Does FLUTICASONE Cause Expired product administered? 304 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 304 reports of Expired product administered have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 1.0% of all adverse event reports for FLUTICASONE.
304
Reports of Expired product administered with FLUTICASONE
1.0%
of all FLUTICASONE reports
0
Deaths
19
Hospitalizations
How Dangerous Is Expired product administered From FLUTICASONE?
Of the 304 reports, 19 (6.3%) required hospitalization.
Is Expired product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 304 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 Expired product administered?
POLYETHYLENE GLYCOL 3350 (1,637)
NAPROXEN (1,305)
ALBUTEROL (1,233)
LORATADINE (1,095)
MINOXIDIL (982)
ACETAMINOPHEN (797)
INSULIN LISPRO (770)
FLUTICASONE\SALMETEROL (753)
CETIRIZINE (714)
DICLOFENAC (714)
Which FLUTICASONE Alternatives Have Lower Expired product administered 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