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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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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2014
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| Matèries: | |
| Accés en línia: | 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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