Safety Alert for Mirena

According to Health Ministry (Panama), this safety alert involved a device in Panama that was produced by Bayer Pharma AG.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2016-06-16
  • Event Date Posted
    2016-07-12
  • Event Country
  • Event Source
    HMP
  • Event Source URL
  • Notes / Alerts
    Panamanian data is current through January 2019. All of the data comes from the Health Ministry (Panama), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Panama.
  • Extra notes in the data
  • Reason
    The australian regulatory medicines agency, the therapeutic goods administration (tga), has announced that intrauterine device (iud) information containing 52 mg of levonorgestrel (mirena®) will be reviewed to include information regarding an increased risk of uterine perforation for breastfeeding women during the first 36 weeks after delivery. while it is known that uterine perforation is a rare adverse event associated with the use of intrauterine contraceptive devices, a recent european study has found that the risk of uterine perforation increases in nursing women and during the first 36 weeks after delivery.

Device

  • Model / Serial
  • Product Description
    Mirena® is an intrauterine device that contains levonorgestrel, a progestagen with antiestrogenic activity, that releases 20 µg of the hormone every 24 hours directly into the intrauterine cavity.
  • Manufacturer

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    HMP