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Participatory surveillance of diabetes device safety: a social media-based complement to traditional FDA reporting

BACKGROUND AND OBJECTIVE: Malfunctions or poor usability of devices measuring glucose or delivering insulin are reportable to the FDA. Manufacturers submit 99.9% of these reports. We test online social networks as a complementary source to traditional FDA reporting of device-related adverse events....

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Main Authors: Mandl, Kenneth D, McNabb, Marion, Marks, Norman, Weitzman, Elissa R, Kelemen, Skyler, Eggleston, Emma M, Quinn, Maryanne
Formato: Artigo
Idioma:Inglês
Publicado: BMJ Publishing Group 2014
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4078274/
https://ncbi.nlm.nih.gov/pubmed/24355131
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/amiajnl-2013-002127
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