Does SIPONIMOD Cause Product prescribing error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product prescribing error have been filed in association with SIPONIMOD (MAYZENT). This represents 0.1% of all adverse event reports for SIPONIMOD.
8
Reports of Product prescribing error with SIPONIMOD
0.1%
of all SIPONIMOD reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product prescribing error From SIPONIMOD?
Of the 8 reports.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIPONIMOD. However, 8 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 prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which SIPONIMOD Alternatives Have Lower Product prescribing error Risk?
SIPONIMOD vs SIPULEUCEL-T
SIPONIMOD vs SIROLIMUS
SIPONIMOD vs SIRUKUMAB
SIPONIMOD vs SITAGLIPTIN
SIPONIMOD vs SKYLA