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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 ACETAMINOPHEN\CAFFEINE\GUAIFENESIN Cause Product use issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use issue have been filed in association with ACETAMINOPHEN\CAFFEINE\GUAIFENESIN. This represents 13.2% of all adverse event reports for ACETAMINOPHEN\CAFFEINE\GUAIFENESIN.

5
Reports of Product use issue with ACETAMINOPHEN\CAFFEINE\GUAIFENESIN
13.2%
of all ACETAMINOPHEN\CAFFEINE\GUAIFENESIN reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product use issue From ACETAMINOPHEN\CAFFEINE\GUAIFENESIN?

Of the 5 reports, 5 (100.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ACETAMINOPHEN\CAFFEINE\GUAIFENESIN. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does ACETAMINOPHEN\CAFFEINE\GUAIFENESIN Cause?

Suicide attempt (27) Intentional overdose (23) Intentional product misuse (7) Dysarthria (5) Nausea (5) Overdose (5) Somnolence (5) Vertigo (5)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

ACETAMINOPHEN\CAFFEINE\GUAIFENESIN Full Profile All Product use issue Reports All Drugs Causing Product use issue ACETAMINOPHEN\CAFFEINE\GUAIFENESIN Demographics