Does FEXOFENADINE Cause Condition aggravated? 375 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 375 reports of Condition aggravated have been filed in association with FEXOFENADINE (Fexofenadine HCl). This represents 1.8% of all adverse event reports for FEXOFENADINE.
375
Reports of Condition aggravated with FEXOFENADINE
1.8%
of all FEXOFENADINE reports
2
Deaths
36
Hospitalizations
How Dangerous Is Condition aggravated From FEXOFENADINE?
Of the 375 reports, 2 (0.5%) resulted in death, 36 (9.6%) required hospitalization, and 7 (1.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FEXOFENADINE. However, 375 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which FEXOFENADINE Alternatives Have Lower Condition aggravated Risk?
FEXOFENADINE vs FEXOFENADINE OTC
FEXOFENADINE vs FEXOFENADINE\FEXOFENADINE
FEXOFENADINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FEXOFENADINE vs FEZOLINETANT
FEXOFENADINE vs FIBRINOGEN HUMAN