第二条国家实行药品不良反应报告制度。
Article 2 the state implements the pharmaceutical side effect reporting system.
第七十一条国家实行药品不良反应报告制度。
Article 71 The State applies a system of report on adverse drug reaction.
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.
结论从填写完整性和报告时限性上都反映出药品不良反应报告质量有待提高。
Conclusion The quality of ADR reports should be improved in integrality and reporting time limit.
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.
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.
结论临床应重视药品不良反应报告和监测工作，以避免或减少药品不良反应发生。
Conclusion it should be paid more attention to the ADR report and monitoring in clinic in order to avoid or decrease the occurrence of ADR.
目的：通过分析我院近年来发生的中药药品不良反应报告（ADR）的特点指导临床用药安全。
Objective: To analyze the recent years of traditional Chinese medicine hospital adverse drug reactions (ADR) in clinical drug safety features.
参与企业质量体系建立、内部自检、外部质量审计、验证以及药品不良反应报告、产品召回等质量管理活动；
To participate in quality management activities such as establishment of the quality system, self-inspection, external quality audit, validation, adverse drug reaction reporting and product recalls;
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.
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.
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.
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.
目前药品不良反应报告存在着“药品不良反应报告少，新的和严重的药品不良反应报告少，药品生产企业药品不良反应报告少”的现状。
Now, "ADR are few reported, especially new and severe ADR reports are few, the ADR reported by drug production enterprises are also few".
方法回顾性分析本院药品不良反应(adr)监测中心提供的84例中药注射剂不良反应报告。
Methods a retrospective analysis was made on 84 reports of traditional Chinese medicine injection provided by adverse drug reaction (ADR) monitoring center in our hospital.
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：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.
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