结论：应加强ADR监测工作，降低漏报率，尤其应多途径收集过敏反应以外的药品不良反应，提高报表质量。
Conclusion: We should strengthen the monitoring of ADR, decrease the rate of misreporting, collect other ADR cases except allergic reaction in multiple tracks and enhance the report quality.
方法：对本院医务人员随机发放药品不良反应知识调查问卷273份，并将收集到的调查问卷进行整理与分析。
Methods: 273 knowledge questionnaires of adverse drug reactions were issued randomly to medical personnels in our hospital, and then were done classification and analysis.
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.
目的分析我院2005年收集的141份药品不良反应(adr)报告质量。
OBJECTIVE: To analyze the quality of 141 reports on adverse drug reaction in our hospital in 2005.
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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