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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does AZELASTINE Cause Condition aggravated? 79 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Condition aggravated have been filed in association with AZELASTINE (Azelastine Hydrochloride). This represents 1.3% of all adverse event reports for AZELASTINE.

79
Reports of Condition aggravated with AZELASTINE
1.3%
of all AZELASTINE reports
0
Deaths
6
Hospitalizations

How Dangerous Is Condition aggravated From AZELASTINE?

Of the 79 reports, 6 (7.6%) required hospitalization, and 1 (1.3%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZELASTINE. However, 79 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which AZELASTINE Alternatives Have Lower Condition aggravated Risk?

AZELASTINE vs AZELASTINE\FLUTICASONE AZELASTINE vs AZELNIDIPINE AZELASTINE vs AZILECT AZELASTINE vs AZILSARTAN KAMEDOXOMIL AZELASTINE vs AZILSARTAN KAMEDOXOMIL\CHLORTHALIDONE

Related Pages

AZELASTINE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated AZELASTINE Demographics