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研究 FDA 批准药物标签中的药物基因组学信息,以促进精准医学的应用。

Study of pharmacogenomic information in FDA-approved drug labeling to facilitate application of precision medicine.

机构信息

National Center for Toxicological Research, US FDA, Jefferson, AR 72079, USA.

Department of Pharmacy and Therapeutics, University of Pittsburg, Pittsburgh, PA 15213, USA.

出版信息

Drug Discov Today. 2020 May;25(5):813-820. doi: 10.1016/j.drudis.2020.01.023. Epub 2020 Feb 4.

Abstract

Pharmacogenomics (PGx), studying the relationship between drug response and genetic makeup of an individual, is accelerating advances in precision medicine. The FDA includes PGx information in the labeling of approved drugs to better inform on their safety and effectiveness. We herein present a summary of PGx information found in 261 prescription drug labeling documents by querying the publicly available FDALabel database. A total of 362 drug-biomarker pairs (DBPs) were identified. We profiled DBPs using frequency of the biomarkers and their therapeutic classes. Four categories of applications (indication, safety, dosing and information) were discussed according to information in labeling. This analysis facilitates better understanding, utilization and translation of PGx information in drug labeling among researchers, healthcare professionals and the public.

摘要

药物基因组学(PGx)研究药物反应与个体遗传构成之间的关系,正在加速精准医学的发展。FDA 在已批准药物的标签中包含 PGx 信息,以更好地告知其安全性和有效性。我们通过查询公开的 FDALabel 数据库,从 261 份处方药标签文件中提取 PGx 信息,在此总结。共确定了 362 对药物-生物标志物(DBP)。我们根据生物标志物的频率及其治疗类别对 DBP 进行了分析。根据标签中的信息,讨论了四个应用类别(适应证、安全性、剂量和信息)。这种分析有助于研究人员、医疗保健专业人员和公众更好地理解、利用和转化药物标签中的 PGx 信息。

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