Does CODEINE\GUAIFENESIN Cause Product prescribing issue? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product prescribing issue have been filed in association with CODEINE\GUAIFENESIN. This represents 1.1% of all adverse event reports for CODEINE\GUAIFENESIN.
11
Reports of Product prescribing issue with CODEINE\GUAIFENESIN
1.1%
of all CODEINE\GUAIFENESIN reports
2
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing issue From CODEINE\GUAIFENESIN?
Of the 11 reports, 2 (18.2%) resulted in death.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CODEINE\GUAIFENESIN. However, 11 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which CODEINE\GUAIFENESIN Alternatives Have Lower Product prescribing 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