Does FLUTICASONE\SALMETEROL Cause Incorrect product storage? 69 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Incorrect product storage have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.1% of all adverse event reports for FLUTICASONE\SALMETEROL.
69
Reports of Incorrect product storage with FLUTICASONE\SALMETEROL
0.1%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
8
Hospitalizations
How Dangerous Is Incorrect product storage From FLUTICASONE\SALMETEROL?
Of the 69 reports, 8 (11.6%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 69 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Incorrect product storage Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID