Does FEXOFENADINE OTC Cause Product quality issue? 75 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 75 reports of Product quality issue have been filed in association with FEXOFENADINE OTC. This represents 41.0% of all adverse event reports for FEXOFENADINE OTC.
75
Reports of Product quality issue with FEXOFENADINE OTC
41.0%
of all FEXOFENADINE OTC reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From FEXOFENADINE OTC?
Of the 75 reports.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FEXOFENADINE OTC. However, 75 reports have been filed with the FAERS database.
What Other Side Effects Does FEXOFENADINE OTC Cause?
Drug ineffective (70)
No adverse event (30)
Extra dose administered (29)
Dizziness (8)
Expired product administered (8)
Headache (8)
Somnolence (7)
Wrong technique in drug usage process (6)
Dyspnoea (5)
Insomnia (5)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which FEXOFENADINE OTC Alternatives Have Lower Product quality issue Risk?
FEXOFENADINE OTC vs FEXOFENADINE\FEXOFENADINE
FEXOFENADINE OTC vs FEXOFENADINE\PSEUDOEPHEDRINE
FEXOFENADINE OTC vs FEZOLINETANT
FEXOFENADINE OTC vs FIBRINOGEN HUMAN
FEXOFENADINE OTC vs FIBRINOGEN HUMAN\HUMAN THROMBIN