85% of Bayer Essure Adverse Event Reports Submitted Last Year Linked to Device Removal: FDA
Abdominal pain and bleeding were the two most frequently reported Essure adverse events, according to the FDA.
Abdominal pain and bleeding were the two most frequently reported Essure adverse events, according to the FDA.
The analysis comes from postmarketing surveillance data on Essure recipients, which was required by the FDA after Bayer pulled the birth control implant from the market in 2018.