Does FLUTICASONE\SALMETEROL Cause Product prescribing error? 129 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 129 reports of Product prescribing error have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.3% of all adverse event reports for FLUTICASONE\SALMETEROL.
129
Reports of Product prescribing error with FLUTICASONE\SALMETEROL
0.3%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
46
Hospitalizations
How Dangerous Is Product prescribing error From FLUTICASONE\SALMETEROL?
Of the 129 reports, 46 (35.7%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 129 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Product prescribing error Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID