Does BEVACIZUMAB Cause Hypertransaminasaemia? 94 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 94 reports of Hypertransaminasaemia have been filed in association with BEVACIZUMAB (JOBEVNE). This represents 0.1% of all adverse event reports for BEVACIZUMAB.
94
Reports of Hypertransaminasaemia with BEVACIZUMAB
0.1%
of all BEVACIZUMAB reports
11
Deaths
18
Hospitalizations
How Dangerous Is Hypertransaminasaemia From BEVACIZUMAB?
Of the 94 reports, 11 (11.7%) resulted in death, 18 (19.1%) required hospitalization, and 6 (6.4%) were considered life-threatening.
Is Hypertransaminasaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB. However, 94 reports have been filed with the FAERS database.
What Other Side Effects Does BEVACIZUMAB Cause?
Off label use (12,094)
Death (8,493)
Diarrhoea (4,911)
Disease progression (4,653)
Fatigue (4,572)
Nausea (4,357)
Hypertension (4,309)
Anaemia (3,221)
Vomiting (3,193)
Neutropenia (2,875)
What Other Drugs Cause Hypertransaminasaemia?
METHOTREXATE (436)
ACETAMINOPHEN (326)
PACLITAXEL (318)
CARBOPLATIN (304)
PEMBROLIZUMAB (231)
ATORVASTATIN (207)
CYCLOPHOSPHAMIDE (202)
PREDNISONE (198)
GEMCITABINE (196)
DEXAMETHASONE (169)
Which BEVACIZUMAB Alternatives Have Lower Hypertransaminasaemia Risk?
BEVACIZUMAB vs BEVACIZUMAB-AWWB
BEVACIZUMAB vs BEVACIZUMAB-BVZR
BEVACIZUMAB vs BEVACIZUMAB-MALY
BEVACIZUMAB vs BEXAROTENE
BEVACIZUMAB vs BEYAZ