Does FLUTICASONE FUROATE Cause Device use error? 99 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 99 reports of Device use error have been filed in association with FLUTICASONE FUROATE (Fluticasone Furoate Ellipta). This represents 1.3% of all adverse event reports for FLUTICASONE FUROATE.
99
Reports of Device use error with FLUTICASONE FUROATE
1.3%
of all FLUTICASONE FUROATE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Device use error From FLUTICASONE FUROATE?
Of the 99 reports, 2 (2.0%) required hospitalization, and 1 (1.0%) 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 FUROATE. However, 99 reports have been filed with the FAERS database.
What Other Side Effects Does FLUTICASONE FUROATE Cause?
Drug ineffective (1,905)
Dyspnoea (1,161)
Asthma (1,119)
Therapeutic product effect incomplete (834)
Wheezing (791)
Macular degeneration (723)
Off label use (695)
Product use in unapproved indication (627)
Cough (618)
Condition aggravated (482)
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 (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
Which FLUTICASONE FUROATE Alternatives Have Lower Device use error Risk?
FLUTICASONE FUROATE vs FLUTICASONE FUROATE\SALMETEROL
FLUTICASONE FUROATE vs FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE
FLUTICASONE FUROATE vs FLUTICASONE FUROATE\VILANTEROL TRIFENATATE
FLUTICASONE FUROATE vs FLUTICASONE\FLUTICASONE
FLUTICASONE FUROATE vs FLUTICASONE\FORMOTEROL