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| 药品不良反应信息监管的思考 | |
| 引用本文： | 易孟,田侃. 药品不良反应信息监管的思考[J]. 中国药事, 2010, 24(9): 837-839,880 |
| 作者姓名： | 易孟 田侃 |
| 作者单位： | 南京中医药大学经贸管理学院,南京,210046 |
| 摘 要： | 目的完善药品不良反应信息监管制度。方法以药品不良反应案例为切入点,分析药品不良反应信息监管中存在的问题并提出建议。结果与结论完善多级药品不良反应监测体系、完善两级信息发布制度、完善突发药品不良事件的监管机制,为政府监管和公众安全用药提供有效的信息。 |
| 关 键 词： | 药品不良反应 信息 监管 |
Thinking about the Information Monitoring System of ADR |
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| Yi Meng,Tian Kan. Thinking about the Information Monitoring System of ADR[J]. Chinese Pharmaceutical Affairs, 2010, 24(9): 837-839,880 | |
| Authors: | Yi Meng Tian Kan |
| Affiliation: | Yi Meng and Tian Kan (The Economic and Trade Management College,Nanjing University of TCM,Nanjing 210046) |
| Abstract: | Objective Improve the information monitoring system of ADR. Methods Based on the cases of ADR,analyze the problems of ADR information supervision and make recommendations. Results and Conclusion Perfect the multi-level monitoring system for ADR,the two-stage information release system and the regulatory mechanism of unexpected adverse drug events.Provide effective information for government regulation and public safety for the drug. |
| Keywords: | ADR information supervision |
| 本文献已被 CNKI 维普 万方数据 等数据库收录！ | |