ESSURE Adverse Event — Injury (MDR 2951250-2020-05757)
ESSURE Adverse Event — Injury (MDR 2951250-2020-05757) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ESSURE; Generic name: TRANSCERVICAL CONTRACEPTIVE TUBAL OCCLUSION DEVICE; Manufacturer: BAYER PHARMA AG.
| Device | ESSURE |
|---|---|
| Generic name | TRANSCERVICAL CONTRACEPTIVE TUBAL OCCLUSION DEVICE |
| Manufacturer | BAYER PHARMA AG |
| Report number | 2951250-2020-05757 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | CONSUMER, OTHER |
| Narrative | THIS SPONTANEOUS CASE WAS REPORTED BY A LAWYER AND DESCRIBES THE OCCURRENCE OF DYSMENORRHOEA ('MY PERIODS CAUSING CRAMPS SO BAD THE PAIN WOULD SHOOT DOWN MY LEGS AND CAUSE ME TO PASS OUT') IN A 30-YEAR-OLD FEMALE PATIENT WHO HAD ESSURE INSERTED. THE PATIENT'S MEDICAL HISTORY INCLUDED CERVICAL CANCER AND UTERINE CANCER. ON AN UNKNOWN DATE, THE PATIENT HAD ESSURE INSERTED. ON AN UNKNOWN DATE, THE PA |
| Source | openFDA MAUDE (device adverse events) |
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