Does BRENTUXIMAB VEDOTIN Cause Hepatic function abnormal? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Hepatic function abnormal have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 0.6% of all adverse event reports for BRENTUXIMAB VEDOTIN.
55
Reports of Hepatic function abnormal with BRENTUXIMAB VEDOTIN
0.6%
of all BRENTUXIMAB VEDOTIN reports
16
Deaths
19
Hospitalizations
How Dangerous Is Hepatic function abnormal From BRENTUXIMAB VEDOTIN?
Of the 55 reports, 16 (29.1%) resulted in death, 19 (34.5%) required hospitalization, and 4 (7.3%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRENTUXIMAB VEDOTIN. However, 55 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which BRENTUXIMAB VEDOTIN Alternatives Have Lower Hepatic function abnormal Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB