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1)  bad kickback of using medicine
用药不良反应
2)  adverse drug reactions
药品不良反应
1.
Discussion on the pharmaceautical enterprise′s responsibility for adverse drug reactions monitoring;
制药企业在药品不良反应监测工作中承担职责的探讨
2.
Analysis of 1549 cases of adverse drug reactions in Hefei;
合肥市1549份药品不良反应病例报告评析
3.
Analysis of 258 cases of adverse drug reactions;
258例药品不良反应报告分析
3)  Adverse reaction
药物不良反应
1.
Medicine prevents and cures diseases,but on the other hand,it also exerts the unexpected effect which is harmful to organism at the same time,and this is called adverse reaction.
药物在防治疾病的同时也会产生对机体有害的作用和不期望产生的作用,即药物不良反应。
2.
Objective To observe the adverse reaction incurred from lower heart rate by large dose metoprolol in the elderly patients with unstable angina pectoris( UAP).
目的探讨较大剂量美托洛尔(抗心绞痛药)治疗老年不稳定心绞痛 (UAP)心率减低时,可能出现的药物不良反应。
4)  ADR
药品不良反应
1.
Retrospective Analysis of New and Severe ADR Case Reports in Our Hospital from 2002 to 2006;
我院2002~2006年新的和严重的药品不良反应报告分析
2.
Predisposing Factors of ADR:Analysis of 101 Cases;
我院101例药品不良反应报告分析
3.
Analysis of 88 Case Reports of ADRs From Our Hospital;
我院88例药品不良反应报告分析
5)  Adverse drug reaction
药物不良反应
1.
The practice and experience of adverse drug reaction nursing emergency procedure;
实施药物不良反应监测护理应急流程的做法与体会
2.
Causality assessment of signal adverse drug reaction;
单一事件药物不良反应的因果关系评价
3.
Analysis of 110 incidences of adverse drug reactions;
110例药物不良反应报告分析
6)  adverse drug reaction(ADR)
药品不良反应
1.
Objective By analyzing the children s serious adverse drug reaction(ADR) reports of Guangdong Province in 2006, to provide references for administration and ensure safety use of drug in pediatric clinic.
目的统计分析广东省2006年儿童严重药品不良反应报告数据,为确保儿科临床安全、合理用药,减少或避免儿童严重药品不良反应发生提供参考。
2.
OBJECTIVE To comparative analyses the characteristics and the related factors of adverse drug reaction(ADR) occurred in our hospital during the period of 2005~2006,and provide reference for clinical administration.
目的比较分析2005~2006年我院药品不良反应(ADR)发生特点及相关因素,为临床合理用药提供参考。
3.
By discussing the function of municipal monitoring organization in the evaluation system of adverse drug reaction(ADR),to promote the feedback of ADR monitoring information and strengthen the training of ADR monitoring knowledge,guide reporting units pay more attention to the new and serious ADR,so as to explore the model for analysis and appraisal of ADR cases and information feedback.
通过分析地市级监测机构在药品不良反应监测体系中发挥的独特作用,提出地市级监测机构应反馈监测信息;加强宣传、培训;引导报告单位多关注新的、严重的不良反应;探索开展病例报告分析、评价和反馈工作的有效工作模式。
补充资料:不良反应
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性质:不符合用药目的,引起病人生理生化机能紊乱或形态学变化,不利于患病的机体,甚至给病人带来痛苦的药物反应统称为不良反应。包括副作用、毒性反应、后遗效应和变态反应。

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