Does SALMETEROL Cause Product dose omission issue? 57 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 57 reports of Product dose omission issue have been filed in association with SALMETEROL (SEREVENT DISKUS). This represents 3.2% of all adverse event reports for SALMETEROL.
57
Reports of Product dose omission issue with SALMETEROL
3.2%
of all SALMETEROL reports
7
Deaths
25
Hospitalizations
How Dangerous Is Product dose omission issue From SALMETEROL?
Of the 57 reports, 7 (12.3%) resulted in death, 25 (43.9%) required hospitalization, and 6 (10.5%) 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 SALMETEROL. However, 57 reports have been filed with the FAERS database.
What Other Side Effects Does SALMETEROL Cause?
Dyspnoea (345)
Drug ineffective (315)
Asthma (274)
Cough (219)
Chest discomfort (188)
Wheezing (186)
Off label use (152)
Dysphonia (133)
Obstructive airways disorder (126)
Drug hypersensitivity (118)
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 SALMETEROL Alternatives Have Lower Product dose omission issue Risk?
SALMETEROL vs SAMSCA
SALMETEROL vs SANDOSTATIN LAR
SALMETEROL vs SANDOZ FENTANYL SYSTEM
SALMETEROL vs SAPROPTERIN
SALMETEROL vs SAQUINAVIR