对药品不良反应应及时向当地药品监督管理部门报告。
Drug adverse reactions shall be duly reported to the local drug administration authorities.
摘要：目的：为提高医务人员对药品不良反应(adr)的认知水平提供参考。
ABSTRACT: OBJECTIVE: To provide reference for improving the cognition of medical staff for adverse drug reactions (ADR).
山东省通过建立二级审核和评价员制度，加强对药品不良反应报告的质量控制。
Two-level audit and evaluation system established in Shandong Province have strengthened the quality control of ADR reports.
目的调查临床医师对药品不良反应(adr)纠纷的防范和应对情况，探索医疗机构防范和应对adr纠纷较为有效的方法。
Objective to investigate the prevention and response of clinicians to disputes of adverse drug reactions (ADR), and explore effective ways for medical institutions to deal with disputes of ADR.
目的了解医务人员对药品不良反应（ADR）监测相关知识的认识和掌握情况，为更好的开展ADR监测工作提供依据和参考。
Objective To conduct a survey about adverse drug reactions(ADR) knowledge among medical staff in our hospital as to improve and promote the reporting and monitoring of ADR.
即使卫生专业人员对所给药物和产生反应之间的确切关联存有不确定性，也应做出药品不良反应的报告。
Health professionals should report ADRs even if they are doubtful about the precise relationship between the given medicine and reaction.
对药物产生的非预期、有害反应(称作药品不良反应)位居许多国家主要死因之列。
Unintended, harmful reactions to medicines (known as adverse drug reactions) are among the leading causes of death in many countries.
目的对106例严重药品不良反应病例进行分析挖掘警戒信号，为临床安全合理用药提供警示。
The purpose of the 106 cases of serious cases of adverse drug reactions Analytical Mining warning signal, rational use of drugs for clinical safety to provide a warning.
方法：从法律内涵、监管部门、处理措施、法律责任等角度对假药与药品不良反应进行分析对比。
METHODS: To analyzed and the fake drug and adverse drug reactions from aspects of legal connotation, drug control institute, measures of management, legal responsibility etc.
全科医生行业报纸对423名医生所做的调查问卷中，有25%的医生表示曾经治疗过由于购买互联网上的药品而引起不良反应的病人。
The poll of 423 doctors for GP newspaper found 25% have treated patients for unwelcome reactions caused by medicines bought over the Internet.
结论：通过这种方法可以及时对病因假设进行初步验证，同时也为基于药品不良反应数据库开展相关研究提供了一种新思路。
Conclusion: in this way we can timely validate a pathogenic hypothesis and find a new way for developing the study that is based on the database.
方法：对我国当前医疗机构药品不良反应的现状进行分析。
METHODS:The current situation of monitoring and reporting system of ADR in medical organizations were analyzed.
目的对2005年江苏省药品不良反应自愿报告数据库进行信号检测。
Objective The Signal for Adverse Drug Reaction (ADR) spontaneous reporting database of Jiangsu Province in 2005 is detected.
方法：采用回顾性分析方法对2006 ~ 2007年泰安市药品不良反应监测中心收到的134例左氧氟沙星不良反应病例报告进行统计分析。
Methods: 134 ADR reports of Levofloxacin collected by Taian Center for ADR Monitoring from 2006 to2007were analyzed using retrospective study method.
目的探讨药品不良反应(adr)中相关责任方对最低伤害补偿级别的选择，并分析其特征。
Objective To investigate the selection of lowest grade of injury in compensation of adverse drug reactions (ADR) for responsible parties, and analyse the characteristics.
方法：对嘉兴市药品不良反应监测中心2007年收集的809例抗感染药不良反应报告进行回顾性分析。
Method: Retrospectively analysis of 809 ADRs cases due to anti-infective drugs were collected by ADR Monitoring Center of Jiaxing in 2007.
方法对124例药品不良反应(adr)报告进行分析。
METHODS 124 cases reports of Adverse Drug Reaction (ADR) were analyzed.
方法采用回顾性研究方法，对我院377例药品不良反应报告进行汇总分析。
Method We conducted a retrospective study to analyze 377 ADR reports in our hospital.
本文试对我国现行部门规章《药品不良反应报告和监测管理办法》中药品不良反应概念存在的问题进行探讨，提出修改建议。
This paper discussed problems in definition of ADR in regulation of Administrative Measures on Reporting and Monitoring of ADR, and put forward some proposals.
目的通过对506份药品不良反应报告的分析，提醒临床医务人员加强药品安全意识，减少药品不良反应的发生。
Objective to analyse the adverse drug reaction reports, so as to promote rational drug use in the clinic.
第八十一条对用户的药品质量投诉和药品不良反应应详细记录和调查处理。
Article 81: Any complaints on drug quality from the consumer and drug adverse reactions shall be recorded in detail and treated based on thorough investigation.
对河南省药品不良反应监测中心ADR 报告数据库中2006方法采用回顾性研究方法， 年～2010 年细辛脑注射液ADR/ADE 报告进行统计和分析。
Methods Relevant data was collected from database of Henan ADR Monitoring Center, statistical reviewed and analyzed, from 2006 to 2010.
方法采用回顾性研究方法，对2004 ~ 2005年河南省药品不良反应监测中心收集的中药注射剂不良反应病例报告进行统计和分析。
Method 3144 ADR reports collected by Henan Center for ADR Monitoring from 2004 to 2005 were analyzed using retrospective study method.
方法采用回顾性研究方法，对2004 ~ 2005年河南省药品不良反应监测中心收集的中药注射剂不良反应病例报告进行统计和分析。
Method 3144 ADR reports collected by Henan Center for ADR Monitoring from 2004 to 2005 were analyzed using retrospective study method.
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