Does FEXOFENADINE Cause Intentional product misuse? 170 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 170 reports of Intentional product misuse have been filed in association with FEXOFENADINE (Fexofenadine HCl). This represents 0.8% of all adverse event reports for FEXOFENADINE.
170
Reports of Intentional product misuse with FEXOFENADINE
0.8%
of all FEXOFENADINE reports
1
Deaths
3
Hospitalizations
How Dangerous Is Intentional product misuse From FEXOFENADINE?
Of the 170 reports, 1 (0.6%) resulted in death, 3 (1.8%) required hospitalization, and 1 (0.6%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FEXOFENADINE. However, 170 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which FEXOFENADINE Alternatives Have Lower Intentional product misuse Risk?
FEXOFENADINE vs FEXOFENADINE OTC
FEXOFENADINE vs FEXOFENADINE\FEXOFENADINE
FEXOFENADINE vs FEXOFENADINE\PSEUDOEPHEDRINE
FEXOFENADINE vs FEZOLINETANT
FEXOFENADINE vs FIBRINOGEN HUMAN