Does AZELASTINE Cause Product dose omission issue? 259 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 259 reports of Product dose omission issue have been filed in association with AZELASTINE (Azelastine Hydrochloride). This represents 4.4% of all adverse event reports for AZELASTINE.
259
Reports of Product dose omission issue with AZELASTINE
4.4%
of all AZELASTINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From AZELASTINE?
Of the 259 reports.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZELASTINE. However, 259 reports have been filed with the FAERS database.
What Other Side Effects Does AZELASTINE Cause?
Treatment failure (1,873)
Drug ineffective (944)
No adverse event (275)
Product delivery mechanism issue (267)
Dysgeusia (246)
Headache (205)
Nasal discomfort (205)
Somnolence (185)
Sneezing (184)
Dizziness (148)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which AZELASTINE Alternatives Have Lower Product dose omission issue Risk?
AZELASTINE vs AZELASTINE\FLUTICASONE
AZELASTINE vs AZELNIDIPINE
AZELASTINE vs AZILECT
AZELASTINE vs AZILSARTAN KAMEDOXOMIL
AZELASTINE vs AZILSARTAN KAMEDOXOMIL\CHLORTHALIDONE