Does FLUTICASONE Cause Recalled product administered? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Recalled product administered have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 0.2% of all adverse event reports for FLUTICASONE.
71
Reports of Recalled product administered with FLUTICASONE
0.2%
of all FLUTICASONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Recalled product administered From FLUTICASONE?
Of the 71 reports, 1 (1.4%) required hospitalization, and 1 (1.4%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 71 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 Recalled product administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which FLUTICASONE Alternatives Have Lower Recalled 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