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Miscategorization of Deaths in the US Food and Drug Administration Adverse Events Database

This database study assesses the misclassification of death reports for 2 medical devices within the US Food and Drug Administration’s Manufacturer and User Facility Device Experience database.

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Detalles Bibliográficos
Publicado en:JAMA Intern Med
Autores principales: Meier, Lily, Wang, Elizabeth Y., Tomes, Madris, Redberg, Rita F.
Formato: Artigo
Lenguaje:Inglês
Publicado: American Medical Association 2019
Materias:
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6784806/
https://ncbi.nlm.nih.gov/pubmed/31589249
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamainternmed.2019.4030
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