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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 CETUXIMAB Cause Post procedural haemorrhage? 15 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 15 reports of Post procedural haemorrhage have been filed in association with CETUXIMAB (ERBITUX). This represents 0.1% of all adverse event reports for CETUXIMAB.

15
Reports of Post procedural haemorrhage with CETUXIMAB
0.1%
of all CETUXIMAB reports
1
Deaths
6
Hospitalizations

How Dangerous Is Post procedural haemorrhage From CETUXIMAB?

Of the 15 reports, 1 (6.7%) resulted in death, 6 (40.0%) required hospitalization, and 1 (6.7%) were considered life-threatening.

Is Post procedural haemorrhage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for CETUXIMAB. However, 15 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 Post procedural haemorrhage?

LEVONORGESTREL (1,106) RIVAROXABAN (930) ASPIRIN (618) APIXABAN (539) ADALIMUMAB (476) IBRUTINIB (269) CLOPIDOGREL BISULFATE (235) HEPARIN (174) WARFARIN (170) DABIGATRAN ETEXILATE (121)

Which CETUXIMAB Alternatives Have Lower Post procedural haemorrhage Risk?

CETUXIMAB vs CETYLPYRIDINIUM CETUXIMAB vs CEVIMELINE CETUXIMAB vs CHAMPIX CETUXIMAB vs CHANTIX CETUXIMAB vs CHENODIOL

Related Pages

CETUXIMAB Full Profile All Post procedural haemorrhage Reports All Drugs Causing Post procedural haemorrhage CETUXIMAB Demographics