Does FLUTICASONE\SALMETEROL Cause Product storage error? 307 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 307 reports of Product storage error have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.6% of all adverse event reports for FLUTICASONE\SALMETEROL.
307
Reports of Product storage error with FLUTICASONE\SALMETEROL
0.6%
of all FLUTICASONE\SALMETEROL reports
1
Deaths
10
Hospitalizations
How Dangerous Is Product storage error From FLUTICASONE\SALMETEROL?
Of the 307 reports, 1 (0.3%) resulted in death, 10 (3.3%) required hospitalization.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 307 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 Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Product storage error Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID