Does COPPER Cause Complication of device removal? 7,895 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7,895 reports of Complication of device removal have been filed in association with COPPER (Cuprum metallicum 7116). This represents 20.6% of all adverse event reports for COPPER.
7,895
Reports of Complication of device removal with COPPER
20.6%
of all COPPER reports
0
Deaths
142
Hospitalizations
How Dangerous Is Complication of device removal From COPPER?
Of the 7,895 reports, 142 (1.8%) required hospitalization, and 8 (0.1%) were considered life-threatening.
Is Complication of device removal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 7,895 reports have been filed with the FAERS database.
What Other Side Effects Does COPPER Cause?
Device expulsion (11,141)
Device breakage (9,201)
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 Complication of device removal?
ETONOGESTREL (3,578)
LEVONORGESTREL (2,039)
MIRENA (44)
INTERFERON BETA-1A (37)
TREPROSTINIL (24)
IMPLANON (21)
ETHINYL ESTRADIOL\ETONOGESTREL (15)
UNSPECIFIED INGREDIENT (14)
BUPRENORPHINE (11)
DEVICE (11)
Which COPPER Alternatives Have Lower Complication of device removal Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE