COPPER for Intrauterine contraception: Side Effects & Safety Data
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There are 11 adverse event reports in the FDA FAERS database where COPPER was used for Intrauterine contraception.
Most Reported Side Effects for COPPER
| Side Effect | Reports | % | Deaths | Hosp. |
|---|---|---|---|---|
| Device expulsion | 11,141 | 29.1% | 0 | 38 |
| Device breakage | 9,201 | 24.0% | 0 | 182 |
| Complication of device removal | 7,895 | 20.6% | 0 | 142 |
| Foreign body in reproductive tract | 7,050 | 18.4% | 0 | 87 |
| Device dislocation | 6,955 | 18.2% | 0 | 90 |
| Complication of device insertion | 6,078 | 15.9% | 0 | 2 |
| Pain | 5,118 | 13.4% | 0 | 88 |
| Reproductive complication associated with device | 3,654 | 9.6% | 0 | 35 |
| Embedded device | 3,425 | 9.0% | 0 | 111 |
| Injury associated with device | 2,895 | 7.6% | 0 | 8 |
| Anxiety | 2,445 | 6.4% | 3 | 43 |
| Muscle spasms | 2,049 | 5.4% | 0 | 35 |
| Pelvic pain | 1,963 | 5.1% | 0 | 41 |
| Off label use | 1,941 | 5.1% | 0 | 12 |
| Emotional distress | 1,764 | 4.6% | 0 | 28 |
Other Indications for COPPER
Contraception (28,180)
Product used for unknown indication (6,756)
Post coital contraception (86)
Menstruation irregular (18)
Abnormal uterine bleeding (10)
Parenteral nutrition (5)