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Women Are Experiencing Essure Problems In Record Numbers

Women suffering from the side effects of the Essure birth control device have a Facebook Group to share their experience

Wednesday, November 15, 2017 - Facebook social media group Essure Problems has acted as an advocacy group for many women who have undergone Essure birth control implantation, and are suffering from the adverse side effects of the birth control device. Women in the group feel the efforts made by Bayer and the U.S. Food and Drug Administration to inform the public has been largely inadequate. Bayer AG is a German multinational, pharmaceutical conglomerate and the maker of the Essure medical device. Over 200 women have posted on Facebook Essure problems that they were not warned in advance by their doctors before having the Essure device implanted and thus were unable to make an informed decision.

As a result of the debilitating side effects of the Essure birth control device, the Facebook group's administrators report that approximately 9000 women have told the FDA that they have had to undergo hysterectomies in order to have the device that resembles a coiled, spring from a ball-point pen removed from their fallopian tubes. A hysterectomy is the same invasive surgical procedure that the device's implantation was intended to replace. Other adverse side effects that women are reporting include excessive menstrual bleeding, fatigue, allergies and autoimmune issues from the nickel/titanium plating of the device in patients with Nickel sensitivities. Many women report that they can not even get out of bed and certainly can not return to work. There have been incidences where the device has migrated to and perforated other organs within the body cavity causing serious infection and chronic, severe pain.

The number of women suffering from the debilitating side effects of Essure and being forced to undergo a hysterectomy is increasing each year at an alarming rate. A hysterectomy is the surgical removal of the uterus, cervix, ovaries, fallopian tubes and other tissue. From an initial count of around 90 reported incidences in 2009, the number of adverse event reports, i.e., emergency hysterectomies reported to the FDA has increased to over 3000 in 2016. In the first quarter of 2017, the database received over 2000 new reports. These figures do not reflect the over 300 fetal deaths that are now being attributed to the device's malfunction.

Bayer has voluntarily stopped selling the device in all countries with the exception of the lucrative US market. Many women feel that Bayer and the FDA have downplayed the seriousness of the product's side effects and thousands of women have chosen to sue Bayer. The group is demanding that the FDA remove the product from the US market until studies of the product's safety have concluded. Bayer concedes that they have spent approximately one half a billion dollars on settling lawsuits and legal expenses related to Essure lawsuits.

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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.