Does COPPER Cause Device issue? 819 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 819 reports of Device issue have been filed in association with COPPER (Cuprum metallicum 7116). This represents 2.1% of all adverse event reports for COPPER.
819
Reports of Device issue with COPPER
2.1%
of all COPPER reports
0
Deaths
10
Hospitalizations
How Dangerous Is Device issue From COPPER?
Of the 819 reports, 10 (1.2%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 819 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which COPPER Alternatives Have Lower Device issue Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE