The Australian method of drug-event assessment. Special workshop--regulatory.

M L Mashford
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引用次数: 33

Abstract

In the Australian system, the major aim is to test individual reports for quality, judged entirely by the contents of the report. Prior knowledge of the adverse drug reaction profile of the drug is excluded. The items taken into account include timing (onset of the reaction), setting (nature of the disease, drugs, and diet), and laboratory information.

澳大利亚药物事件评价方法。特殊的研讨会——监管。
在澳大利亚的制度中,主要目的是测试个别报告的质量,完全由报告的内容来判断。不包括对药物不良反应的先验知识。考虑的项目包括时间(反应开始)、环境(疾病的性质、药物和饮食)和实验室信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Information Journal
Drug Information Journal 医学-卫生保健
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审稿时长
6-12 weeks
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