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A Florida woman has filed a product liability lawsuit against Teva Pharmaceuticals, alleging that she suffered sever complications from a Paragard intrauterine device (IUD), after the birth control migrated out of her uterus and embedded into her colon.
Yolanda Hudson filed a ParaGard IUD lawsuit in Florida state court on March 4, according to a recent report by Law360.com.
The complaint alleges that Hudson had the ParaGard copper IUD inserted in March 2008. Although the birth control device is designed to remain in place for up to 10 years, Hudson began experiencing severe complications a year later and it was discovered that the IUD had perforated her uterine wall and migrated outside the uterus, ultimately embedding in the colon. As a result, Hudson required surgery to have part of her colon removed.
According to allegations raised in the lawsuit, Teva Pharmaceuticals failed to adequately warn women and their doctors about the risks associated with the Paragard copper IUD, which is promoted as a safe and effective form of long-acting birth control. In addition to problems with migration, Hudson indicates that side effects of the ParaGard IUD could include intrauterine pregnancy, ectopic pregnancy, pelvic infection, expulsion, Wilson Disease, vaginal bleeding, septic abortion, and other complications.
The lawsuit charges Teva with failure to warn, negligence, breach of warranty, misrepresentation, and designing a defective product. The lawsuit seeks $15 million in damages for pain and suffering, disability, physical impairment, disfigurement, mental anguish, inconvenience, loss of capacity for enjoyment of life and also seeks punitive damages against the company for at least three times the compensatory damages.
Mounting Lawsuits Over IUD Birth Control
ParaGard is a copper IUD, where a T-shaped plastic frame is wrapped with copper wire coils, which is designed to produce an inflammatory reaction in the uterus that is toxic to sperm. The device is designed to remain in place for up to 10 years after insertion.
Hudson’s complaint comes amid a mounting number of similar lawsuits that have been filed over another type of IUD birth control, which is sold by Bayer under the brand name Mirena.
The Mirena IUD does not feature copper, but rather is designed to release a type of progestin after the T-shaped plastic device is inserted into the uterus.
According to similar allegations raised in dozens of Mirena IUD lawsuits filed by women throughout the United States, Bayer failed to adequately warn about the risk of migration and perforation, which has often been seen long after the device is inserted. The complaints argue that if women had been provided more detailed and accurate warnings about the risks, many severe complications from Mirena IUD could have been avoided.