Does FLUTICASONE\SALMETEROL Cause Device issue? 575 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 575 reports of Device issue have been filed in association with FLUTICASONE\SALMETEROL. This represents 1.2% of all adverse event reports for FLUTICASONE\SALMETEROL.
575
Reports of Device issue with FLUTICASONE\SALMETEROL
1.2%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
13
Hospitalizations
How Dangerous Is Device issue From FLUTICASONE\SALMETEROL?
Of the 575 reports, 13 (2.3%) required hospitalization, and 2 (0.3%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 575 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Device issue Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID