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Safety reporting of Essure medical device: a qualitative and quantitative assessment on the FDA manufacturer and user facility device experience database in 2018

BACKGROUND: There have been numerous cases of adverse events since the introduction of Essure medical devices for sterilization in 2002. This study analyzed the safety event reports of the Essure reported in the Manufacturer and User Facility Device Experience (MAUDE). METHODS: A retrospective analy...

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Detalles Bibliográficos
Autores principales:	Zou, Chenyu, Davis, Brandy, Wigle, Patricia R., Hincapie, Ana L., Guo, Jeff Jianfei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Reproductive Health
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374426/ https://www.ncbi.nlm.nih.gov/pubmed/37519343 http://dx.doi.org/10.3389/frph.2023.1172927

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