Does FLUTICASONE\SALMETEROL Cause Device use issue? 126 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 126 reports of Device use issue have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.3% of all adverse event reports for FLUTICASONE\SALMETEROL.
126
Reports of Device use issue with FLUTICASONE\SALMETEROL
0.3%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Device use issue From FLUTICASONE\SALMETEROL?
Of the 126 reports, 5 (4.0%) required hospitalization.
Is Device use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 126 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 issue?
SOMATROPIN (2,571)
LEVONORGESTREL (2,489)
COPPER (1,318)
BUDESONIDE\FORMOTEROL (1,236)
EXENATIDE (992)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (976)
DUPILUMAB (528)
ALIROCUMAB (471)
INSULIN GLARGINE (469)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (459)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Device use issue Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID