Does FLUTICASONE\SALMETEROL Cause Device use error? 1,749 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,749 reports of Device use error have been filed in association with FLUTICASONE\SALMETEROL. This represents 3.7% of all adverse event reports for FLUTICASONE\SALMETEROL.
1,749
Reports of Device use error with FLUTICASONE\SALMETEROL
3.7%
of all FLUTICASONE\SALMETEROL reports
1
Deaths
96
Hospitalizations
How Dangerous Is Device use error From FLUTICASONE\SALMETEROL?
Of the 1,749 reports, 1 (0.1%) resulted in death, 96 (5.5%) required hospitalization, and 1 (0.1%) were considered life-threatening.
Is Device use error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 1,749 reports have been filed with the FAERS database.
What Other Side Effects Does FLUTICASONE\SALMETEROL Cause?
Dyspnoea (9,783)
Asthma (7,985)
Drug ineffective (7,037)
Cough (4,111)
Wheezing (3,948)
Pneumonia (3,217)
Product quality issue (2,986)
Malaise (2,588)
Therapeutic product effect incomplete (2,402)
Wrong technique in device usage process (2,259)
What Other Drugs Cause Device use error?
PEGFILGRASTIM (6,001)
ALBUTEROL (5,215)
ALBIGLUTIDE (4,056)
EVOLOCUMAB (4,002)
SOMATROPIN (2,801)
FLUTICASONE (783)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (766)
ERENUMAB-AOOE (711)
ETANERCEPT (665)
TREPROSTINIL (563)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Device use error Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID