Does GUAIFENESIN Cause Incorrect product administration duration? 282 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 282 reports of Incorrect product administration duration have been filed in association with GUAIFENESIN (Guaifenesin and Pseudoephedrine HCl). This represents 3.5% of all adverse event reports for GUAIFENESIN.
282
Reports of Incorrect product administration duration with GUAIFENESIN
3.5%
of all GUAIFENESIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From GUAIFENESIN?
Of the 282 reports, 1 (0.4%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GUAIFENESIN. However, 282 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)
Product use issue (290)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which GUAIFENESIN Alternatives Have Lower Incorrect product administration duration Risk?
GUAIFENESIN vs GUAIFENESIN\HYDROCODONE
GUAIFENESIN vs GUAIFENESIN\PSEUDOEPHEDRINE
GUAIFENESIN vs GUANFACINE
GUAIFENESIN vs GUSELKUMAB
GUAIFENESIN vs HAIR KERATIN AMINO ACIDS GOLD COMPLEX