Mirena IUD issues

The Dangers of Mirena IUDs – Could you be at Risk?

The Mirena IUD is a device that has been implanted in thousands of women as a form of birth control. This device is manufactured by Bayer Pharmaceuticals, and works by emitting a hormone that helps prevent pregnancy. The IUD was designed to last for up to five years without needing to be replaced. It has recently come under attack for causing a number of complications that could sometimes result in permanent injuries.

The problem with the Mirena IUD is that it sometimes migrates through the uterine wall and then enters other parts of a woman’s body. When this occurs, there could be severe complications that may include:

• Perforation of the Uterus or Cervix
• Device migration resulting in Laparoscopic surgery
• Ectopic or intrauterine pregnancies
• Pelvic inflammatory disease

In addition to these complications, IUD devices that migrate could cause the perforation of other organs such as the spleen, liver or pancreas. Surgery is required to remove this device if it becomes dislodged. In some cases, the device could cause serious trauma to the uterus, thereby making it difficult for a woman to conceive even after it is removed.

FDA Warnings

There is some evidence that shows Bayer received warnings from the FDA about the possible complications involved with Mirena IUDs. This agency claimed that Bayer misstated the product’s effectiveness and failed to provide patients with information about the possible risks. Although there have been more than 45,000 reports of complications from users and numerous lawsuits have been filed, Bayer has yet to formally recall this birth control device.

Increased Risk

There is an increased risk of Mirena injuries among women who have an unusual-shaped anatomy or previous trauma to the uterus. When the device is placed shortly after childbirth, the odds are also greater than it will migrate or tear the uterus.

Women who have been implanted with the Mirena IUD may want to speak to their doctor about having it removed. Those who have suffered an injury after the insertion of this device may want to contact us to protect their rights.