Does BRENTUXIMAB VEDOTIN Cause Condition aggravated? 142 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 142 reports of Condition aggravated have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 1.5% of all adverse event reports for BRENTUXIMAB VEDOTIN.
142
Reports of Condition aggravated with BRENTUXIMAB VEDOTIN
1.5%
of all BRENTUXIMAB VEDOTIN reports
52
Deaths
56
Hospitalizations
How Dangerous Is Condition aggravated From BRENTUXIMAB VEDOTIN?
Of the 142 reports, 52 (36.6%) resulted in death, 56 (39.4%) required hospitalization, and 24 (16.9%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRENTUXIMAB VEDOTIN. However, 142 reports have been filed with the FAERS database.
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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which BRENTUXIMAB VEDOTIN Alternatives Have Lower Condition aggravated Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB