SAN DIEGO – Since 2004, almost 850 women and doctors have filed Adverse Event Reports with the Food and Drug Administration (FDA) about Essure birth control.
They detail extreme symptoms – from women experiencing excess bleeding, rashes and bloating to women who were forced to have their reproductive organs removed.
Now, Team 10 learned of a new Adverse Event Report filed with the FDA just weeks ago regarding Essure. It details a woman’s death after she was admitted to the hospital for abdominal pain. She had the Essure coils implanted this year, but it has not been determined what caused her death.