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新疆7所医院药品不良反应监测报告工作督查分析

耿东升 王晓娟 赵文燕

中国药业2017,Vol.26Issue(19):78-81,4.
中国药业2017,Vol.26Issue(19):78-81,4.DOI:10.3969/j.issn.1006-4931.2017.19.023

新疆7所医院药品不良反应监测报告工作督查分析

Supervision and Analysis of Reports and Monitoring of Adverse Drug Reaction in Seven Hospitals in Xinjiang

耿东升 1王晓娟 1赵文燕1

作者信息

  • 1. 中国人民解放军新疆军区药品仪器检验所,新疆乌鲁木齐 830063
  • 折叠

摘要

Abstract

Objective To supervise the development of the reports and monitoring of adverse drug reaction ( ADR ) in hospitals. Methods The specially formulated checklist was adopted as the supporter, by the way of consulting of work institution and records, on-site ac-cessing to the table of adverse drug reaction/event, asking and answering questions, publicizing teaching and the mentoring, reviewing comments, the jobs of the reports and monitoring of ADR were inspected and supervised in seven hospitals in Xinjiang. Results The report rate of ADR in hospital was commonly lower. The management system and records of ADR reports and monitoring were imperfec-tion. The doctor′s initiative to report ADR has not yet been stimulated. Chinese patent drugs and injections of antibiotics were still main drugs that induced to ADR. Conclusion The function of regulatory oversight of the drug administration department should be strength-ened and brought into play so that the reports and monitoring of ADR in hospitals are paid attention to and implemented.

关键词

监督/检查/药品不良反应/药品不良反应报告/药品不良反应监测/医院

Key words

supervision/inspection/adverse drug reaction/report of adverse drug reaction/monitoring of adverse drug reaction/hospital

分类

医药卫生

引用本文复制引用

耿东升,王晓娟,赵文燕..新疆7所医院药品不良反应监测报告工作督查分析[J].中国药业,2017,26(19):78-81,4.

中国药业

OACSTPCD

1006-4931

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