Does FLUTICASONE\SALMETEROL Cause Device delivery system issue? 162 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 162 reports of Device delivery system issue have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.3% of all adverse event reports for FLUTICASONE\SALMETEROL.
162
Reports of Device delivery system issue with FLUTICASONE\SALMETEROL
0.3%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device delivery system issue From FLUTICASONE\SALMETEROL?
Of the 162 reports.
Is Device delivery system issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 162 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 delivery system issue?
ALBUTEROL (9,509)
SOMATROPIN (1,848)
EXENATIDE (1,533)
BUDESONIDE\FORMOTEROL (1,260)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (1,181)
BUDESONIDE\FORMOTEROL\GLYCOPYRRONIUM (523)
LEVALBUTEROL (459)
MOMETASONE FUROATE\OLOPATADINE (347)
ABATACEPT (342)
PEGFILGRASTIM (323)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Device delivery system issue Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID