Does FLUTICASONE Cause Condition aggravated? 1,187 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,187 reports of Condition aggravated have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 3.7% of all adverse event reports for FLUTICASONE.
1,187
Reports of Condition aggravated with FLUTICASONE
3.7%
of all FLUTICASONE reports
239
Deaths
430
Hospitalizations
How Dangerous Is Condition aggravated From FLUTICASONE?
Of the 1,187 reports, 239 (20.1%) resulted in death, 430 (36.2%) required hospitalization, and 197 (16.6%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 1,187 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which FLUTICASONE Alternatives Have Lower Condition aggravated 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