Does BRENTUXIMAB VEDOTIN Cause Hypersensitivity? 95 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 95 reports of Hypersensitivity have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 1.0% of all adverse event reports for BRENTUXIMAB VEDOTIN.
95
Reports of Hypersensitivity with BRENTUXIMAB VEDOTIN
1.0%
of all BRENTUXIMAB VEDOTIN reports
14
Deaths
45
Hospitalizations
How Dangerous Is Hypersensitivity From BRENTUXIMAB VEDOTIN?
Of the 95 reports, 14 (14.7%) resulted in death, 45 (47.4%) required hospitalization, and 14 (14.7%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
Yes, Hypersensitivity 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 Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which BRENTUXIMAB VEDOTIN Alternatives Have Lower Hypersensitivity Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB