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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 Product packaging quantity issue? 28 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product packaging quantity issue have been filed in association with AZELASTINE (Azelastine Hydrochloride). This represents 0.5% of all adverse event reports for AZELASTINE.

28
Reports of Product packaging quantity issue with AZELASTINE
0.5%
of all AZELASTINE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product packaging quantity issue From AZELASTINE?

Of the 28 reports.

Is Product packaging quantity issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for AZELASTINE. However, 28 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 Product packaging quantity issue?

LEUPROLIDE (523) ALBUTEROL (431) BUDESONIDE\FORMOTEROL (301) FENTANYL (286) BUPRENORPHINE (225) CYCLOSPORINE (206) ESTRADIOL (201) BIMATOPROST (177) RIVAROXABAN (174) EXENATIDE (154)

Which AZELASTINE Alternatives Have Lower Product packaging quantity issue 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 Product packaging quantity issue Reports All Drugs Causing Product packaging quantity issue AZELASTINE Demographics