Bayer's IUD Issues

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When health devices are sold in the United States, buyers feel secure utilizing them, as they understand the product - whether a prescription drug or medical product, has been thoroughly subjected to testing for safety and effectiveness. Conversely, it appears that the race to profit from new products by getting them to market may make long-term problems go undetected until the device is in the marketplace for awhile.

How else can you address the stories about failures having an effect on consumers who used a Bayer Pharmaceutical's Mirena IUD for contraception? The following illustrations of women affected by Bayer Pharmaceutical's Mirena IUD unwanted effects lend credibility to the charge that products are not being exhaustively tested before they are released to the public. Names have been altered.

Sara's Tale

Sara had a Bayer Pharmaceuticals Mirena IUD implanted at her doctors's office. Since a physician carried out the surgery, she assumed it was secure and that she'd taken needed precautions. She kept the device for 6 months, after which she and her husband decided to start a family. She went in to have the device removed. Even when the device was removed, she had a tough time getting pregnant. In an effort to increase her odds, she began utilizing ovulation drugs.

Even though there are many troubles connected to Mirena IUD, two of the most widespread are ectopic pregnancy and infertility. These worries were not explained to either Sara or her medical doctor. If she had known the greater risk, she never would have picked this sort of contraception device. She was troubled to find out that her choice would likely have an impact on her wish to have kids. She is now suing Bayer.

How a Mirena IUD Ripped Through a Uterus and Caused Kidney Failure

In 2011, Alexa also had a Mirena IUD implanted. After her implantation, Alexa's device dislodged and migrated through her body, ripping her uterus in the process. It then integrated itself in a different section of her body, causing kidney malfunction that nearly caused her to die. Now, Alexa is in near constant limited mobility, neck soreness, cramping, stomach issues, and a heavier period. Alexa is suing Bayer.

Mirena IUD

Mirena is a form of birth control which works by releasing hormones into a female's body. The product is plastic and must be inserted into the woman's vagina by a doctor. The hormone is released in a dose of 14 -20 mcg everyday. The job of the hormone is to weaken the uterus lining and strengthen cervical mucus to prevent sperm cells from reaching an egg. At the same time, the hormone prevents a woman's body from releasing an egg.

In 2009, the United States FDA additionally approved the Mirena IUD for the treatment of heavy menstrual bleeding.

Any time a patient decides she wants to have children, the device is taken out. From the moment that occurs, the ability to become pregnant returns, as reported by Bayer. the IUD is a long-term birth control solution and will last approximately five years. The item packaging implies that this device is to be used by women who have at least one baby. Why? The reason it is indicated for use in patients who already have a baby is that the company is aware that negative outcome of making use of Bayer's Mirena IUD is that it can produce fertility problems in patients. In the face of the known side effects, Bayer continues to sell the as a secure form of contraception that is absolutely reversible. No mention is made of the possible side effect of infertility.

The Risks and Difficulties Associated With Bayer Pharmaceuticals Mirena IUD

The Food and Drug Administration has logged fifty thousand complaints of serious complications regarding the insertion of the company's IUD.

These issues include: contamination, uterine wall embedding, pelvic inflammatory disease, hemorrhaging, uterine wall damage, ectopic pregnancy, perforation of the cervix, migration throughout the mid-section, sterility, irritation.

It is not uncommon for a woman to have surgery so as to remove the Mirena IUD or mend the harm it caused. One out of 1,000 patients may experience extreme complications according to the company.

Females who have encountered troubles as a result of making use of the Mirena IUD are filing lawsuits against the company for their soreness and distress.

Bayer and American Food and Drug Administration

The FDA issued a warning to Bayer in 2010. This letter condemned their advertising campaign as deceiving. The FDA ordered Bayer to fix its package label to include a more comprehensive warning, stating that Bayer was bolstering the many benefits of the product were not accurately portraying the side effects.This word of caution lists comprehensive side effects that can be encountered by making use of the device including: embedment of device in other parts of the body, congenital anomalies, ovarian nodules, expulsion, tearing of the uterus, breast cancer.

Mirena Lawsuit Status

Women who believeBayer knew of the Mirena IUD side effects and yet failed to warn patients are suingthe manufacturer. If they had known of the side effects, they may not to use the product.

Right now,46 federal lawsuits have been combined into a Multidistrict litigation, called an MDL. This case is designated MDL 2434 and titled In Re: Bayer Pharmaceuticals Mirena IUD Liability Litigation. In addition, there are 113 Mirena cases making their way through state court in New Jersey and a handful of cases in each of the following states; New York, California, Mississippi and Missouri.

What to do if you've been affected by a product

If you've suffered side effects from a Bayer Pharmaceuticals Mirena IUD or know of someone who has, it is vital to contact a legal representative who specializes in such matters. Many attorneys will offer a free case evaluation.

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