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Identifying Adverse Drug Events by Relational Learning

机译:通过关系学习识别不良药物事件

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摘要

The pharmaceutical industry, consumer protection groups, users of medications and government oversight agencies are all strongly interested in identifying adverse reactions to drugs. While a clinical trial of a drug may use only a thousand patients, once a drug is released on the market it may be taken by millions of patients. As a result, in many cases adverse drug events (ADEs) are observed in the broader population that were not identified during clinical trials. Therefore, there is a need for continued, post-marketing surveillance of drugs to identify previously-unanticipated ADEs. This paper casts this problem as a reverse machine learning task, related to relational subgroup discovery and provides an initial evaluation of this approach based on experiments with an actual EMR/EHR and known adverse drug events.
机译:制药行业,消费者保护组织,药物使用者和政府监督机构都对确定药物不良反应非常感兴趣。虽然一种药物的临床试验可能只使用一千名患者,但是一旦一种药物投放市场,它可能会被成千上万的患者服用。结果,在很多情况下,在更广泛的人群中观察到了药物不良事件(ADEs),而在临床试验中并未发现。因此,需要对药物进行持续的上市后监控,以识别先前未预料到的ADE。本文将这个问题归结为与相关亚组发现相关的逆向机器学习任务,并基于实际EMR / EHR和已知不良药物事件的实验,对该方法进行了初步评估。

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