更大的问题是，受问题支配的FDA的不良反应事件报告系统不能系统的衡量药品引起的真实副作用的多少。
The bigger issue is that the FDA's problem-ridden Adverse Event Reporting System isn't a systematic measure of how often drugs really cause side effects.
处方事件监测用非干预性、观察性药品不良反应监测方法，1981年在英国最早开展。
Prescription Event monitoring (PEM) is a non-interventional observational method of adverse drug reaction monitoring, which was established first in England in 1981.
阐述自2009年药品不良反应的主要事件以及预防事故发生的安全措施和程序。
It will elaborate the main issues from ADR 2009 as well as safety measures and procedures in case of accidents.
目的：正确区分药品不良反应(adr)及与药品相关的药害事件。
OBJECTIVE: To differentiate and analyze adverse drug reactions (ADR) and drug misadventures.
结论临床医务工作者需重视退药现象和药品不良反应，通过加强干预措施可明显减少退药事件的发生。
Conclusion great importance should be attached to adverse drug reaction, the incidence of drug repercussion can be greatly reduced by talking intervention measures.
结论临床医务工作者需重视退药现象和药品不良反应，通过加强干预措施可明显减少退药事件的发生。
Conclusion great importance should be attached to adverse drug reaction, the incidence of drug repercussion can be greatly reduced by talking intervention measures.
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