Does FORMOTEROL Cause Product dose omission issue? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Product dose omission issue have been filed in association with FORMOTEROL (Formoterol fumarate). This represents 2.5% of all adverse event reports for FORMOTEROL.
70
Reports of Product dose omission issue with FORMOTEROL
2.5%
of all FORMOTEROL reports
0
Deaths
59
Hospitalizations
How Dangerous Is Product dose omission issue From FORMOTEROL?
Of the 70 reports, 59 (84.3%) required hospitalization, and 10 (14.3%) 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 FORMOTEROL. However, 70 reports have been filed with the FAERS database.
What Other Side Effects Does FORMOTEROL Cause?
Asthma (1,204)
Dyspnoea (1,090)
Wheezing (632)
Cough (553)
Obstructive airways disorder (504)
Therapeutic product effect incomplete (467)
Drug ineffective (456)
Gastrooesophageal reflux disease (434)
Full blood count abnormal (344)
Loss of personal independence in daily activities (307)
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 FORMOTEROL Alternatives Have Lower Product dose omission issue Risk?
FORMOTEROL vs FORMOTEROL\GLYCOPYRROLATE
FORMOTEROL vs FORMOTEROL\MOMETASONE
FORMOTEROL vs FORMOTEROL\MOMETASONE FUROATE
FORMOTEROL vs FORTEO
FORMOTEROL vs FOSAMAX