Does BRENTUXIMAB VEDOTIN Cause Febrile neutropenia? 684 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 684 reports of Febrile neutropenia have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 7.0% of all adverse event reports for BRENTUXIMAB VEDOTIN.
684
Reports of Febrile neutropenia with BRENTUXIMAB VEDOTIN
7.0%
of all BRENTUXIMAB VEDOTIN reports
80
Deaths
477
Hospitalizations
How Dangerous Is Febrile neutropenia From BRENTUXIMAB VEDOTIN?
Of the 684 reports, 80 (11.7%) resulted in death, 477 (69.7%) required hospitalization, and 109 (15.9%) 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 BRENTUXIMAB VEDOTIN.
What Other Side Effects Does BRENTUXIMAB VEDOTIN Cause?
Off label use (1,370)
Neuropathy peripheral (695)
Pyrexia (693)
Death (602)
Neutropenia (561)
Hodgkin's disease (512)
Nausea (392)
Diarrhoea (385)
Anaemia (374)
Thrombocytopenia (358)
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 BRENTUXIMAB VEDOTIN Alternatives Have Lower Febrile neutropenia Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB