药物不良反应的标准化评估:法国采用的方法。特殊的研讨会——临床。

B Begaud
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引用次数: 22

摘要

自1977年以来,法国用于评估药物不良反应(adr)的方法基于三个阶段的过程:评估三个时间标准(挑战、挑战和再挑战);评估临床和生物学结果;并结合时间和症状评估,获得3度的整体评分(1:怀疑,2:可能,3:可能)。文献数据(以前报告的或未报告的ADR)是完全分开评估的;因此,该方法对检测新的adr具有良好的灵敏度。
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Standardized assessment of adverse drug reactions: the method used in France. Special workshop--clinical.

The method used in France since 1977 for assessing adverse drug reaction (ADRs) is based on a three-stage process: assessment of three chronological criteria (challenge, dechallenge, and rechallenge); assessment of clinical and biological findings; and a combination of chronological and symptomatological assessments to obtain a 3-degree global score (1: doubtful, 2: possible, 3: probable). Bibliographical data (previously reported or unreported ADR) are assessed quite separately; thus, the method has a good sensitivity for detecting new ADRs.

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来源期刊
Drug Information Journal
Drug Information Journal 医学-卫生保健
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