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制定药品不良反应报告术语的使用要求。

Establishing requirements for the use of terms for reporting adverse drug reactions.

作者信息

Venulet J

机构信息

Council for International Organizations of Medical Sciences, Geneva, Switzerland.

出版信息

Int J Clin Pharmacol Res. 1992;12(2):61-4.

PMID:1428299
Abstract

The establishment of a project for the standardization of international reporting of adverse drug reactions (ADR), sponsored by the Council for International Organizations of Medical Sciences is described. The need to establish requirements for properly diagnosing a given suspected ADR and to describe it with the correct terms is demonstrated. However in view of the difficulties involved, it is suggested that the present deliberate approach needs to be reconsidered.

摘要

本文描述了由国际医学科学组织理事会发起的一个关于药品不良反应(ADR)国际报告标准化项目的设立情况。文中表明了确立正确诊断特定疑似药品不良反应并使用正确术语进行描述的要求的必要性。然而,鉴于其中涉及的困难,建议重新考虑当前这种审慎的方法。

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