药物的不良反应报告也表明有问题存在。
Reports of adverse drug reactions may also indicate that all is not well.
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.
方法对104例阿奇霉素不良反应报告进行分析。
Methods an analysis was conducted on 104 reports of adverse drug reactions related with Azithromycin.
这些规定旨在确保质量控制、建立不良反应报告机制和规范成分标签。
The regulations aim to ensure quality control, reporting of adverse effects and proper labelling of contents.
方法：通过97例临床不良反应报告表进行回顾性分析。
METHODS: Retrospective analysis were carried out by the reports of clinical ADR in 97 cases.
方法：对收集的74例不良反应报告进行统计分析及评价。
Methods: The reports on 74 case of ADR collected by ADR monitoring group of our hospital were counted, classified and analyzed.
随着临床的广泛使用，消渴丸引起的不良反应报告也日渐增多。
With being widely used in clinic, more and more ADR cases of Xiaoke Wan have been reported.
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.
方法对2008年度收集到的136例抗感染药致不良反应报告进行回顾性分析。
Methods the year 2008 in our hospital collected 136 cases of adverse reactions to the report of anti-infective agents were retrospectively analyzed.
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.
过去二十年，FDA接到了141个牙科使用汞合金后的不良反应报告，但没有导致死亡病例。
Over the past 20 years, according to Runner, the FDA has received 141 adverse event reports regarding dental amalgams, with none resulting in death.
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.
至今为止FDA还没收到接受所述组织治疗的患者不良反应报告（例如，传染病传播到接受者）。
To date, FDA has not received reports of adverse reactions (e. g. , transmission of communicable disease to recipients) in any patients who may have received the tissues in question.
方法对我院2005年2月至2007年9月收集的95例抗肿瘤药物的不良反应报告进行回顾性分析。
Methods 95 ADR reports collected between February 2005 and September 2007 in our hospital have been analyzed retrospectively.
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.
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.
方法采用回顾性调查方法，对我院2004年填报的113例加替沙星注射液致不良反应报告进行统计、分析。
METHODS: a retrospective investigation was carried out to analyze statistically 113 reported cases of ADRS of Gatifloxacin injection in Our hospital in 2004.
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.
方法：采用回顾性调查方法，对我院2004年填报的127例左氧氟沙星注射液致不良反应报告进行统计、分析。
METHODS:A retrospective investigation was carried out to analyze statistically 127 reported cases of ADRs of levofloxacin in our hospital in 2004.
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.
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".
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".
应用推荐