DID YOU SUFFER ADVERSE SIDE EFFECTS AFTER RECEIVING THE NON-SURGICAL PERMANENT BIRTH CONTROL DEVICE ESSURE®?
The FDA has received thousands of complaints from women who suffered serious complications after receiving the non-surgical permanent birth control device Essure®, manufactured by Bayer. Some claim that Bayer knew about the adverse side effects, but concealed them from the public.
The nationwide trial lawyers at Bailey & Galyen are currently investigating Essure® injury claims. If you or a loved one was injured, we invite you to contact us to discuss your potential financial recovery.
SIDE EFFECTS
Reported side effects range in severity from bloating to miscarriage.
- Bloating
- Excessive Bleeding
- Rashes
- Chronic Pain
- Sharp Pelvic Pain
- Miscarriage
- Ectopic Pregnancy
Some women have had to undergo hysterectomy and hospitalization due to damage caused by the Essure® device.
ADVERSE EVENTS ASSOCIATED WITH THE ESSURE® DEVICE
Some doctors have reported various adverse events associated with the Essure® device, including:
- Coils breaking off the device
- Coils migrating from the fallopian tube
- Coils puncturing the fallopian tube
Many women who experienced these adverse events after receiving the Essure® device are still living with pain, even after receiving a hysterectomy or other medical treatment.
