WASHINGTON, D.C. (WPVI) -- A local congressman says the FDA grossly underestimated the harm caused by a contraceptive device. And he alleges the maker paid doctors kickbacks to recommend the device to ...
Even though it's no longer on the market, new data has emerged around potential side effects of the permanent birth control device Essure. The device, pulled from the US market two years ago amid ...
Since it was approved to go on the market in 2002, Essure, an implantable permanent contraceptive device, has been plagued by controversy. Thousands of women have filed grievances with the US Food and ...
Some 200 women in the UK who have reported being left in pain after having a – now discontinued – permanent contraceptive coil fitted (as opposed to the IUD and IUS, which can be removed at any time), ...
Thousands of women have complained to FDA about abdominal pain, headaches, and other complications after having the Essure coils implanted in their fallopian tubes. Qmed Staff U.S. FDA's Obstetrics ...
Federal health regulators plan to warn consumers more strongly about Essure, a contraceptive implant that has drawn thousands of complaints from women reporting chronic pain, bleeding and other health ...
RALEIGH (WTVD) -- Essure, a popular form of birth control, was marketed in 2002 as a permanent birth control without surgery. But, according to the Food and Drug Administration, more than 4,700 ...
At the request of the Food and Drug Administration, Leverkusen, Germany-based Bayer will now add a box warning and patient decision checklist to the label of its permanent birth control device Essure.
PHILADELPHIA (WPVI) -- The FDA slapped new restrictions on the sale of a controversial birth control device on Monday. The agency said some women aren't being properly informed of the risks of Essure ...
This article is brought to you by our exclusive subscriber partnership with our sister title USA Today, and has been written by our American colleagues. It does not necessarily reflect the view of The ...