Does SIPONIMOD Cause Wrong technique in product usage process? 46 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 46 reports of Wrong technique in product usage process have been filed in association with SIPONIMOD (MAYZENT). This represents 0.5% of all adverse event reports for SIPONIMOD.
46
Reports of Wrong technique in product usage process with SIPONIMOD
0.5%
of all SIPONIMOD reports
0
Deaths
10
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SIPONIMOD?
Of the 46 reports, 10 (21.7%) required hospitalization, and 1 (2.2%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SIPONIMOD. However, 46 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 technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SIPONIMOD Alternatives Have Lower Wrong technique in product usage process Risk?
SIPONIMOD vs SIPULEUCEL-T
SIPONIMOD vs SIROLIMUS
SIPONIMOD vs SIRUKUMAB
SIPONIMOD vs SITAGLIPTIN
SIPONIMOD vs SKYLA