Does GLOFITAMAB Cause Multiple organ dysfunction syndrome? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Multiple organ dysfunction syndrome have been filed in association with GLOFITAMAB (Columvi). This represents 0.7% of all adverse event reports for GLOFITAMAB.
8
Reports of Multiple organ dysfunction syndrome with GLOFITAMAB
0.7%
of all GLOFITAMAB reports
6
Deaths
3
Hospitalizations
How Dangerous Is Multiple organ dysfunction syndrome From GLOFITAMAB?
Of the 8 reports, 6 (75.0%) resulted in death, 3 (37.5%) required hospitalization, and 2 (25.0%) were considered life-threatening.
Is Multiple organ dysfunction syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GLOFITAMAB. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does GLOFITAMAB Cause?
Cytokine release syndrome (415)
Disease progression (183)
Off label use (129)
Death (125)
Neutropenia (109)
Pyrexia (78)
Febrile neutropenia (69)
Covid-19 (62)
Drug ineffective (53)
Immune effector cell-associated neurotoxicity syndrome (45)
What Other Drugs Cause Multiple organ dysfunction syndrome?
TACROLIMUS (1,847)
CYCLOPHOSPHAMIDE (1,597)
MYCOPHENOLATE MOFETIL (1,566)
PREDNISONE (1,525)
DEXAMETHASONE (1,355)
METHOTREXATE (1,317)
METHYLPREDNISOLONE (1,278)
RITUXIMAB (1,188)
PREDNISOLONE (1,154)
CYCLOSPORINE (933)
Which GLOFITAMAB Alternatives Have Lower Multiple organ dysfunction syndrome Risk?
GLOFITAMAB vs GLOFITAMAB-GXBM
GLOFITAMAB vs GLUCAGON
GLOFITAMAB vs GLUCAGON\GLUCAGON\WATER
GLOFITAMAB vs GLUCARPIDASE
GLOFITAMAB vs GLUCOPHAGE