Does OZANIMOD Cause Product dose omission in error? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Product dose omission in error have been filed in association with OZANIMOD (ZEPOSIA 7-Day Starter Pack). This represents 0.3% of all adverse event reports for OZANIMOD.
27
Reports of Product dose omission in error with OZANIMOD
0.3%
of all OZANIMOD reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From OZANIMOD?
Of the 27 reports, 1 (3.7%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OZANIMOD. However, 27 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)
Product dose omission issue (325)
Nausea (267)
Diarrhoea (253)
Colitis ulcerative (246)
Pain (228)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which OZANIMOD Alternatives Have Lower Product dose omission in error Risk?
OZANIMOD vs PACLITAXEL
OZANIMOD vs PACRITINIB
OZANIMOD vs PALBOCICLIB
OZANIMOD vs PALIPERIDONE
OZANIMOD vs PALIVIZUMAB