Does COPPER Cause Device dislocation? 6,955 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,955 reports of Device dislocation have been filed in association with COPPER (Cuprum metallicum 7116). This represents 18.2% of all adverse event reports for COPPER.
6,955
Reports of Device dislocation with COPPER
18.2%
of all COPPER reports
0
Deaths
90
Hospitalizations
How Dangerous Is Device dislocation From COPPER?
Of the 6,955 reports, 90 (1.3%) required hospitalization, and 7 (0.1%) were considered life-threatening.
Is Device dislocation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 6,955 reports have been filed with the FAERS database.
What Other Side Effects Does COPPER Cause?
Device expulsion (11,141)
Device breakage (9,201)
Complication of device removal (7,895)
Foreign body in reproductive tract (7,050)
Complication of device insertion (6,078)
Pain (5,118)
Reproductive complication associated with device (3,654)
Embedded device (3,425)
Injury associated with device (2,895)
Anxiety (2,445)
What Other Drugs Cause Device dislocation?
LEVONORGESTREL (13,757)
CARBIDOPA\LEVODOPA (2,937)
ETONOGESTREL (2,909)
TREPROSTINIL (1,626)
MIRENA (677)
BACLOFEN (492)
PARAGARD 380A (479)
ADALIMUMAB (372)
EPOPROSTENOL (358)
DEXAMETHASONE (290)
Which COPPER Alternatives Have Lower Device dislocation Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE