Does FLUTICASONE Cause Product dose omission issue? 1,060 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,060 reports of Product dose omission issue have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 3.3% of all adverse event reports for FLUTICASONE.
1,060
Reports of Product dose omission issue with FLUTICASONE
3.3%
of all FLUTICASONE reports
40
Deaths
95
Hospitalizations
How Dangerous Is Product dose omission issue From FLUTICASONE?
Of the 1,060 reports, 40 (3.8%) resulted in death, 95 (9.0%) required hospitalization, and 16 (1.5%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 1,060 reports have been filed with the FAERS database.
What Other Side Effects Does FLUTICASONE Cause?
Drug ineffective (5,872)
Asthma (3,078)
Dyspnoea (3,034)
Off label use (2,488)
Cough (1,824)
Headache (1,812)
Wheezing (1,773)
Epistaxis (1,745)
Product use in unapproved indication (1,717)
Wrong technique in product usage process (1,595)
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 FLUTICASONE Alternatives Have Lower Product dose omission issue Risk?
FLUTICASONE vs FLUTICASONE FUROATE
FLUTICASONE vs FLUTICASONE FUROATE\SALMETEROL
FLUTICASONE vs FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE
FLUTICASONE vs FLUTICASONE FUROATE\VILANTEROL TRIFENATATE
FLUTICASONE vs FLUTICASONE\FLUTICASONE