Does AZELASTINE\FLUTICASONE Cause Product dose omission issue? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Product dose omission issue have been filed in association with AZELASTINE\FLUTICASONE. This represents 5.5% of all adverse event reports for AZELASTINE\FLUTICASONE.
70
Reports of Product dose omission issue with AZELASTINE\FLUTICASONE
5.5%
of all AZELASTINE\FLUTICASONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product dose omission issue From AZELASTINE\FLUTICASONE?
Of the 70 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\FLUTICASONE. However, 70 reports have been filed with the FAERS database.
What Other Side Effects Does AZELASTINE\FLUTICASONE Cause?
Drug ineffective (148)
Asthma (101)
Dyspnoea (101)
Headache (92)
Dysgeusia (91)
Epistaxis (82)
Off label use (80)
Pneumonia (77)
Product delivery mechanism issue (68)
Cough (65)
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\FLUTICASONE Alternatives Have Lower Product dose omission issue Risk?
AZELASTINE\FLUTICASONE vs AZELNIDIPINE
AZELASTINE\FLUTICASONE vs AZILECT
AZELASTINE\FLUTICASONE vs AZILSARTAN KAMEDOXOMIL
AZELASTINE\FLUTICASONE vs AZILSARTAN KAMEDOXOMIL\CHLORTHALIDONE
AZELASTINE\FLUTICASONE vs AZITHROMYCIN