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FDA Whistleblower Madris Tomes Was One of the First to Suspect Essure Problems

One of the most important persons involved in exposing the dangers that the Essure birth control device poses is former FDA analyst Madris Tomes

Friday, November 9, 2018 - Ms. Tomes left the FDA and started her own computer company after she recognized that there were problems inherent in the way the FDA collected and analyzed its adverse events database. Ms. Madris left the FDA when she suspected that the FDA knew that the Essure birth control device was making women deathly ill and looked the other way. Madris also discovered that Essure was responsible for several hundred fetal deaths, not the 5 or so the FDA and Bayer took responsibility for.

Essure is designed to elicit an inflammatory response from the tissues of the Fallopian tubes when inserted into the vagina and maneuvered into place. Essure consists of two nickel-titanium, stainless steel coils wrapped with polyethylene terephthalate fibers. Scar tissue is then formed around the Essure device over an initial three month period, blocking contraception. This is where a woman's problems begin. Some women have metal hypersensitivity causing severe allergic reactions such as "debilitating pelvic pain, joint pain, fibromyalgia, chronic degenerative diseases, migraines, chronic fatigue syndrome, autoimmune disorders, menstrual abnormalities, numbness in the extremities, severe allergic reactions, dizziness, rashes, unexplained fevers, multiple UTI's and so much more," according to www.Essureproblems.com. When infections occur at the Essure site, the device is attacked by the body's natural immune system. As a result of metal hypersensitivity infections, Essure can break apart or break free from the Fallopian tubes and migrate and penetrate the uterus. Uterine contractions to expel the foreign device only sinks Essure's sharp metal edges deeper and deeper into the uterine tissue until the pain becomes so excruciating that an emergency hysterectomy is the only course of action. But let us not forget Bayer's reassurances that Essure can be inserted in the comfort and convenience of your doctor's office. In addition, a sometimes overlooked consequence of Essure migration out of the Fallopian tubes is an unwanted pregnancy. National attorneys provide more information on website about the FDA Essure warning.

It is then that MadrisTomes found that the FDA and Bayer had underestimated the number of fetal deaths as being only 5 when she uncovered a couple of shortcomings to the FDA's search methodology. First was the fact that the FDA only searched the subject lines of the adverse event database for the term "fetal death" and did not search the entire content of the complaint. Secondly. other descriptive terms such as atopic pregnancy and miscarriage were omitted from the search. When these two items were made more inclusive, over 300 women were found to have reported unwanted pregnancies, miscarriages, stillborn children and fetal deaths. Ms Tomes was quoted in the New York Times when asked what first triggered her Essure suspicions, "With side effects ranging from hair loss and tooth loss to chronic pain, severe bleeding, miscarriages, and even death, the benefit-risk profile touted by Bayer simply didn't jibe with the data that was pouring into the F.D.A. from both patients and physicians."

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OnderLaw, LLC 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. OnderLaw 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.