摘要
2019年8月修订《药品管理法》增加医疗机构应当遵循药品临床应用指导原则、临床诊疗指南和药品说明书等合理用药,明确了药品说明书在临床用药法律定位。临床医师通常忽视药品说明书中用法用量、注意事项等技术内容导致患者损害引发医疗纠纷。医师应当习惯开具处方或医嘱前了解或阅读药品说明书习惯,减少不合理用药造成患者损害。
The Drug Administration Law was revised in August 2019 added that medical institutions should follow the guiding principles for clinical application of drugs,clinical diagnosis and treatment guidelines,drug instructions,and clarified the legal positioning of drug instructions in clinical medication.Clinicians usually ignore the technical contents such as usage and dosage,precautions and so on in the drug instructions,causing patient damage and causing medical disputes.Doctors should get used to the habit of knowing or reading drug instructions before issuing prescriptions or doctor’s orders,so as to reduce the damage to patients caused by irrational drug use.
作者
刘亮
范贞
LIU Liang;FAN Zhen(Third Medical Center,The General Hospital of People’s Liberation Army,Beijing 100039;Beijing Bairui Law Firm,Beijing 100097)
出处
《中国临床药理学杂志》
CAS
CSCD
北大核心
2020年第4期456-457,461,共3页
The Chinese Journal of Clinical Pharmacology
基金
北京市社会科学基金资助项目(15JGB121).
关键词
药品说明书
药品管理法
医疗纠纷
drug instructions
drug administration law
medical disputes