药品不良反应监测具有计算机化的倾向。
The surveillance of drug adverse reaction is going to be computerized.
目的推动药品不良反应监测工作的深入开展。
Objective to promote the ADR monitoring in-depth development.
目的：探讨如何优化“全国药品不良反应监测网络”的软件功能。
OBJECTIVE:To discuss the method to optimize the function of current "Nationwide Adverse Drug Reaction Monitoring Network".
结论应重视药品不良反应监测，合理用药，预防过敏性休克发生。
Conclusion We should be emphasize ADR monitoring, rational use of drug and prevention of AIAS.
方法针对基层药品不良反应监测工作现状，剖析存在的问题及原因。
Methods Through discussion on situation of grass-roots ADR monitoring, we analyzed the existing problems and reasons.
结果全国基层药品不良反应监测机构建设尚不完善，诸多问题亟需解决。
Results it needs urgent solutions that national primary ADR Monitoring system is imperfect and impact sustainable development.
药品不良反应报告质量的评价与控制是药品不良反应监测工作的基本要求。
The evaluation and control for adverse drug reaction (ADR) reports quality are basic requirements for ADR monitoring.
结果与结论提出进一步推动药品不良反应监测工作深入开展的建议和对策。
Results and Conclusions Many countermeasures to further promote the ADR monitoring in-depth development are proposed.
目的了解抗肿瘤药物引起的不良反应，为深入开展药品不良反应监测工作提供依据。
Objective To investigate the adverse drug reaction (ADR) induced by antineoplastics, and provide bases for deep ADR monitoring.
结论不良反应定量信号检测系统的建立可以极大地提高药品不良反应监测工作的效率。
Conclusions Establishment of quantitative signal detection system can greatly enhance the efficiency of ADR monitoring.
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.
药品安全性问题是全球共同关注的焦点，药品不良反应监测是发现上市药品安全隐患的重要手段。
Drug safety problem is a global focus. ADR monitoring is an important method on finding drug safety problems.
方法：回顾我国药品不良反应监测专业机构的建立，阐述其工作职责及内容，评述已开展的工作。
METHODS:To review the establishment of specialized agency for monitoring ARDs in China; to describe its working duty and content; to comment the work which has been carried out.
结论：在门诊输液室建立医、护、药合作的药品不良反应监测体系，为门诊输液安全提供了有利条件。
Conclusion: Establishing the drug adverse reaction monitor system in the outpatient transfusion room can improve transfusion safety.
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.
目的分析本院药品不良反应报告情况，为临床合理用药提供参考，推进我院药品不良反应监测报告工作的开展。
Aim to supply optimal reference for the rational clinical use of drugs and promote the monitoring of adverse drug reactions in Huainan First Municipal Peoples Hospital.
本文强调了建立药品不良反应监测的重要性，论述了我国开展药品不良反应监测的现状，提出了今后的工作要点。
This paper stresses the importance of establishing an monitoring system for adverse reactions of drugs, and describes the present status in China. The main points in future work are put forward.
方法：对上海市药品不良反应监测中心药品不良反应数据库内413例静脉滴注用中药注射液不良反应报告进行汇总分析。
Methods; An analysis was conducted on 413 reports of adverse drug reactions resulted from Chinese Traditional medicine Injection in venoclysis.
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.
方法：查阅国内、外文献以及我国和世界卫生组织药品不良反应监测中心数据库，分析《ADR信息通报》发布的阿昔洛韦安全性监测情况及不合理用药现状。
METHODS: Through the research of domestic and overseas literatures, WHO and national ADR database to analyse the causes of the bulletin of acyclovir and current situation of unreasonable drug use.
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.
现在，几乎有100个国家已经建立起国家体系，将药品不良反应向由世卫组织合作中心(乌普萨拉监测中心)管理的数据库做出报告。
Nearly 100 countries now have national systems in place to report ADRs to the database managed by the WHO Collaborating Centre, the Uppsala Monitoring Centre.
目的利用计算机、网络技术开展药品不良反应(adr)监测。
Objective to use computer and network technologies for Adverse Drug Reaction (ADR) monitoring.
目的：加强药品不良反应(adr)监测，促进合理用药。
Objective: Strengthening of adverse drug reactions (ADR) monitoring and promoting rational drug use.
方法设计药品不良反应临床简报系统软件，利用简报系统监测药品不良反应具有方便快捷、效率高等优点。
Methods Design adverse drug reaction clinical briefing system software, use the advance of the briefing system in monitoring the adverse drug reactions with fast and convenient and high efficiency.
结论监测药品不良反应，预防药品不良反应的发生，是促进合理用药及保障用药安全的有效手段。
Conclusion Monitoring ADR is the effective method to prevent the occurrence of ADR, promote reasonable drug application and ensure the safety of drug use.
目的探讨医疗机构开展药品不良反应(adr)监测工作的模式。
Objective to discuss on the monitoring mode of adverse drug reactions (ADR) that can be used by the medical organization.
因此，开展药品不良反应报告和监测管理工作已成为关系民生的重要方面，是深化医药卫生体制改革的必然要求。
Therefore, the adverse drug reaction monitoring report and management has become an important aspect of the relationship between people is deepening the reform of medical care system requirement.
因此，开展药品不良反应报告和监测管理工作已成为关系民生的重要方面，是深化医药卫生体制改革的必然要求。
Therefore, the adverse drug reaction monitoring report and management has become an important aspect of the relationship between people is deepening the reform of medical care system requirement.
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