Victrelis and Hepatitis cholestatic - a phase IV clinical study of FDA data
Summary:
Hepatitis cholestatic is reported as a side effect among people who take Victrelis (boceprevir), especially for people who are female, 30-39 old, also take Intron A, and have Immunodeficiency disorders.
The phase IV clinical study analyzes which people have Hepatitis cholestatic when taking Victrelis. It is created by eHealthMe based on reports of 8,612 people who have side effects when taking Victrelis from the FDA, and is updated regularly.
What is Victrelis?
Victrelis has active ingredients of boceprevir. It is often used in hepatitis c. eHealthMe is studying from 8,634 Victrelis users. Check the latest studies of Victrelis.
What is Hepatitis cholestatic?
Hepatitis cholestatic (flow of bile from the liver is slowed or blocked) is found to be associated with 543 drugs and 824 conditions by eHealthMe. Check the latest studies of Hepatitis cholestatic.
8,612 people reported to have side effects when taking Victrelis.
Among them, 14 people (0.16%) have Hepatitis cholestatic.

Among these 14 people:
What is the gender of people who have Hepatitis cholestatic when taking Victrelis? *
- female: 100 %
- male: 0.0 %
What is the age of people who have Hepatitis cholestatic when taking Victrelis? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 100 %
- 40-49: 0.0 %
- 50-59: 0.0 %
- 60+: 0.0 %
What are other drugs people take besides Victrelis? *
- Prograf: 13 people, 92.86%
- Intron A: 13 people, 92.86%
- Pegasys: 10 people, 71.43%
- Mycophenolate Mofetil: 2 people, 14.29%
- Tacrolimus: 1 person, 7.14%
- Ribavirin: 1 person, 7.14%
What are other side effects people have besides Hepatitis cholestatic? *
- Ascites (accumulation of fluid in the abdominal cavity): 14 people, 100.00%
- Anaemia (lack of blood): 14 people, 100.00%
- Agranulocytosis (a deficiency of granulocytes in the blood, causing increased vulnerability to infection): 14 people, 100.00%
- Drug Level Increased: 13 people, 92.86%
- Drug Ineffective: 13 people, 92.86%
- Renal Impairment (severely reduced kidney function): 11 people, 78.57%
- Jaundice - Yellow Skin (a yellowish pigmentation of the skin): 11 people, 78.57%
- Hepatic Function Abnormal: 11 people, 78.57%
- Hepatic Enzyme Increased: 11 people, 78.57%
- Immunosuppressant Drug Level Increased: 1 person, 7.14%
What are the existing conditions these people have? *
- Shunt Thrombosis (blood clotting at shunt): 6 people, 42.86%
- Immunodeficiency Disorders: 6 people, 42.86%
* Approximation only. Some reports may have incomplete information.
Do you take Victrelis and have Hepatitis cholestatic?
- Check whether Hepatitis cholestatic 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 Victrelis:
- Victrelis (8,634 reports)
Hepatitis cholestatic treatments and more:
- Hepatitis cholestatic (7,775 reports)
How severe was Hepatitis cholestatic and when was it recovered:
Expand to all the drugs that have ingredients of boceprevir:
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 Victrelis:
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 Hepatitis cholestatic:
- Hepatitis cholestatic (543 drugs)
Browse all the conditions that are associated with Hepatitis cholestatic:
- Hepatitis cholestatic (824 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on boceprevir (the active ingredients of Victrelis) and Victrelis (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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