摘要
目的为保障药品质量和加强药品养护工作提供参考。方法将门诊药房所有药品说明书中贮藏项内容进行分类统计,并评价考察结果。结果所调查的1 029种药品中,西药740种,中成药238种,生物制品51种;药品贮藏项下47.42%(488/1 029)有光线要求,79.20%(815/1 029)有密封要求,51.31%(528/1 029)有温度要求。结论应重视药品的贮藏与养护,规范药品说明书贮藏项表述,以保障临床用药安全、有效。
Objective To provide reference for ensuring the drug quality and drug storage. Methods The storage item content of all drug instructions in the outpatient pharmacy were performed the classified statistical analysis. The inspection results were evaluat- ed. Results The 1 029 kinds of drug were instigated, in which 740 kinds were Western medicine,238 kinds were Chinese patent medicine, and 51 kinds were biological product; in the storage item of the drug instructions, the light requirements accounted for 47.42% (488/1 029),the sealing requirements accounted for 79.20% (815/1 029) and the temperature requirements accounted for 51.31% (528/1 029). Conclusion It is necessary to pay attention to the storage and conservation of drugs and standardize the state- ment of storage item in drug instructions, in order to guarantee the safety and efficiency of medication in clinic.
出处
《中国药业》
CAS
2014年第18期16-18,共3页
China Pharmaceuticals
关键词
药品说明书
贮藏管理
风险分析
风险评价
drug instructions
storage management
risks analysis
risks evaluation