Does BEVACIZUMAB Cause Intentional product use issue? 2,149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 2,149 reports of Intentional product use issue have been filed in association with BEVACIZUMAB (JOBEVNE). This represents 2.8% of all adverse event reports for BEVACIZUMAB.
2,149
Reports of Intentional product use issue with BEVACIZUMAB
2.8%
of all BEVACIZUMAB reports
384
Deaths
399
Hospitalizations
How Dangerous Is Intentional product use issue From BEVACIZUMAB?
Of the 2,149 reports, 384 (17.9%) resulted in death, 399 (18.6%) required hospitalization, and 37 (1.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB. However, 2,149 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which BEVACIZUMAB Alternatives Have Lower Intentional product use issue Risk?
BEVACIZUMAB vs BEVACIZUMAB-AWWB
BEVACIZUMAB vs BEVACIZUMAB-BVZR
BEVACIZUMAB vs BEVACIZUMAB-MALY
BEVACIZUMAB vs BEXAROTENE
BEVACIZUMAB vs BEYAZ