Does BEVACIZUMAB-AWWB Cause Intercepted product administration error? 97 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 97 reports of Intercepted product administration error have been filed in association with BEVACIZUMAB-AWWB. This represents 2.3% of all adverse event reports for BEVACIZUMAB-AWWB.
97
Reports of Intercepted product administration error with BEVACIZUMAB-AWWB
2.3%
of all BEVACIZUMAB-AWWB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Intercepted product administration error From BEVACIZUMAB-AWWB?
Of the 97 reports.
Is Intercepted product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB-AWWB. However, 97 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 Intercepted product administration error?
EVOLOCUMAB (2,508)
DENOSUMAB (1,209)
ERENUMAB-AOOE (1,015)
ETANERCEPT (574)
DARBEPOETIN ALFA (385)
PEGFILGRASTIM (356)
LEUPROLIDE (307)
ERYTHROPOIETIN (301)
ROMOSOZUMAB-AQQG (115)
BENZYL ALCOHOL\ETANERCEPT (112)
Which BEVACIZUMAB-AWWB Alternatives Have Lower Intercepted product administration error Risk?
BEVACIZUMAB-AWWB vs BEVACIZUMAB-BVZR
BEVACIZUMAB-AWWB vs BEVACIZUMAB-MALY
BEVACIZUMAB-AWWB vs BEXAROTENE
BEVACIZUMAB-AWWB vs BEZAFIBRATE
BEVACIZUMAB-AWWB vs BEZLOTOXUMAB