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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FLUTICASONE Cause Device defective? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Device defective have been filed in association with FLUTICASONE (ADVAIR DISKUS). This represents 0.1% of all adverse event reports for FLUTICASONE.

40
Reports of Device defective with FLUTICASONE
0.1%
of all FLUTICASONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device defective From FLUTICASONE?

Of the 40 reports.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FLUTICASONE. However, 40 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which FLUTICASONE Alternatives Have Lower Device defective 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

Related Pages

FLUTICASONE Full Profile All Device defective Reports All Drugs Causing Device defective FLUTICASONE Demographics