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Essure Causes Hundreds of Adverse Side Effects

A comprehensive list of side effects from Essure Birth Control

Monday, June 18, 2018 - Women are reporting that physically speaking, the Essure birth control device has ruined their lives. The list of adverse side effects that women are experiencing is staggering, to say the least, and too many to list here. Over 35,000 women have been approved to join the tightly-controlled Essure Problems Facebook group where women are encouraged to share their stories and to alert others to avoid Essure at all costs. These Facebook Essure victims are functioning to alert others to the health risks of Essure since neither the government nor the company that makes the device will do so.

Essure is a soft, flexible birth control device that resembles the spring from a retractable ballpoint pen and made from a combination of Nickel-Titanium, Polyethylene (polyester), Stainless Steel, Platinum, Silver, and Tin. One Essure device is inserted into each Fallopian tube where the polyester fibers are intended to cause irritation in the underlying Fallopian tissue, creating scar tissue, and holding the device in place. Scar tissue also grows to block the Fallopian tube and prevent the sperm from reaching the egg. Women are advised to wait 3 months before having sex to ensure the device has taken hold. Essure has been on the market since 2002 and is approved by the US FDA for use by women age 21-45. Essure can be inserted in the comfort and convenience of a doctor's office and does not require anesthesia. No surgery is required. Essure was once sold to women as a temporary form of birth control, one that could be reversed when a woman wanted to try to become pregnant. Unforeseen adverse consequences of Essure have forced thousands of women to undergo surgery to have the device removed. Such surgery usually requires the removal of a part or all of a woman's reproductive organs, much like the hysterectomy that the patient was originally intending to avoid.

One of the more serious consequences of Essure is that the device doesn't always remain attached to the inner wall of the Fallopian tube like it is supposed to. Quite often the device breaks into multiple, sharp pieces and migrates to a woman's other reproductive organs such as the uterus and causes excruciating pain. Essure women report that the device has punctured the uterus and caused bleeding forcing the removal of the device. Such removal often fails without the complete removal of the uterus.

When the Essure device does remain in place, an unacceptably high number of women experience allergic and autoimmune issues due to having a reaction to the nickel plating of the device. As pertains to allergic reactions to Essure, the FDA reports that "typical symptoms may include rash, itching, and hives but may also include other symptoms not reported in the clinical trials such as chest pain, breathing difficulties and intestinal discomforts such as nausea, diarrhea or vomiting."

Thousands of Essure woman are consulting with Essure problems attorneys to see if they qualify to file a claim against the company and seek compensation for their medical expenses, lost wages, and pain and suffering.

Visit this link for even more side effects women have reported from the Essure Birth Control device: http://essureproblems.webs.com/side-effects-of-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.