Increasing Patient Engagement in Pharmacovigilance Through Online Community Outreach and Mobile Reporting Applications: An Analysis of Adverse Event Reporting for the Essure Device in the US

BACKGROUND: Preparing and submitting a voluntary adverse event (AE) report to the US Food and Drug Administration (FDA) for a medical device typically takes 40 min. User-friendly Web and mobile reporting apps may increase efficiency. Further, coupled with strategies for direct patient involvement, p...

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Detalles Bibliográficos
Autores principales: Bahk, Chi Y., Goshgarian, Melanie, Donahue, Krystal, Freifeld, Clark C., Menone, Christopher M., Pierce, Carrie E., Rodriguez, Harold, Brownstein, John S., Furberg, Robert, Dasgupta, Nabarun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4656696/
https://www.ncbi.nlm.nih.gov/pubmed/26635479
http://dx.doi.org/10.1007/s40290-015-0106-6

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