Does AZELASTINE Cause Device issue? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Device issue have been filed in association with AZELASTINE (Azelastine Hydrochloride). This represents 1.2% of all adverse event reports for AZELASTINE.
70
Reports of Device issue with AZELASTINE
1.2%
of all AZELASTINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device issue From AZELASTINE?
Of the 70 reports.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AZELASTINE. However, 70 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 Device issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which AZELASTINE Alternatives Have Lower Device issue Risk?
AZELASTINE vs AZELASTINE\FLUTICASONE
AZELASTINE vs AZELNIDIPINE
AZELASTINE vs AZILECT
AZELASTINE vs AZILSARTAN KAMEDOXOMIL
AZELASTINE vs AZILSARTAN KAMEDOXOMIL\CHLORTHALIDONE