Does OZANIMOD Cause Product dose omission issue? 325 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 325 reports of Product dose omission issue have been filed in association with OZANIMOD (ZEPOSIA 7-Day Starter Pack). This represents 4.1% of all adverse event reports for OZANIMOD.
325
Reports of Product dose omission issue with OZANIMOD
4.1%
of all OZANIMOD reports
0
Deaths
17
Hospitalizations
How Dangerous Is Product dose omission issue From OZANIMOD?
Of the 325 reports, 17 (5.2%) required hospitalization, and 1 (0.3%) 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 OZANIMOD. However, 325 reports have been filed with the FAERS database.
What Other Side Effects Does OZANIMOD Cause?
Fatigue (707)
Multiple sclerosis relapse (567)
Drug ineffective (517)
Headache (490)
Dizziness (329)
Nausea (267)
Diarrhoea (253)
Colitis ulcerative (246)
Pain (228)
Back pain (206)
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 OZANIMOD Alternatives Have Lower Product dose omission issue Risk?
OZANIMOD vs PACLITAXEL
OZANIMOD vs PACRITINIB
OZANIMOD vs PALBOCICLIB
OZANIMOD vs PALIPERIDONE
OZANIMOD vs PALIVIZUMAB