| 如何完善我国药品不良反应监测体系 |
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| 引用本文： | 郭莹,王胜兴.如何完善我国药品不良反应监测体系[J].中国药物警戒,2010,7(2):95-97. |
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| 作者姓名： | 郭莹 王胜兴 |
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| 作者单位： | 沈阳药科大学工商管理学院,辽宁,沈阳,110016 |
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| 摘 要： | 目的探讨如何使我国药品不良反应监测体系更加完善。方法主要采用文献查阅法和借鉴国外的成功经验。结果与结论通过完善相关法律法规、药品不良反应报告制度、药品不良反应监测体系、中药不良反应监测制度等多个环节的措施来完善我国药品不良反应监测规制。
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| 关 键 词： | 药品不良反应 监测 法律法规 |
Perfection of Adverse Drug Reaction Monitoring System in China |
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| GUO Ying,WANG Sheng-xing.Perfection of Adverse Drug Reaction Monitoring System in China[J].Chinese JOurnal of Pharmacovigilance,2010,7(2):95-97. |
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| Authors: | GUO Ying WANG Sheng-xing |
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| Institution: | (College of Business Administration, Shenyang Pharmaceutical University, Liaoning Shenyang 110016, China) |
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| Abstract: | Objective It discusses mainly how to perfect our ADR monitor system. Methods It applies mainly the literature method and uses the foreign successful experience. ResuJts and Conclusion By perfecting the relative law and regulation, ADR report system, ADR monitor system, the ADR of tradional Chinese medicine monitoring system, all of these methods will help to perfect our ADR monitor system. |
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| Keywords: | adverse drug reaction（ADR） monitor law and regulation |
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