Does BEVACIZUMAB Cause Haemoglobin decreased? 616 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 616 reports of Haemoglobin decreased have been filed in association with BEVACIZUMAB (JOBEVNE). This represents 0.8% of all adverse event reports for BEVACIZUMAB.
616
Reports of Haemoglobin decreased with BEVACIZUMAB
0.8%
of all BEVACIZUMAB reports
101
Deaths
313
Hospitalizations
How Dangerous Is Haemoglobin decreased From BEVACIZUMAB?
Of the 616 reports, 101 (16.4%) resulted in death, 313 (50.8%) required hospitalization, and 53 (8.6%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEVACIZUMAB. However, 616 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which BEVACIZUMAB Alternatives Have Lower Haemoglobin decreased Risk?
BEVACIZUMAB vs BEVACIZUMAB-AWWB
BEVACIZUMAB vs BEVACIZUMAB-BVZR
BEVACIZUMAB vs BEVACIZUMAB-MALY
BEVACIZUMAB vs BEXAROTENE
BEVACIZUMAB vs BEYAZ