Intron a and Renal disorder - a phase IV clinical study of FDA data

Summary:

Renal disorder is reported as a side effect among people who take Intron a (interferon alfa-2b), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Rebetol, and have Hepatitis c.

The phase IV clinical study analyzes which people have Renal disorder when taking Intron a. It is created by eHealthMe based on reports of 9,303 people who have side effects when taking Intron a from the FDA, and is updated regularly.

What is Intron a?

Intron a has active ingredients of interferon alfa-2b. eHealthMe is studying from 9,320 Intron a users. Check the latest studies of Intron a.

What is Renal disorder?

Renal disorder (kidney disease) is found to be associated with 1,719 drugs and 1,671 conditions by eHealthMe. Check the latest studies of Renal disorder.

eHealthMe: drug outcomes in the real world

eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.

On Aug, 30, 2026

9,303 people reported to have side effects when taking Intron a.
Among them, 21 people (0.23%) have Renal disorder.

Among these 21 people:

How long have people been on Intron a when they have Renal disorder? *

What is the gender of people who have Renal disorder when taking Intron a? *

female: 25 %
male: 75 %

What is the age of people who have Renal disorder when taking Intron a? *

What are other drugs people take besides Intron a? *

What are other side effects people have besides Renal disorder? *

Malaise (a feeling of general discomfort or uneasiness): 5 people, 23.81%
Liver Disorder (liver diseases): 5 people, 23.81%
Sepsis (a severe blood infection that can lead to organ failure and death): 4 people, 19.05%
Hepatic Failure (liver failure): 4 people, 19.05%
Hypotension (abnormally low blood pressure): 3 people, 14.29%
Fatigue (feeling of tiredness): 3 people, 14.29%
Impaired Work Ability: 2 people, 9.52%
Mental Disorder (a psychological term for a mental or behavioural pattern or anomaly that causes distress or disability): 2 people, 9.52%
Loss Of Consciousness: 2 people, 9.52%
Heart Attack: 2 people, 9.52%

What are the existing conditions these people have? *

Hepatitis C: 8 people, 38.10%
Renal Cell Carcinoma (a kidney cancer): 4 people, 19.05%
Polycythemia Vera (blood disorder in which the bone marrow makes too many red blood cells): 1 person, 4.76%
Malignant Melanoma (skin cancer rises from melancytes): 1 person, 4.76%
Iron Overload: 1 person, 4.76%
High Blood Pressure: 1 person, 4.76%

* Approximation only. Some reports may have incomplete information.

Do you take Intron a and have Renal disorder?

- Check whether Renal disorder 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 Intron a:

Intron a (9,320 reports)

Renal disorder treatments and more:

Renal disorder (60,733 reports)

Browse all side effects of Intron a:

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 z

Browse all the drugs that are associated with Renal disorder:

Renal disorder (1,719 drugs)

Browse all the conditions that are associated with Renal disorder:

Renal disorder (1,671 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on interferon alfa-2b (the active ingredients of Intron a) and Intron a (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.