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Development of an automated assessment tool for MedWatch reports in the FDA adverse event reporting system
Objective: As the US Food and Drug Administration (FDA) receives over a million adverse event reports associated with medication use every year, a system is needed to aid FDA safety evaluators in identifying reports most likely to demonstrate causal relationships to the suspect medications. We combi...
Enregistré dans:
| Publié dans: | J Am Med Inform Assoc |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Oxford University Press
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7651970/ https://ncbi.nlm.nih.gov/pubmed/28371826 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jamia/ocx022 |
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