Does FEXOFENADINE Cause Incorrect product administration duration? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Incorrect product administration duration have been filed in association with FEXOFENADINE (Fexofenadine HCl). This represents 0.1% of all adverse event reports for FEXOFENADINE.
23
Reports of Incorrect product administration duration with FEXOFENADINE
0.1%
of all FEXOFENADINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From FEXOFENADINE?
Of the 23 reports, 1 (4.3%) 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 FEXOFENADINE. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does FEXOFENADINE Cause?
Drug ineffective (7,188)
Extra dose administered (1,413)
No adverse event (1,187)
Somnolence (961)
Therapeutic response decreased (742)
Headache (704)
Insomnia (642)
Feeling abnormal (617)
Dizziness (613)
Product quality issue (488)
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 FEXOFENADINE Alternatives Have Lower Incorrect product administration duration Risk?
FEXOFENADINE vs FEXOFENADINE OTC
FEXOFENADINE vs FEXOFENADINE\FEXOFENADINE
FEXOFENADINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FEXOFENADINE vs FEZOLINETANT
FEXOFENADINE vs FIBRINOGEN HUMAN