Erbitux and Hypertransaminasaemia - a phase IV clinical study of FDA data
Summary:
Hypertransaminasaemia is reported as a side effect among people who take Erbitux (cetuximab), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Fluorouracil, and have Cancer - throat or larynx.
The phase IV clinical study analyzes which people have Hypertransaminasaemia when taking Erbitux. It is created by eHealthMe based on reports of 19,227 people who have side effects when taking Erbitux from the FDA, and is updated regularly.
What is Erbitux?
Erbitux has active ingredients of cetuximab. It is often used in cancer. eHealthMe is studying from 19,276 Erbitux users. Check the latest studies of Erbitux.
What is Hypertransaminasaemia?
Hypertransaminasaemia is found to be associated with 358 drugs and 395 conditions by eHealthMe. Check the latest studies of Hypertransaminasaemia.
19,227 people reported to have side effects when taking Erbitux.
Among them, 15 people (0.08%) have Hypertransaminasaemia.

Among these 15 people:
How long have people been on Erbitux when they have Hypertransaminasaemia? *
- < 1 month: 71.43 %
- 1 - 6 months: 28.57 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Hypertransaminasaemia when taking Erbitux? *
- female: 64.29 %
- male: 35.71 %
What is the age of people who have Hypertransaminasaemia when taking Erbitux? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 28.57 %
- 60+: 71.43 %
What are other drugs people take besides Erbitux? *
- Fluorouracil: 5 people, 33.33%
- Leucovorin Calcium: 2 people, 13.33%
- Irinotecan Hydrochloride: 2 people, 13.33%
- Camptosar: 2 people, 13.33%
What are other side effects people have besides Hypertransaminasaemia? *
- Nausea (feeling of having an urge to vomit): 7 people, 46.67%
- Hyperbilirubinaemia (excess of bilirubin in the blood): 4 people, 26.67%
- Dry Skin: 4 people, 26.67%
- Indigestion: 3 people, 20.00%
- Hypersensitivity: 3 people, 20.00%
- Folliculitis (infection of hair root): 3 people, 20.00%
- Febrile Neutropenia (fever with reduced white blood cells): 3 people, 20.00%
- Diarrhea: 3 people, 20.00%
- Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection): 3 people, 20.00%
- Infusion Related Reaction: 2 people, 13.33%
What are the existing conditions these people have? *
- Rectal Cancer (cancer of rectum): 4 people, 26.67%
- Cancer - Throat Or Larynx: 4 people, 26.67%
- Rectal Cancer Metastatic (cancer of rectum spreads to other): 2 people, 13.33%
- Colon Cancer: 1 person, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Erbitux and have Hypertransaminasaemia?
- Check whether Hypertransaminasaemia is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, long term effects of, and alternative drugs to Erbitux:
- Erbitux (19,276 reports)
Hypertransaminasaemia treatments and more:
- Hypertransaminasaemia (5,236 reports)
How severe was Hypertransaminasaemia and when was it recovered:
Expand to all the drugs that have ingredients of cetuximab:
Sub-studies by gender and age:
Female: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Male: 0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Erbitux:
a b c d e f g h i j k l m n o p q r s t u v w x y zBrowse all the drugs that are associated with Hypertransaminasaemia:
- Hypertransaminasaemia (358 drugs)
Browse all the conditions that are associated with Hypertransaminasaemia:
- Hypertransaminasaemia (395 conditions)
Related publications that referenced our studies
- Gupta D, Shukla P, Bisht SS, Bhatt ML, Pant MC, Srivastava K, "Deep vein and artery thrombosis associated with cetuximab-based chemoradiotherapy", Indian journal of pharmacology, 2011 Jan .
- Gupta D, Shukla P, Bisht SS, Bhatt ML, Pant MC, Srivastava K, "Deep vein and artery thrombosis associated with cetuximab-based chemoradiotherapy", Indian journal of pharmacology, 2011 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on cetuximab (the active ingredients of Erbitux) and Erbitux (the brand name). Other drugs that have the same active ingredients (e.g. generic drugs) are not considered. Dosage of drugs is not considered in the study.
How to use the study?
DO NOT STOP MEDICATIONS without first consulting your doctor. If there are any serious or long term adverse effects discovered in the study, discuss the study with your doctor to ensure that proper medication management will be in place if applicable.
Who is eHealthMe?
With medical big data and proven AI/ML algorithms, eHealthMe provides a platform for everyone to run phase IV clinical trials. We study millions of patients and 5,000 more each day. Results of our real-world drug study have been referenced on 800+ peer-reviewed medical publications, including The Lancet, Mayo Clinic Proceedings, and Nature. Our analysis results are available to researchers, health care professionals, patients (testimonials), and software developers (open API).
WARNING, DISCLAIMER, USE FOR PUBLICATION
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only. Our phase IV clinical studies alone cannot establish cause-effect relationship. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.
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