Does COPPER Cause Device breakage? 9,201 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9,201 reports of Device breakage have been filed in association with COPPER (Cuprum metallicum 7116). This represents 24.0% of all adverse event reports for COPPER.
9,201
Reports of Device breakage with COPPER
24.0%
of all COPPER reports
0
Deaths
182
Hospitalizations
How Dangerous Is Device breakage From COPPER?
Of the 9,201 reports, 182 (2.0%) required hospitalization, and 7 (0.1%) were considered life-threatening.
Is Device breakage Listed in the Official Label?
Yes, Device breakage is listed as a known adverse reaction in the official FDA drug label for COPPER.
What Other Side Effects Does COPPER Cause?
Device expulsion (11,141)
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)
Anxiety (2,445)
What Other Drugs Cause Device breakage?
SOMATROPIN (7,761)
ETONOGESTREL (4,140)
LEVONORGESTREL (2,726)
ETHINYL ESTRADIOL\ETONOGESTREL (741)
CARBIDOPA\LEVODOPA (634)
TREPROSTINIL (396)
ADALIMUMAB (375)
ALBUTEROL (256)
EPOPROSTENOL (240)
INSULIN GLARGINE (237)
Which COPPER Alternatives Have Lower Device breakage Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE