Does FLUTICASONE\SALMETEROL Cause Product dispensing error? 208 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 208 reports of Product dispensing error have been filed in association with FLUTICASONE\SALMETEROL. This represents 0.4% of all adverse event reports for FLUTICASONE\SALMETEROL.
208
Reports of Product dispensing error with FLUTICASONE\SALMETEROL
0.4%
of all FLUTICASONE\SALMETEROL reports
0
Deaths
23
Hospitalizations
How Dangerous Is Product dispensing error From FLUTICASONE\SALMETEROL?
Of the 208 reports, 23 (11.1%) required hospitalization.
Is Product dispensing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 208 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 dispensing error?
INSULIN GLARGINE (1,048)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (692)
ADALIMUMAB (386)
SEMAGLUTIDE (379)
PREGABALIN (323)
NIRMATRELVIR\RITONAVIR (310)
ETANERCEPT (305)
SECUKINUMAB (300)
APIXABAN (299)
PALBOCICLIB (299)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Product dispensing error Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID