Does FLUTICASONE Cause Intentional product use issue? 282 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 282 reports of Intentional product use issue have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 0.9% of all adverse event reports for FLUTICASONE.
282
Reports of Intentional product use issue with FLUTICASONE
0.9%
of all FLUTICASONE reports
137
Deaths
80
Hospitalizations
How Dangerous Is Intentional product use issue From FLUTICASONE?
Of the 282 reports, 137 (48.6%) resulted in death, 80 (28.4%) required hospitalization, and 57 (20.2%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 282 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which FLUTICASONE Alternatives Have Lower Intentional product use 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