Does OZANIMOD Cause Product prescribing issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product prescribing issue have been filed in association with OZANIMOD (ZEPOSIA 7-Day Starter Pack). This represents 0.1% of all adverse event reports for OZANIMOD.
9
Reports of Product prescribing issue with OZANIMOD
0.1%
of all OZANIMOD reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing issue From OZANIMOD?
Of the 9 reports.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OZANIMOD. However, 9 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which OZANIMOD Alternatives Have Lower Product prescribing issue Risk?
OZANIMOD vs PACLITAXEL
OZANIMOD vs PACRITINIB
OZANIMOD vs PALBOCICLIB
OZANIMOD vs PALIPERIDONE
OZANIMOD vs PALIVIZUMAB