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Women Complain About Essures Adverse Side Effects

Social media outlet Facebook provides a forum for women suffering from the side effects of Bayers Essure birth control device

Tuesday, November 7, 2017 - Over 35000 members of the Facebook group Essure Problems, many of whom are suffering from the side effects of Essure are furious that the FDA has not done more to remove Essure birth control devices from the US market as health regulators have done elsewhere in the world. In late September 2017, German Pharmaceutical giant Bayer, maker of Essure, announced that they had taken the birth control device off of the market in all countries except the United States due to commercial reasons not related to product quality or safety concerns. Bayer spokesmen have said that the company will not seek to renew its Essure trademark throughout the Europen Union. Members of the United States Congress are meeting soon to question why more has not been done by the FDA given the thousands of complaints from women using the device and the company's own removal of the lucrative product from the European market.

The adverse side effects of the Essure birth control coil that full-blown in a woman's fallopian tubes include abnormal monthly bleeding, chronic fatigue, allergies and autoimmune issues. There have been incidences where the device has migrated and perforated other organs causing infection. The nickel/titanium plating of the device has also caused adverse reactions in those with Nickel sensitivities. Other women wanting the device removed have been forced to undergo a radical hysterectomy to remove the device as scar tissue has made simple, non-surgical removal of the device impossible.

One women reported on the Facebook Essure page that the pain she suffered when the device was inserted was worse than going through labor. She was unable to go back to work and lost her job because of the inability to walk due to the pain. For two weeks the woman experienced enormous blood loss that required 5 overnight strength pads per day, abdominal swelling, migraine headaches, a feeling of her ovaries exploding, and constant fatigue that could not be alleviated by sleep or rest.

Another woman writes: "I was 26 (when Essure was implanted) and by the time I was 28 I was diagnosed with full blown menopause and suffer from pelvic pain, abdominal bloating (look 3 months pregnant), migraines, severe panic disorder, varicose veins in my legs, twitching like pain in my legs, chest pains, and so much more."

The complaints of women who use Essure continue. "I had an Essure placed in 2009. I started to notice changes in my body a few years later like, weight gain, excessive bleeding during my cycle and between time, extreme pain in my lower back, stomach, and pelvic area, to the point I couldn't walk sometime, constant nausea and fatigue, loss of hair and really bad allergic reactions I couldn't explain. The bleeding and pain got so bad I had to have a total hysterectomy on 8/16/17."

After more than 20,000 complaints of Essure problems submitted to the FDA to date, there is plenty of reason that thousands of Essure complications lawsuits have now been filed.

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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.