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Standardizing adverse drug event reporting data
BACKGROUND: The Adverse Event Reporting System (AERS) is an FDA database providing rich information on voluntary reports of adverse drug events (ADEs). Normalizing data in the AERS would improve the mining capacity of the AERS for drug safety signal detection and promote semantic interoperability be...
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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4142531/ https://ncbi.nlm.nih.gov/pubmed/25157320 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2041-1480-5-36 |
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