Does BRENTUXIMAB VEDOTIN Cause Sepsis? 249 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 249 reports of Sepsis have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 2.6% of all adverse event reports for BRENTUXIMAB VEDOTIN.
249
Reports of Sepsis with BRENTUXIMAB VEDOTIN
2.6%
of all BRENTUXIMAB VEDOTIN reports
128
Deaths
165
Hospitalizations
How Dangerous Is Sepsis From BRENTUXIMAB VEDOTIN?
Of the 249 reports, 128 (51.4%) resulted in death, 165 (66.3%) required hospitalization, and 28 (11.2%) were considered life-threatening.
Is Sepsis Listed in the Official Label?
Yes, Sepsis 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)
Febrile neutropenia (684)
Death (602)
Neutropenia (561)
Hodgkin's disease (512)
Nausea (392)
Diarrhoea (385)
Anaemia (374)
What Other Drugs Cause Sepsis?
RITUXIMAB (4,043)
CYCLOPHOSPHAMIDE (4,041)
METHOTREXATE (3,933)
ADALIMUMAB (3,169)
DEXAMETHASONE (3,150)
LENALIDOMIDE (2,956)
VINCRISTINE (2,791)
DOXORUBICIN (2,740)
PREDNISONE (2,634)
PREDNISOLONE (2,281)
Which BRENTUXIMAB VEDOTIN Alternatives Have Lower Sepsis Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB