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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does GLOFITAMAB Cause Febrile neutropenia? 69 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 69 reports of Febrile neutropenia have been filed in association with GLOFITAMAB (Columvi). This represents 6.2% of all adverse event reports for GLOFITAMAB.

69
Reports of Febrile neutropenia with GLOFITAMAB
6.2%
of all GLOFITAMAB reports
2
Deaths
55
Hospitalizations

How Dangerous Is Febrile neutropenia From GLOFITAMAB?

Of the 69 reports, 2 (2.9%) resulted in death, 55 (79.7%) required hospitalization, and 7 (10.1%) were considered life-threatening.

Is Febrile neutropenia Listed in the Official Label?

Yes, Febrile neutropenia is listed as a known adverse reaction in the official FDA drug label for GLOFITAMAB.

What Other Side Effects Does GLOFITAMAB Cause?

Cytokine release syndrome (415) Disease progression (183) Off label use (129) Death (125) Neutropenia (109) Pyrexia (78) Covid-19 (62) Drug ineffective (53) Immune effector cell-associated neurotoxicity syndrome (45) Infection (44)

What Other Drugs Cause Febrile neutropenia?

CYCLOPHOSPHAMIDE (11,318) DOXORUBICIN (8,844) VINCRISTINE (8,676) RITUXIMAB (6,382) CYTARABINE (6,142) METHOTREXATE (6,091) ETOPOSIDE (5,966) CARBOPLATIN (4,888) DEXAMETHASONE (4,382) PREDNISONE (3,956)

Which GLOFITAMAB Alternatives Have Lower Febrile neutropenia Risk?

GLOFITAMAB vs GLOFITAMAB-GXBM GLOFITAMAB vs GLUCAGON GLOFITAMAB vs GLUCAGON\GLUCAGON\WATER GLOFITAMAB vs GLUCARPIDASE GLOFITAMAB vs GLUCOPHAGE

Related Pages

GLOFITAMAB Full Profile All Febrile neutropenia Reports All Drugs Causing Febrile neutropenia GLOFITAMAB Demographics