Does CETUXIMAB Cause Condition aggravated? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Condition aggravated have been filed in association with CETUXIMAB (ERBITUX). This represents 0.6% of all adverse event reports for CETUXIMAB.
84
Reports of Condition aggravated with CETUXIMAB
0.6%
of all CETUXIMAB reports
18
Deaths
40
Hospitalizations
How Dangerous Is Condition aggravated From CETUXIMAB?
Of the 84 reports, 18 (21.4%) resulted in death, 40 (47.6%) required hospitalization, and 8 (9.5%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CETUXIMAB. However, 84 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CETUXIMAB Alternatives Have Lower Condition aggravated Risk?
CETUXIMAB vs CETYLPYRIDINIUM
CETUXIMAB vs CEVIMELINE
CETUXIMAB vs CHAMPIX
CETUXIMAB vs CHANTIX
CETUXIMAB vs CHENODIOL