Does FLUTICASONE Cause Product use in unapproved indication? 1,717 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,717 reports of Product use in unapproved indication have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 5.4% of all adverse event reports for FLUTICASONE.
1,717
Reports of Product use in unapproved indication with FLUTICASONE
5.4%
of all FLUTICASONE reports
222
Deaths
290
Hospitalizations
How Dangerous Is Product use in unapproved indication From FLUTICASONE?
Of the 1,717 reports, 222 (12.9%) resulted in death, 290 (16.9%) required hospitalization, and 135 (7.9%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 1,717 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)
Wrong technique in product usage process (1,595)
Therapeutic product effect incomplete (1,508)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which FLUTICASONE Alternatives Have Lower Product use in unapproved indication 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