Does FLUTICASONE\SALMETEROL Cause Complication associated with device? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Complication associated with device have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.0% of all adverse event reports for FLUTICASONE\SALMETEROL.
8
Reports of Complication associated with device with FLUTICASONE\SALMETEROL
0.0%
of all FLUTICASONE\SALMETEROL reports
2
Deaths
4
Hospitalizations
How Dangerous Is Complication associated with device From FLUTICASONE\SALMETEROL?
Of the 8 reports, 2 (25.0%) resulted in death, 4 (50.0%) required hospitalization.
Is Complication associated with device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 8 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 Complication associated with device?
ETONOGESTREL (6,047)
COPPER (1,083)
BACLOFEN (525)
TREPROSTINIL (422)
EPOPROSTENOL (399)
LEVONORGESTREL (344)
ADALIMUMAB (269)
CARBIDOPA\LEVODOPA (169)
MACITENTAN (169)
TEDUGLUTIDE (133)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Complication associated with device Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID