1) adverse drug events
药品不良事件
1.
Adverse drug events:analysis of 387 cases
387例药品不良事件报告分析
2.
This paper discussed the contributing factors and responsibilities of the various departments for adverse drug events,and established a quantitative relation between the contributing factors and responsibilities.
本文运用系统科学的思想,论述了药品不良事件的成因以及不同部门和人群的责任,并建立了药品不良事件的成因与责任之间的定量化关系。
2) Adverse Drug Event
药品不良事件
1.
In the process of dealing with the adverse drug event,the key points are open and transparent process,full information provided and scientific and strict procedures.
通过对TGN1412不良事件及其发生后各方反应的回溯性分析,探讨监管部门、媒体、专家和企业对药品不良事件的反应模式及其应对模式的效率与效果。
3) adverse drug reaction/event
药品不良反应/事件
1.
Objective To investigate the features of the severe adverse drug reaction/event(ADR/ADE).
目的了解严重药品不良反应/事件发生情况及特点。
4) adverse drug reaction/event(ADR/ADE)
药品不良反应/事件
1.
Objective To investigate the epidemiological characteristics of the adverse drug reaction/event(ADR/ADE) induced by anticancer drugs.
方法采用回顾性研究方法,对江苏省2003年12月至2008年2月收集的1956例抗肿瘤药品不良反应/事件病例报告进行综合分析。
5) Adverse drug events
药物不良事件
1.
Adverse drug events of the clinical analysis and prevention of;
药物不良事件的临床分析及预防探讨
2.
Objective:To assess existence and preventability of adverse drug events(ADEs) and to investigate excess length of stay and extra hospital charges of the ADEs.
目的:调查住院病人药物不良事件(ADE)发生率、因ADE而造成的医疗费用、延长的住院时间及ADE的可防范率。
3.
The collection of adverse drug events(ADE) represents one of the inherent attributes of qualified(approved) drugs.
药物不良事件(adverse drug events,ADE)为合格药品的固有属性之一。
6) adverse drug event
药物不良事件
1.
Objective To investigate the basic principles and important rules of forensic identification of adverse drug events and to accumulate basic data and to provide references for forensic identification of similar cases.
目的研究药物不良事件的法医学鉴定原则及注意事项,为此类案件的法医学鉴定提供参考并积累基础资料。
补充资料：非法提供麻醉药品、精神药品罪
非法提供麻醉药品、精神药品罪：指依法从事生产、运输、管理、使用国家管制的麻醉药品、精神药品的单位和个人，明知他人是吸毒者，而向其提供国家管制的能够使人成瘾的麻醉药品、精神药品的行为。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条