Does SIPONIMOD Cause Wrong product administered? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Wrong product administered have been filed in association with SIPONIMOD (MAYZENT). This represents 0.1% of all adverse event reports for SIPONIMOD.
6
Reports of Wrong product administered with SIPONIMOD
0.1%
of all SIPONIMOD reports
1
Deaths
1
Hospitalizations
How Dangerous Is Wrong product administered From SIPONIMOD?
Of the 6 reports, 1 (16.7%) resulted in death, 1 (16.7%) required hospitalization.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIPONIMOD. However, 6 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which SIPONIMOD Alternatives Have Lower Wrong product administered Risk?
SIPONIMOD vs SIPULEUCEL-T
SIPONIMOD vs SIROLIMUS
SIPONIMOD vs SIRUKUMAB
SIPONIMOD vs SITAGLIPTIN
SIPONIMOD vs SKYLA