Does COPPER Cause Intentional product use issue? 76 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 76 reports of Intentional product use issue have been filed in association with COPPER (Cuprum metallicum 7116). This represents 0.2% of all adverse event reports for COPPER.
76
Reports of Intentional product use issue with COPPER
0.2%
of all COPPER reports
0
Deaths
1
Hospitalizations
How Dangerous Is Intentional product use issue From COPPER?
Of the 76 reports, 1 (1.3%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 76 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which COPPER Alternatives Have Lower Intentional product use issue Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE