Does COPPER Cause Complication of device insertion? 6,078 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6,078 reports of Complication of device insertion have been filed in association with COPPER (Cuprum metallicum 7116). This represents 15.9% of all adverse event reports for COPPER.
6,078
Reports of Complication of device insertion with COPPER
15.9%
of all COPPER reports
0
Deaths
2
Hospitalizations
How Dangerous Is Complication of device insertion From COPPER?
Of the 6,078 reports, 2 (0.0%) required hospitalization.
Is Complication of device insertion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 6,078 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)
Device dislocation (6,955)
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 Complication of device insertion?
LEVONORGESTREL (4,662)
ETONOGESTREL (3,234)
DEXAMETHASONE (168)
MIRENA (53)
CARBIDOPA\LEVODOPA (51)
DEVICE (50)
CHLORHEXIDINE\ISOPROPYL ALCOHOL (49)
PARAGARD 380A (46)
BIMATOPROST (33)
FLUOCINOLONE ACETONIDE (31)
Which COPPER Alternatives Have Lower Complication of device insertion Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE