Does ZILEUTON Cause Product dose omission issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product dose omission issue have been filed in association with ZILEUTON (Zileuton). This represents 11.9% of all adverse event reports for ZILEUTON.
14
Reports of Product dose omission issue with ZILEUTON
11.9%
of all ZILEUTON reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission issue From ZILEUTON?
Of the 14 reports, 3 (21.4%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZILEUTON. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does ZILEUTON Cause?
Off label use (26)
Drug ineffective (18)
Drug ineffective for unapproved indication (13)
Asthma (10)
Dizziness (7)
Dyspnoea (7)
Headache (7)
Nausea (7)
Hypersensitivity (6)
Cough (5)
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 ZILEUTON Alternatives Have Lower Product dose omission issue Risk?
ZILEUTON vs ZILUCOPLAN
ZILEUTON vs ZIMBERELIMAB
ZILEUTON vs ZINC
ZILEUTON vs ZINC\ZINC
ZILEUTON vs ZIPRASIDONE