Does FLUTICASONE Cause Device use error? 783 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 783 reports of Device use error have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 2.5% of all adverse event reports for FLUTICASONE.
783
Reports of Device use error with FLUTICASONE
2.5%
of all FLUTICASONE reports
0
Deaths
15
Hospitalizations
How Dangerous Is Device use error From FLUTICASONE?
Of the 783 reports, 15 (1.9%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 783 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 Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE\SALMETEROL (1,749)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which FLUTICASONE Alternatives Have Lower Device use error 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