Does SIPONIMOD Cause Maternal exposure timing unspecified? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Maternal exposure timing unspecified have been filed in association with SIPONIMOD (MAYZENT). This represents 0.1% of all adverse event reports for SIPONIMOD.
8
Reports of Maternal exposure timing unspecified with SIPONIMOD
0.1%
of all SIPONIMOD reports
0
Deaths
1
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From SIPONIMOD?
Of the 8 reports, 1 (12.5%) required hospitalization.
Is Maternal exposure timing unspecified 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which SIPONIMOD Alternatives Have Lower Maternal exposure timing unspecified Risk?
SIPONIMOD vs SIPULEUCEL-T
SIPONIMOD vs SIROLIMUS
SIPONIMOD vs SIRUKUMAB
SIPONIMOD vs SITAGLIPTIN
SIPONIMOD vs SKYLA