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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 CODEINE\GUAIFENESIN Cause Product use issue? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product use issue have been filed in association with CODEINE\GUAIFENESIN. This represents 0.9% of all adverse event reports for CODEINE\GUAIFENESIN.

9
Reports of Product use issue with CODEINE\GUAIFENESIN
0.9%
of all CODEINE\GUAIFENESIN reports
9
Deaths
0
Hospitalizations

How Dangerous Is Product use issue From CODEINE\GUAIFENESIN?

Of the 9 reports, 9 (100.0%) resulted in death.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CODEINE\GUAIFENESIN. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does CODEINE\GUAIFENESIN Cause?

Dependence (816) Overdose (501) Death (115) Drug ineffective (53) Pain (51) Drug hypersensitivity (47) Rash (45) Nausea (42) Drug intolerance (41) Psoriasis (40)

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)

Which CODEINE\GUAIFENESIN Alternatives Have Lower Product use issue Risk?

CODEINE\GUAIFENESIN vs CODEINE\IBUPROFEN CODEINE\GUAIFENESIN vs CODEINE\PROMETHAZINE CODEINE\GUAIFENESIN vs COLCHICINE CODEINE\GUAIFENESIN vs COLCHICINE\DICYCLOMINE CODEINE\GUAIFENESIN vs COLCHICINE\OPIUM\TIEMONIUM METHYLSULFATE

Related Pages

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