Does BEVACIZUMAB-AWWB Cause Adverse event? 143 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 143 reports of Adverse event have been filed in association with BEVACIZUMAB-AWWB. This represents 3.5% of all adverse event reports for BEVACIZUMAB-AWWB.
143
Reports of Adverse event with BEVACIZUMAB-AWWB
3.5%
of all BEVACIZUMAB-AWWB reports
0
Deaths
1
Hospitalizations
How Dangerous Is Adverse event From BEVACIZUMAB-AWWB?
Of the 143 reports, 1 (0.7%) required hospitalization.
Is Adverse event Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB-AWWB. However, 143 reports have been filed with the FAERS database.
What Other Side Effects Does BEVACIZUMAB-AWWB Cause?
Off label use (441)
Product storage error (437)
Circumstance or information capable of leading to medication error (346)
Hypertension (187)
Blood pressure increased (163)
Disease progression (160)
Product dose omission issue (158)
Platelet count decreased (118)
Fatigue (104)
Intercepted product administration error (97)
What Other Drugs Cause Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which BEVACIZUMAB-AWWB Alternatives Have Lower Adverse event Risk?
BEVACIZUMAB-AWWB vs BEVACIZUMAB-BVZR
BEVACIZUMAB-AWWB vs BEVACIZUMAB-MALY
BEVACIZUMAB-AWWB vs BEXAROTENE
BEVACIZUMAB-AWWB vs BEZAFIBRATE
BEVACIZUMAB-AWWB vs BEZLOTOXUMAB