Does BEVACIZUMAB Cause Condition aggravated? 558 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 558 reports of Condition aggravated have been filed in association with BEVACIZUMAB (JOBEVNE). This represents 0.7% of all adverse event reports for BEVACIZUMAB.
558
Reports of Condition aggravated with BEVACIZUMAB
0.7%
of all BEVACIZUMAB reports
96
Deaths
241
Hospitalizations
How Dangerous Is Condition aggravated From BEVACIZUMAB?
Of the 558 reports, 96 (17.2%) resulted in death, 241 (43.2%) required hospitalization, and 26 (4.7%) 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 BEVACIZUMAB. However, 558 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 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 BEVACIZUMAB Alternatives Have Lower Condition aggravated Risk?
BEVACIZUMAB vs BEVACIZUMAB-AWWB
BEVACIZUMAB vs BEVACIZUMAB-BVZR
BEVACIZUMAB vs BEVACIZUMAB-MALY
BEVACIZUMAB vs BEXAROTENE
BEVACIZUMAB vs BEYAZ