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Bayer Cancels Future Sales of Essure Birth Control

What to Know

  • Bayer will halt sales of Essure, a controversial birth control device that consists of metal coils inserted into the fallopian tubes

  • A vocal group of Essure patients has long claimed the contraceptive can cause allergic reactions, chronic pain and fatigue

  • In 2013, the I-Team was first to report on questions about patient Kim Hudaks medical records in the clinical trials

After years of outcry from patients who say theyve suffered excruciating side-effects, Bayer has opted to halt sales of Essure, a controversial birth control device that consists of metal coils inserted into the fallopian tubes.

The pharmaceutical giant says its decision to cancel the product at the end of 2018 has nothing to with safety concerns.

In a statement to the I-Team, Courtney Mallon, a Bayer spokesperson, said the company is discontinuing Essure because U.S. sales are in decline.

“We feel it is very important to emphasize that this is not a recall situation,” Mallon wrote. “This is purely a business decision.

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Though Bayer continues to stand behind the safety of Essure, a vocal group of Essure patients has long claimed the contraceptive can cause allergic reactions, chronic pain and fatigue. Some patients have even reported the metal coils migrating and puncturing internal organs.

“Their sales were down,” said Angie Firmalino, the founder of a Facebook group that catalogued thousands of Essure complaints. “I think thats a credit to our group raising awareness about this device. They keep saying that were spreading misinformation but were spreading the truth.”

Dolly Pena, an Essure patient currently looking for a doctor who can safely remove the coils, cheered Bayers decision to cancel the product.

“We want this to be out of the market so no other women will be harmed,” Pena said.

“This is a huge battle that weve won,” said Kim Hudak, an Essure patient who participated in the clinical trials that resulted in the products FDA approval.

In 2013, the I-Team was first to report on questions about Hudaks medical records in the clinical trials. Though she reported experiencing severe pelvic pain in seven of eight years after being implanted with Essure, researchers administering the study repeatedly marked Hudaks comfort wearing the device as “excellent.”

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“It is disheartening because I know what I went through during the clinical trials and the problems that I was experiencing that never made it into the permanent records. They knew there was a problem. They discarded it,” Hudak said.

Bayer says the FDA examined the clinical trial documentation and found no evidence researchers purposefully modified patient responses to reflect more positive results.

Scott Gottlieb, the FDA Commissioner, released a public statement affirming federal regulators still consider Essure to be a safe form of contraceptive, but he also said the FDA wants Bayer to complete government-ordered research to investigate painful side-effects being reported by patients.

“The decision today to halt Essure sales also follows a series of earlier actions that the FDA took to address the reports of serious adverse events associated with its use,” Gottlieb said. “We expect Bayer to meet its postmarket obligations concerning this device.”

Aside from regulatory scrutiny, Bayer is still facing several lawsuits from patients who want the right to sue the pharma firm over issues related to Essure. The company said canceling the product had nothing to do with those lawsuits.

“I think Bayer pulling this from the market is probably going to be favorable to us in the eyes of the courts,” Firmalino said.

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NBC

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