Does GUAIFENESIN Cause Product use issue? 290 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 290 reports of Product use issue have been filed in association with GUAIFENESIN (Guaifenesin and Pseudoephedrine HCl). This represents 3.6% of all adverse event reports for GUAIFENESIN.
290
Reports of Product use issue with GUAIFENESIN
3.6%
of all GUAIFENESIN reports
4
Deaths
5
Hospitalizations
How Dangerous Is Product use issue From GUAIFENESIN?
Of the 290 reports, 4 (1.4%) resulted in death, 5 (1.7%) 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 GUAIFENESIN. However, 290 reports have been filed with the FAERS database.
What Other Side Effects Does GUAIFENESIN Cause?
Drug ineffective (1,583)
Incorrect drug administration duration (490)
No adverse event (462)
Product use in unapproved indication (451)
Dizziness (423)
Accidental overdose (396)
Diarrhoea (359)
Nausea (344)
Headache (308)
Incorrect product administration duration (282)
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 GUAIFENESIN Alternatives Have Lower Product use issue Risk?
GUAIFENESIN vs GUAIFENESIN\HYDROCODONE
GUAIFENESIN vs GUAIFENESIN\PSEUDOEPHEDRINE
GUAIFENESIN vs GUANFACINE
GUAIFENESIN vs GUSELKUMAB
GUAIFENESIN vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX