the reporting odds ratio and its advantages over proportional reporting ratio
Summary
Introduction
在臨床試驗中要計算AR與RR是很簡單的,可是以臨床試驗來評估罕見不良事件發生的風險,卻難以達到我們預期的成果。因此,由製藥廠還有主管機關所提供的一般族群資料,特別是自願的不良事件報告(spontaneous reports of adverse events),就變成用藥安全監控一個很重要的資料來源。而 A problem with the PRRAnalogy with the PMRThe MOR and the RORDiscussionReferencesReviewThe Words
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Paper information
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page revision: 11, last edited: 24 Oct 2010 00:39