名药品说明书的内容差异,为临床合理用药提供有益参考。方法:收集我院在用的不同企业生产的相同通用名的药品说明书,比较分析其适应证、用法用量、禁忌证、不良反应、注意事项以及储存条件等内容的差异。结果:通过对比几组中、西药说明书中适应证、禁忌证、不良反应、注意事项、特殊人群用药、储存条件等方面的内容发现存在不同的缺项和差异。结论:药监部门、药品生产企业以及医疗机构应共同加强药品说明书规范化的管理。Objective:To analyze the differences in drug instructions of the medicines with the same generic names produced by different manufacturers,so as to provide references for medical institutions to use drugs rationally.Methods:The drug instructions from different manufacturers in our hospital were collected and their content differences and possible drug risks were analyzed.Results:Through the comparisons of indications,contraindications,adverse reactions,precautions,medication for special population,storage conditions and the other aspects in several groups of Chinese and western medicine instructions,there were various deficiencies and differences.Conclusion:Drug supervision departments,drug manufacturers and medical institutions should jointly strengthen the standardized management of drug instructions.
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