Does BEVACIZUMAB-AWWB Cause Product storage error? 437 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 437 reports of Product storage error have been filed in association with BEVACIZUMAB-AWWB. This represents 10.6% of all adverse event reports for BEVACIZUMAB-AWWB.
437
Reports of Product storage error with BEVACIZUMAB-AWWB
10.6%
of all BEVACIZUMAB-AWWB reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product storage error From BEVACIZUMAB-AWWB?
Of the 437 reports.
Is Product storage error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB-AWWB. However, 437 reports have been filed with the FAERS database.
What Other Side Effects Does BEVACIZUMAB-AWWB Cause?
Off label use (441)
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)
Intercepted product administration error (97)
What Other Drugs Cause Product storage error?
INSULIN GLARGINE (7,743)
EVOLOCUMAB (6,606)
ETANERCEPT (3,653)
DENOSUMAB (3,621)
ERENUMAB-AOOE (2,958)
DUPILUMAB (2,631)
ALBUTEROL (2,474)
ABATACEPT (2,101)
DARBEPOETIN ALFA (1,619)
INSULIN LISPRO (1,448)
Which BEVACIZUMAB-AWWB Alternatives Have Lower Product storage error Risk?
BEVACIZUMAB-AWWB vs BEVACIZUMAB-BVZR
BEVACIZUMAB-AWWB vs BEVACIZUMAB-MALY
BEVACIZUMAB-AWWB vs BEXAROTENE
BEVACIZUMAB-AWWB vs BEZAFIBRATE
BEVACIZUMAB-AWWB vs BEZLOTOXUMAB