Does FLUTICASONE Cause Product quality issue? 877 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 877 reports of Product quality issue have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 2.7% of all adverse event reports for FLUTICASONE.
877
Reports of Product quality issue with FLUTICASONE
2.7%
of all FLUTICASONE reports
118
Deaths
83
Hospitalizations
How Dangerous Is Product quality issue From FLUTICASONE?
Of the 877 reports, 118 (13.5%) resulted in death, 83 (9.5%) required hospitalization, and 57 (6.5%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 877 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which FLUTICASONE Alternatives Have Lower Product quality 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