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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Publicat a:Pharmaceut Med
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Springer International Publishing 2015
Matèries:
Original Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4656696/
https://ncbi.nlm.nih.gov/pubmed/26635479
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40290-015-0106-6
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