Does CETUXIMAB Cause Haemoglobin decreased? 85 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 85 reports of Haemoglobin decreased have been filed in association with CETUXIMAB (ERBITUX). This represents 0.6% of all adverse event reports for CETUXIMAB.
85
Reports of Haemoglobin decreased with CETUXIMAB
0.6%
of all CETUXIMAB reports
13
Deaths
49
Hospitalizations
How Dangerous Is Haemoglobin decreased From CETUXIMAB?
Of the 85 reports, 13 (15.3%) resulted in death, 49 (57.6%) required hospitalization, and 6 (7.1%) 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 CETUXIMAB. However, 85 reports have been filed with the FAERS database.
What Other Side Effects Does CETUXIMAB Cause?
Off label use (1,549)
Rash (883)
Diarrhoea (874)
Neutropenia (744)
Nausea (663)
Malignant neoplasm progression (662)
Dyspnoea (542)
Decreased appetite (541)
Vomiting (533)
Death (518)
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 CETUXIMAB Alternatives Have Lower Haemoglobin decreased Risk?
CETUXIMAB vs CETYLPYRIDINIUM
CETUXIMAB vs CEVIMELINE
CETUXIMAB vs CHAMPIX
CETUXIMAB vs CHANTIX
CETUXIMAB vs CHENODIOL