Does COPPER Cause Device deployment issue? 768 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 768 reports of Device deployment issue have been filed in association with COPPER (Cuprum metallicum 7116). This represents 2.0% of all adverse event reports for COPPER.
768
Reports of Device deployment issue with COPPER
2.0%
of all COPPER reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device deployment issue From COPPER?
Of the 768 reports, 1 (0.1%) required hospitalization.
Is Device deployment issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 768 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 deployment issue?
ETONOGESTREL (3,621)
GOLIMUMAB (1,265)
GUSELKUMAB (778)
LEVONORGESTREL (718)
USTEKINUMAB (639)
SUMATRIPTAN (292)
PEGFILGRASTIM (163)
ABATACEPT (131)
SOMATROPIN (130)
CARBIDOPA\LEVODOPA (88)
Which COPPER Alternatives Have Lower Device deployment issue Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE