Does FLUTICASONE Cause Wrong technique in product usage process? 1,595 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,595 reports of Wrong technique in product usage process have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 5.0% of all adverse event reports for FLUTICASONE.
1,595
Reports of Wrong technique in product usage process with FLUTICASONE
5.0%
of all FLUTICASONE reports
0
Deaths
31
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FLUTICASONE?
Of the 1,595 reports, 31 (1.9%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 1,595 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)
Therapeutic product effect incomplete (1,508)
What Other Drugs Cause Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which FLUTICASONE Alternatives Have Lower Wrong technique in product usage process 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