Does FLUTICASONE\SALMETEROL Cause Product dose omission issue? 2,118 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,118 reports of Product dose omission issue have been filed in association with FLUTICASONE\SALMETEROL. This represents 4.4% of all adverse event reports for FLUTICASONE\SALMETEROL.
2,118
Reports of Product dose omission issue with FLUTICASONE\SALMETEROL
4.4%
of all FLUTICASONE\SALMETEROL reports
32
Deaths
147
Hospitalizations
How Dangerous Is Product dose omission issue From FLUTICASONE\SALMETEROL?
Of the 2,118 reports, 32 (1.5%) resulted in death, 147 (6.9%) required hospitalization, and 12 (0.6%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUTICASONE\SALMETEROL. However, 2,118 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which FLUTICASONE\SALMETEROL Alternatives Have Lower Product dose omission issue Risk?
FLUTICASONE\SALMETEROL vs FLUVASTATIN
FLUTICASONE\SALMETEROL vs FLUVOXAMINE
FLUTICASONE\SALMETEROL vs FOLATE
FLUTICASONE\SALMETEROL vs FOLIC ACID
FLUTICASONE\SALMETEROL vs FOLINIC ACID