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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 Cause Performance status decreased? 103 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 103 reports of Performance status decreased have been filed in association with BEVACIZUMAB (JOBEVNE). This represents 0.1% of all adverse event reports for BEVACIZUMAB.

103
Reports of Performance status decreased with BEVACIZUMAB
0.1%
of all BEVACIZUMAB reports
37
Deaths
45
Hospitalizations

How Dangerous Is Performance status decreased From BEVACIZUMAB?

Of the 103 reports, 37 (35.9%) resulted in death, 45 (43.7%) required hospitalization, and 2 (1.9%) were considered life-threatening.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB. However, 103 reports have been filed with the FAERS database.

What Other Side Effects Does BEVACIZUMAB Cause?

Off label use (12,094) Death (8,493) Diarrhoea (4,911) Disease progression (4,653) Fatigue (4,572) Nausea (4,357) Hypertension (4,309) Anaemia (3,221) Vomiting (3,193) Neutropenia (2,875)

What Other Drugs Cause Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) CAPECITABINE (75) NIRAPARIB (75) LUMATEPERONE (68) NIVOLUMAB (65)

Which BEVACIZUMAB Alternatives Have Lower Performance status decreased Risk?

BEVACIZUMAB vs BEVACIZUMAB-AWWB BEVACIZUMAB vs BEVACIZUMAB-BVZR BEVACIZUMAB vs BEVACIZUMAB-MALY BEVACIZUMAB vs BEXAROTENE BEVACIZUMAB vs BEYAZ

Related Pages

BEVACIZUMAB Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased BEVACIZUMAB Demographics