Does GUAIFENESIN Cause Product use in unapproved indication? 451 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 451 reports of Product use in unapproved indication have been filed in association with GUAIFENESIN (Guaifenesin and Pseudoephedrine HCl). This represents 5.6% of all adverse event reports for GUAIFENESIN.
451
Reports of Product use in unapproved indication with GUAIFENESIN
5.6%
of all GUAIFENESIN reports
5
Deaths
6
Hospitalizations
How Dangerous Is Product use in unapproved indication From GUAIFENESIN?
Of the 451 reports, 5 (1.1%) resulted in death, 6 (1.3%) required hospitalization, and 1 (0.2%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUAIFENESIN. However, 451 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)
Dizziness (423)
Accidental overdose (396)
Diarrhoea (359)
Nausea (344)
Headache (308)
Product use issue (290)
Incorrect product administration duration (282)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which GUAIFENESIN Alternatives Have Lower Product use in unapproved indication Risk?
GUAIFENESIN vs GUAIFENESIN\HYDROCODONE
GUAIFENESIN vs GUAIFENESIN\PSEUDOEPHEDRINE
GUAIFENESIN vs GUANFACINE
GUAIFENESIN vs GUSELKUMAB
GUAIFENESIN vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX