Intron a and Dermatitis - atopic - a phase IV clinical study of FDA data
Summary:
Dermatitis - atopic is reported as a side effect among people who take Intron a (interferon alfa-2b), especially for people who are male, 30-39 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 Dermatitis - atopic 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 Dermatitis - atopic?
Dermatitis - atopic (inflammatory, chronically relapsing, non-contagious and pruritic skin disorder) is found to be associated with 2,026 drugs and 1,971 conditions by eHealthMe. Check the latest studies of Dermatitis - atopic.
9,303 people reported to have side effects when taking Intron a.
Among them, 16 people (0.17%) have Dermatitis - atopic.

Among these 16 people:
How long have people been on Intron a when they have Dermatitis - atopic? *
- < 1 month: 66.67 %
- 1 - 6 months: 33.33 %
- 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 Dermatitis - atopic when taking Intron a? *
- female: 33.33 %
- male: 66.67 %
What is the age of people who have Dermatitis - atopic when taking Intron a? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 42.86 %
- 40-49: 35.71 %
- 50-59: 7.14 %
- 60+: 14.29 %
What are other drugs people take besides Intron a? *
- Rebetol: 10 people, 62.50%
- Famotidine: 3 people, 18.75%
- Diclofenac Sodium: 3 people, 18.75%
- Theo-24: 1 person, 6.25%
- Tamoxifen Citrate: 1 person, 6.25%
- Synthroid: 1 person, 6.25%
What are other side effects people have besides Dermatitis - atopic? *
- Itching: 5 people, 31.25%
- Weight Decreased: 5 people, 31.25%
- Skin Discoloration: 3 people, 18.75%
- Porphyrinuria (presence of porphyrin in the urine): 3 people, 18.75%
- Blood Iron Increased: 2 people, 12.50%
- Eosinophil Count Increased: 2 people, 12.50%
- Influenza Like Illness: 2 people, 12.50%
- Hyperkeratosis (thickening of the outer layer of the skin): 1 person, 6.25%
- Dry Mouth: 1 person, 6.25%
- Dry Skin: 1 person, 6.25%
What are the existing conditions these people have? *
- Hepatitis C: 4 people, 25.00%
- Malignant Melanoma (skin cancer rises from melancytes): 1 person, 6.25%
- Chronic Hepatitis (long lasting inflammation of liver): 1 person, 6.25%
* Approximation only. Some reports may have incomplete information.
Do you take Intron a and have Dermatitis - atopic?
- Check whether Dermatitis - atopic 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)
Dermatitis - atopic treatments and more:
- Dermatitis - atopic (61,311 reports)
How severe was Dermatitis - atopic and when was it recovered:
Expand to all the drugs that have ingredients of interferon alfa-2b:
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 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 zBrowse all the drugs that are associated with Dermatitis - atopic:
- Dermatitis - atopic (2,026 drugs)
Browse all the conditions that are associated with Dermatitis - atopic:
- Dermatitis - atopic (1,971 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.
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