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Bayer Stands Behind Essure

In spite of public outcry that has seen Essure sales plummet, Bayer continues to sell the product to unsuspecting women as if nothing is wrong

Thursday, August 2, 2018 - Essure permanent birth control sales are reported to have fallen around 90% over the course of the last year. The decline has prompted Bayer, maker of Essure to voluntarily remove the product from the market effective at the end of 2018. Bayer blames adverse publicity for the drop in Essure sales and refuses to admit blame for Essure's side effects. Bayer's Essure website continues to promote the fact that Essure is implanted through the vagina without the need for invasive surgery and is done in the comfort and convenience of the doctor's office.

Essure is sold for its convenience and is effective in 99.8 percent of patients. Bayer gives the reason for taking Essure off of the market as being that Essure is no longer a viable business model. Bayer continues to believe that the device is safe in spite of the fact that tens of thousands of women have documented the device's life-threatening adverse side effects. Essure.com reassures potential patients by saying "As a minimally invasive procedure, Essure placement requires no cutting, leaves no visible scars, and can be performed in your doctor's office."

Essure is a spring-like device resembling the spring in a retractable ballpoint pen. Two Essure devices are implanted through the vagina, one into each of the Fallopian tubes. Essure is designed with fibers to create inflammation and use the body's natural response to create scar tissue to block fertilization. It takes three months for Essure to become effective.

In 2018, The US Food and Drug Administration (FDA) demanded that Essure doctors and patients fill out a detailed questionnaire to make sure that prospective Essure patients were aware of the health consequences of the device before having it implanted. It was assumed that the questionnaire would provide women with pertinent, accurate information about Essure's side effects to help them to make a more informed decision as to which birth control method to choose. Surveys, however, of women that have recently received Essure indicate that doctors have ignored the FDA's questionnaire and continue to recommend Essure. Women questioned are surprised when told that thousands of women that chose Essure have experienced heavy periods, bleeding between periods, missed periods, migraine headaches, and weight gain, and allergic reactions and auto-immune problems as a result of Essure, and have sought to have Essure removed. Very few doctors are trained and capable of removing Essure should the need arise. Essure removal can require a patient to travel thousands of miles at their own expense to see a qualified Essure removal surgeon. Essure removal is expensive and is not usually covered by health insurance.

Essure's removal from the market leaves a woman with fewer options for permanent birth control such as hysterectomy and tubal ligation. Both procedures require admission to a hospital, surgery, and general anesthesia. Ironically, Essure removal surgery can require a hysterectomy or tubal ligation, the same radical surgical procedures that the Essure patient originally sought to avoid, and leave a woman permanently sterile. This is why lawyers handling Essure permanent birth control cases continue to fight for the safety of the patients.

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Onder Law is a St. Louis personal injury law firm handling serious injury and death claims across the country. Its mission is the pursuit of justice, no matter how complex the case or strenuous the effort. The Onder Law Firm has represented clients throughout the United States in pharmaceutical and medical device litigation such as Pradaxa, Lexapro and Yasmin/Yaz, where the firm's attorneys held significant leadership roles in the litigation, as well as Actos, DePuy, Risperdal and others, and other law firms throughout the nation often seek its experience and expertise on complex litigation.