期刊
CLINICAL PHARMACOLOGY & THERAPEUTICS
卷 95, 期 5, 页码 496-498出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/clpt.2014.17
关键词
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资金
- Clinical and Translational Science Award program, through the National Institutes of Health (NIH) National Center for Advancing Translational Sciences [UL1TR000427]
The US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) is a database for postmarketing drug safety monitoring and influences changes in FDA safety guidance documents such as drug labels. The number of cases in the FAERS has rapidly increased with the improvement of submission methods and data standards and thus has become an important resource for regulatory science. Although the FAERS has been predominantly used for safety signal detection, this study explored its utility for disease characteristics.
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