Does FEXOFENADINE Cause Expired product administered? 379 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 379 reports of Expired product administered have been filed in association with FEXOFENADINE (Fexofenadine HCl). This represents 1.8% of all adverse event reports for FEXOFENADINE.
379
Reports of Expired product administered with FEXOFENADINE
1.8%
of all FEXOFENADINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Expired product administered From FEXOFENADINE?
Of the 379 reports, 3 (0.8%) required hospitalization, and 1 (0.3%) were considered life-threatening.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FEXOFENADINE. However, 379 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which FEXOFENADINE Alternatives Have Lower Expired product administered Risk?
FEXOFENADINE vs FEXOFENADINE OTC
FEXOFENADINE vs FEXOFENADINE\FEXOFENADINE
FEXOFENADINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FEXOFENADINE vs FEZOLINETANT
FEXOFENADINE vs FIBRINOGEN HUMAN