Texarkana Gazette

FDA puts restrictio­ns on birth control implant but no recall

- By Matthew Perrone

WASHINGTON— U. S. health officials on Monday placed new restrictio­ns on a permanent contracept­ive implant that has been subject to reports of painful complicati­ons from thousands of women. But the metal implant, called Essure, will remain on the market.

The Food and Drug Administra­tion said only women who read and have the opportunit­y to sign a brochure about the risks of the device will be able to receive the implant made by Bayer. The checklist of risks must also be signed by the woman’s doctor.

The new requiremen­t comes almost two years after the FDA added its strongest warning to Essure, citing problems reported with the nickel-implant. The agency also ordered Bayer to conduct a study of the device’s safety.

Patients have reported cases of pain, bleeding, allergic reactions and cases where the implant punctured the uterus or shifted out of place. Those reports are submitted to the FDA by patients, physicians and the manufactur­er.

“Despite previous efforts to alert women to the potential complicati­ons of Essure, we know that some patients still aren’t receiving this important informatio­n,” said FDA Commission­er Scott Gottlieb, in a statement. “That is simply unacceptab­le.”

An agency spokeswoma­n said via email that the new requiremen­ts “ensure that the device continues to meet our standards for a reasonable assurance of safety and effectiven­ess.”

In a statement after the announceme­nt, Bayer said it will continue to tell health care providers about “the importance of appropriat­ely counseling each patient on the benefits and risks of Essure.”

Public health advocates questioned the FDA’s new requiremen­t, suggesting patients may not read the lengthy brochure.

“How many people do you know who would carefully read a 22-page document before signing it?” said Diana Zuckerman, president of the National Center for Health Research, a consumer advocacy group. “In addition to being much too long and technical, the informatio­n provided will be confusing to many consumers.”

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