Does FLUTICASONE\SALMETEROL Cause Device malfunction? 189 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 189 reports of Device malfunction have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.4% of all adverse event reports for FLUTICASONE\SALMETEROL.
189
Reports of Device malfunction with FLUTICASONE\SALMETEROL
0.4%
of all FLUTICASONE\SALMETEROL reports
1
Deaths
9
Hospitalizations
How Dangerous Is Device malfunction From FLUTICASONE\SALMETEROL?
Of the 189 reports, 1 (0.5%) resulted in death, 9 (4.8%) required hospitalization, and 4 (2.1%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 189 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 malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Device malfunction Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID