Spontaneous Reporting on Adverse Events by Consumers in the United States: An Analysis of the Food and Drug Administration Adverse Event Reporting System Database

BACKGROUND: Voluntary reports on adverse events (AEs) submitted by consumers have been facilitated through the MedWatch program in the United States (US), but few studies have described the characteristics of voluntary reports. OBJECTIVE: The aim of this study was to reveal the characteristics of cu...

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Detalles Bibliográficos
Autores principales: Toki, Tadashi, Ono, Shunsuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984610/
https://www.ncbi.nlm.nih.gov/pubmed/29725886
http://dx.doi.org/10.1007/s40801-018-0134-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984610/
https://www.ncbi.nlm.nih.gov/pubmed/29725886
http://dx.doi.org/10.1007/s40801-018-0134-0

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