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The FDA May Have Underestimated Essure-related Fetal Death Numbers

An FDA whistleblower has uncovered more deaths caused by Essure using advanced data search measures

Wednesday, November 22, 2017 - The Essure medical device has been sold by Bayer in the US since 2002 as a minimally invasive procedure, requiring no cutting to insert, leaving no visible scars, and performed in the comfort of the doctor’s office. In other words, a convenient, safer method of effective birth control. The device has been known to cause fetal death in a small number of patients however that number may have been vastly underestimated.

The FDA reports that to date, eleven deaths including 5 fetal deaths have occurred in women who became pregnant after having doctors implant the Essure birth control device in them. According to Reuters, however, the U.S. Food and Drug Administration may have "greatly underestimated" this number. Upon investigation into the FDA's adverse events database, independent private analyst Madris Tomes found that over 300 fetal deaths might be linked to using Essure. The reason for the differences between the FDA's number of 5 fetal deaths and Tomes' estimate of over 300 is that Tomes uses a more specific content search and does not simply search the database headers. Tomes is a bit of a whistleblower as she once worked as an FDA analysts and left in order to start a firm that more closely and accurate analyses public government data. The FDA's adverse drug event database is one such source of data. The number of fetal deaths found by Tomes, in conjunction with the 30,000 plus member Facebook group entitled "Essure Problems", has drawn the attention of US government officials. U.S. Representative Mike Fitzpatrick has written to the FDA requesting that the agency address the "immense discrepancies" as he put it in the Essure fetal death numbers.

In addition to the fetal death numbers, the FDA has been inundated with thousands of complaints from women who use Essure. The complaints are numbered and varied and include suffering from headaches, body aches, nausea, abnormal bleeding, chronic fatigue, allergies and autoimmune issues. Women have reportedly lost their jobs from being unable to return to work and many have not even been unable to get out of bed for months after having the device implanted. The device which has been marketed by Bayer as "reversible birth control" is virtual unremovable as most are encased by so much scar tissue that removing it would entail a full and radical hysterectomy, the exact surgery that implanting the Essure device was designed to avoid.

Recently Bayer has issued a warning to health officials that the product has been reported to cause serious, life-threatening adverse side effects in women using the birth control device. Some patients implanted with the Essure System for Permanent Birth Control have experienced and/or reported adverse events, including "perforation of the uterus and/or fallopian tubes, identification of inserts in the abdominal or pelvic cavity, persistent pain, and suspected allergic or hypersensitivity reactions. If the device needs to be removed to address such an adverse event, a surgical procedure will be required." This warning validates the concerns of the thousands of women who are filing Essure complications lawsuits, suing Bayer for their negligence in failing to warn them of the many health complications of using Essure.

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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.