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评估临床试验中药物不良反应的记录方法。

Evaluation of methods for recording adverse drug reactions in clinical trials.

作者信息

Nilsson B S

机构信息

Astra Läkemedel AB, Södertälje, Sweden.

出版信息

Eur J Clin Microbiol Infect Dis. 1990 Jul;9(7):534-6. doi: 10.1007/BF01964298.

Abstract

Four methods used for obtaining information from patients on adverse drug reactions are reviewed on the basis of personal experience. In the development of new therapeutic drugs the method which records all events experienced by a patient during drug treatment is to be preferred as it increases the possibility of detecting unanticipated or previously unreported adverse reactions. Disadvantage of this method is that a high number of events not related to drug treatment may be recorded, causing problems in analysis of the data.

摘要

基于个人经验,对用于从患者处获取药物不良反应信息的四种方法进行了综述。在新治疗药物的研发过程中,记录患者在药物治疗期间经历的所有事件的方法更为可取,因为它增加了检测到意外或先前未报告的不良反应的可能性。这种方法的缺点是可能会记录大量与药物治疗无关的事件,从而在数据分析中产生问题。

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