Does FLUTICASONE Cause Incorrect product administration duration? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Incorrect product administration duration have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 0.3% of all adverse event reports for FLUTICASONE.
84
Reports of Incorrect product administration duration with FLUTICASONE
0.3%
of all FLUTICASONE reports
4
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product administration duration From FLUTICASONE?
Of the 84 reports, 4 (4.8%) resulted in death, 4 (4.8%) required hospitalization, and 6 (7.1%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 84 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which FLUTICASONE Alternatives Have Lower Incorrect product administration duration 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