Does COPPER Cause Device use issue? 1,318 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,318 reports of Device use issue have been filed in association with COPPER (Cuprum metallicum 7116). This represents 3.4% of all adverse event reports for COPPER.
1,318
Reports of Device use issue with COPPER
3.4%
of all COPPER reports
0
Deaths
20
Hospitalizations
How Dangerous Is Device use issue From COPPER?
Of the 1,318 reports, 20 (1.5%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 1,318 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)
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)
What Other Drugs Cause Device use issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
LEVODOPA (443)
Which COPPER Alternatives Have Lower Device use issue Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE