Does AZELASTINE Cause Incorrect product administration duration? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Incorrect product administration duration have been filed in association with AZELASTINE (Azelastine Hydrochloride). This represents 0.1% of all adverse event reports for AZELASTINE.
6
Reports of Incorrect product administration duration with AZELASTINE
0.1%
of all AZELASTINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product administration duration From AZELASTINE?
Of the 6 reports.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZELASTINE. However, 6 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)
Product dose omission issue (259)
Dysgeusia (246)
Headache (205)
Nasal discomfort (205)
Somnolence (185)
Sneezing (184)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which AZELASTINE Alternatives Have Lower Incorrect product administration duration Risk?
AZELASTINE vs AZELASTINE\FLUTICASONE
AZELASTINE vs AZELNIDIPINE
AZELASTINE vs AZILECT
AZELASTINE vs AZILSARTAN KAMEDOXOMIL
AZELASTINE vs AZILSARTAN KAMEDOXOMIL\CHLORTHALIDONE