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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does BEVACIZUMAB-AWWB Cause Product preparation error? 62 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 62 reports of Product preparation error have been filed in association with BEVACIZUMAB-AWWB. This represents 1.5% of all adverse event reports for BEVACIZUMAB-AWWB.

62
Reports of Product preparation error with BEVACIZUMAB-AWWB
1.5%
of all BEVACIZUMAB-AWWB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product preparation error From BEVACIZUMAB-AWWB?

Of the 62 reports.

Is Product preparation error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB-AWWB. However, 62 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 Product preparation error?

ONABOTULINUMTOXINA (3,593) EVOLOCUMAB (2,785) DUPILUMAB (2,707) BUPRENORPHINE\NALOXONE (777) ABOBOTULINUMTOXINA (751) ALBIGLUTIDE (691) ALBUTEROL (520) PEGFILGRASTIM (473) ALIROCUMAB (402) LEUPROLIDE (400)

Which BEVACIZUMAB-AWWB Alternatives Have Lower Product preparation error Risk?

BEVACIZUMAB-AWWB vs BEVACIZUMAB-BVZR BEVACIZUMAB-AWWB vs BEVACIZUMAB-MALY BEVACIZUMAB-AWWB vs BEXAROTENE BEVACIZUMAB-AWWB vs BEZAFIBRATE BEVACIZUMAB-AWWB vs BEZLOTOXUMAB

Related Pages

BEVACIZUMAB-AWWB Full Profile All Product preparation error Reports All Drugs Causing Product preparation error BEVACIZUMAB-AWWB Demographics