Does BEVACIZUMAB-BVZR Cause Condition aggravated? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Condition aggravated have been filed in association with BEVACIZUMAB-BVZR. This represents 2.1% of all adverse event reports for BEVACIZUMAB-BVZR.
12
Reports of Condition aggravated with BEVACIZUMAB-BVZR
2.1%
of all BEVACIZUMAB-BVZR reports
3
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From BEVACIZUMAB-BVZR?
Of the 12 reports, 3 (25.0%) resulted in death, 7 (58.3%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB-BVZR. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does BEVACIZUMAB-BVZR Cause?
Off label use (159)
Death (149)
Neoplasm progression (80)
Fatigue (57)
Hypertension (41)
Blood pressure increased (39)
Weight decreased (39)
Weight increased (34)
Inappropriate schedule of product administration (28)
Malaise (28)
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-BVZR Alternatives Have Lower Condition aggravated Risk?
BEVACIZUMAB-BVZR vs BEVACIZUMAB-MALY
BEVACIZUMAB-BVZR vs BEXAROTENE
BEVACIZUMAB-BVZR vs BEZAFIBRATE
BEVACIZUMAB-BVZR vs BEZLOTOXUMAB
BEVACIZUMAB-BVZR vs BGB-11417