Does SIPONIMOD Cause Product use issue? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Product use issue have been filed in association with SIPONIMOD (MAYZENT). This represents 0.5% of all adverse event reports for SIPONIMOD.
41
Reports of Product use issue with SIPONIMOD
0.5%
of all SIPONIMOD reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product use issue From SIPONIMOD?
Of the 41 reports, 6 (14.6%) required hospitalization, and 1 (2.4%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIPONIMOD. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does SIPONIMOD Cause?
Fatigue (958)
Headache (862)
Dizziness (654)
Gait disturbance (506)
Multiple sclerosis relapse (504)
Fall (478)
Multiple sclerosis (455)
Lymphocyte count decreased (398)
Nausea (397)
Drug ineffective (396)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which SIPONIMOD Alternatives Have Lower Product use issue Risk?
SIPONIMOD vs SIPULEUCEL-T
SIPONIMOD vs SIROLIMUS
SIPONIMOD vs SIRUKUMAB
SIPONIMOD vs SITAGLIPTIN
SIPONIMOD vs SKYLA