40,000 Women Have Suffered From Essure, Only About 1,000 Lawsuits Filed. What’s Wrong?
Since the Essure contraceptive device first received FDA approval in 2002, the federal regulatory agency has received 10,000 complaints about the device. Over the same period, the manufacturer, Bayer, has gotten an additional 30,000 reports of adverse events related to Essure. These events include cramping, dizziness, nausea and vomiting, perforation of the organs, fluid build-up in the blood (hypervolemia), osteoporosis and chronic pain that lasts a lifetime. In many cases, the device cannot be retrieved, so a complete hysterectomy must be performed. These symptoms have affected 1 in every five women who have had the device implanted – yet...
Read More