Does FLUTICASONE\SALMETEROL Cause Device mechanical issue? 127 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 127 reports of Device mechanical issue have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.3% of all adverse event reports for FLUTICASONE\SALMETEROL.
127
Reports of Device mechanical issue with FLUTICASONE\SALMETEROL
0.3%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device mechanical issue From FLUTICASONE\SALMETEROL?
Of the 127 reports, 1 (0.8%) required hospitalization.
Is Device mechanical issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 127 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 mechanical issue?
SOMATROPIN (6,411)
INSULIN GLARGINE-YFGN (853)
INSULIN GLARGINE (725)
ALBUTEROL (455)
DEVICE (226)
ETANERCEPT (145)
GLATIRAMER (124)
EXENATIDE (108)
MEDROXYPROGESTERONE (99)
ADALIMUMAB-AFZB (76)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Device mechanical issue Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID