目的：为进一步规范我国药品说明书提供参考。方法将日常工作中发现的药品说明书在内容完整性、可读性和及时性方面存在的问题进行归纳整理。结果和结论完善药品说明书需要药品监管部门、生产企业、药品使用单位共同关注。“,”Objective To provide reference for further standardizing Drug instructions in China. Methods We summarised the problems of integrity, readability and timeliness in the content of the Drug instructions which were found in daily work. Results and Conclusion The improvement of drug instructions needed the common attention of drug regulatory agency, manufacturers and department related to drug use.