| 提高药品不良反应报告表质量的若干问题探讨 |
| |
| 引用本文： | 郭辉,丁卫东,刘卫,王崎.提高药品不良反应报告表质量的若干问题探讨[J].中国药物警戒,2007,4(4):230-231. |
| |
| 作者姓名： | 郭辉 丁卫东 刘卫 王崎 |
| |
| 作者单位： | 徐州市药品不良反应监测中心,江苏,徐州,221005 |
| |
| 基金项目： | 徐州市卫生科技资助项目 |
| |
| 摘 要： | 通过分析2006年徐州市药品不良反应报告表存在的问题,提出在开展药品不良反应监测工作中应当采用报告表规范化、多专业合作、地区疑难报告表分析评估交流、上报人资格认定等多种方式以提高药品不良反应报告表的质量。
|
| 关 键 词： | 药品不良反应 报告表 质量 |
| 文章编号： | 1672-8629（2007）04-0230-02 |
| 修稿时间： | 2007-04-04 |
Several issues of improving the quality of statements of adverse drug reactions reports |
| |
| GUO Hui,DING Wei-Dong,LIU Wei,WANG Qi.Several issues of improving the quality of statements of adverse drug reactions reports[J].Chinese JOurnal of Pharmacovigilance,2007,4(4):230-231. |
| |
| Authors: | GUO Hui DING Wei-Dong LIU Wei WANG Qi |
| |
| Institution: | Center for ADR monitoring of Xuzhou Jiangsu (Xuzhou Jiangsu 221005, China |
| |
| Abstract: | This paper analyzes the existing problems for the quality of statements in adverse drug reac-tions reports of Xuzhou in 2006. The ADR monitoring should be more standardized,professional co-operation,regional exchanges in analysis and assessment for the difficult statements report and reported people were identified in the qualifications to improve the quality of ADR reports. |
| |
| Keywords: | Adverse drug reaction statements quality |
| 本文献已被 CNKI 维普 万方数据 等数据库收录！ |
