Essure birth control controversy: 5 Things You Should Know
#Cosmoread: Essure a permanent birth control implants, a strong warning that the potentially serious risks of the device will need to be labeled with the list, the Food and Drug Administration announced this week.
After the action the FDA, more than 5,000 reports of complications from the device for chronic pain, including bleeding and allergic reactions since the device was approved in 2002, here’s what you need to know about the controversy comes in.
Essure device and who gets what?
Essure, manufactured by Bayer, a permanent (irreversible) is a form of birth control, a woman who gets the device will be no longer able to become pregnant meaning. The women who do not want any more children is intended for. Studies have shown that if the device is implanted correctly, the possibility of pregnancy is less than 1 percent, the FDA said. Essure about 750,000 women have received since 2002, according to Bayer.
How does it work?
The traditional method of female sterilization, tubal ligation or as “having your tubes tied,” is not required to file a essure contrast to surgical incisions. Instead, a doctor implants can be inserted through the woman’s vagina, past the cervix and into the fallopian tubes. Over time, scar tissue builds up around the place, a barrier that prevents sperm from reaching the egg in the fallopian tube, making the FDA said.
Part of the device is made from a nickel-titanium alloy, a nickel allergy patients with rash, itching and hives device, including an allergic reaction may occur, Bayer said.
What are the complaints about it?
Essure FDA said it still considers “women seeking permanent birth control is an appropriate choice for the majority,” but the agency also said that some women may be at risk for serious problems. In the past 14 years, some women using essure constant pain, abnormal bleeding, allergies, and perforation of the uterus or fallopian tubes have reported.
What the FDA is doing?
FDA essure a new warning labels on some serious problems that have been reported by women using the device will need to describe. The agency is a “list” that doctors discuss with patients the risk to the device that you can use is developing. Check list will emphasize that patients so that doctors can check if the device is properly placed and the fallopian tubes are blocked to prevent pregnancy, “confirmation test” essure implanted after three months are needed to pass.
The FDA also required to conduct a study of essure Bayer unplanned pregnancy, pelvic pain and the risk of complications, observing and comparing those to the risk of tubal ligation.
There are other similar types of birth control?
No, Bayer said it does not require surgical incisions essure women that birth control is the only permanently.