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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 Presyncope? 126 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 126 reports of Presyncope have been filed in association with COPPER (Cuprum metallicum 7116). This represents 0.3% of all adverse event reports for COPPER.

126
Reports of Presyncope with COPPER
0.3%
of all COPPER reports
0
Deaths
1
Hospitalizations

How Dangerous Is Presyncope From COPPER?

Of the 126 reports, 1 (0.8%) required hospitalization, and 1 (0.8%) were considered life-threatening.

Is Presyncope Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for COPPER. However, 126 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 Presyncope?

TREPROSTINIL (585) BISOPROLOL (485) LEVONORGESTREL (429) ADALIMUMAB (420) AMBRISENTAN (407) ASPIRIN (370) TAMSULOSIN (361) FUROSEMIDE (348) SERTRALINE (337) ETANERCEPT (334)

Which COPPER Alternatives Have Lower Presyncope 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 Presyncope Reports All Drugs Causing Presyncope COPPER Demographics