Does BEVACIZUMAB-AWWB Cause Therapy partial responder? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Therapy partial responder have been filed in association with BEVACIZUMAB-AWWB. This represents 0.3% of all adverse event reports for BEVACIZUMAB-AWWB.
12
Reports of Therapy partial responder with BEVACIZUMAB-AWWB
0.3%
of all BEVACIZUMAB-AWWB reports
3
Deaths
1
Hospitalizations
How Dangerous Is Therapy partial responder From BEVACIZUMAB-AWWB?
Of the 12 reports, 3 (25.0%) resulted in death, 1 (8.3%) required hospitalization, and 1 (8.3%) were considered life-threatening.
Is Therapy partial responder Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB-AWWB. However, 12 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)
Adverse event (143)
Platelet count decreased (118)
Fatigue (104)
What Other Drugs Cause Therapy partial responder?
CYCLOPHOSPHAMIDE (1,397)
RITUXIMAB (1,219)
DEXAMETHASONE (1,199)
PREDNISONE (1,176)
PEMBROLIZUMAB (1,125)
CARBOPLATIN (1,096)
DOXORUBICIN (834)
METHOTREXATE (775)
VINCRISTINE (707)
ETOPOSIDE (670)
Which BEVACIZUMAB-AWWB Alternatives Have Lower Therapy partial responder Risk?
BEVACIZUMAB-AWWB vs BEVACIZUMAB-BVZR
BEVACIZUMAB-AWWB vs BEVACIZUMAB-MALY
BEVACIZUMAB-AWWB vs BEXAROTENE
BEVACIZUMAB-AWWB vs BEZAFIBRATE
BEVACIZUMAB-AWWB vs BEZLOTOXUMAB