Does SIPONIMOD Cause Product dose omission issue? 381 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 381 reports of Product dose omission issue have been filed in association with SIPONIMOD (MAYZENT). This represents 4.4% of all adverse event reports for SIPONIMOD.
381
Reports of Product dose omission issue with SIPONIMOD
4.4%
of all SIPONIMOD reports
0
Deaths
86
Hospitalizations
How Dangerous Is Product dose omission issue From SIPONIMOD?
Of the 381 reports, 86 (22.6%) required hospitalization, and 4 (1.0%) 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 SIPONIMOD. However, 381 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 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 SIPONIMOD Alternatives Have Lower Product dose omission issue Risk?
SIPONIMOD vs SIPULEUCEL-T
SIPONIMOD vs SIROLIMUS
SIPONIMOD vs SIRUKUMAB
SIPONIMOD vs SITAGLIPTIN
SIPONIMOD vs SKYLA