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Automatically Recognizing Medication and Adverse Event Information From Food and Drug Administration’s Adverse Event Reporting System Narratives
BACKGROUND: The Food and Drug Administration’s (FDA) Adverse Event Reporting System (FAERS) is a repository of spontaneously-reported adverse drug events (ADEs) for FDA-approved prescription drugs. FAERS reports include both structured reports and unstructured narratives. The narratives often includ...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | JMIR Med Inform |
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| Κύριοι συγγραφείς: | , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Gunther Eysenbach
2014
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4288072/ https://ncbi.nlm.nih.gov/pubmed/25600332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2196/medinform.3022 |
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