Does FEXOFENADINE Cause Unevaluable event? 240 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 240 reports of Unevaluable event have been filed in association with FEXOFENADINE (Fexofenadine HCl). This represents 1.1% of all adverse event reports for FEXOFENADINE.
240
Reports of Unevaluable event with FEXOFENADINE
1.1%
of all FEXOFENADINE reports
1
Deaths
7
Hospitalizations
How Dangerous Is Unevaluable event From FEXOFENADINE?
Of the 240 reports, 1 (0.4%) resulted in death, 7 (2.9%) required hospitalization, and 1 (0.4%) were considered life-threatening.
Is Unevaluable event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FEXOFENADINE. However, 240 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 Unevaluable event?
ADALIMUMAB (4,242)
ETANERCEPT (3,902)
LENALIDOMIDE (3,331)
OXYCODONE (3,145)
AMBRISENTAN (2,336)
SODIUM OXYBATE (2,328)
CARBIDOPA\LEVODOPA (1,632)
DUPILUMAB (1,410)
MORPHINE (1,161)
ACETAMINOPHEN\HYDROCODONE (1,118)
Which FEXOFENADINE Alternatives Have Lower Unevaluable event Risk?
FEXOFENADINE vs FEXOFENADINE OTC
FEXOFENADINE vs FEXOFENADINE\FEXOFENADINE
FEXOFENADINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FEXOFENADINE vs FEZOLINETANT
FEXOFENADINE vs FIBRINOGEN HUMAN