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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does COPPER Cause Embedded device? 3,425 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 3,425 reports of Embedded device have been filed in association with COPPER (Cuprum metallicum 7116). This represents 9.0% of all adverse event reports for COPPER.

3,425
Reports of Embedded device with COPPER
9.0%
of all COPPER reports
0
Deaths
111
Hospitalizations

How Dangerous Is Embedded device From COPPER?

Of the 3,425 reports, 111 (3.2%) required hospitalization, and 6 (0.2%) were considered life-threatening.

Is Embedded device Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for COPPER. However, 3,425 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) Injury associated with device (2,895) Anxiety (2,445)

What Other Drugs Cause Embedded device?

LEVONORGESTREL (3,413) CARBIDOPA\LEVODOPA (736) MIRENA (159) PARAGARD 380A (107) ETONOGESTREL (30) UNSPECIFIED INGREDIENT (12) ADALIMUMAB (11) TREPROSTINIL (8)

Which COPPER Alternatives Have Lower Embedded device Risk?

COPPER vs CORDARONE COPPER vs CORICIDIN HBP COLD AND FLU COPPER vs CORTICOSTEROID NOS COPPER vs CORTICOTROPIN COPPER vs CORTISONE

Related Pages

COPPER Full Profile All Embedded device Reports All Drugs Causing Embedded device COPPER Demographics