Intron a and Shock - a phase IV clinical study of FDA data
Summary:
Shock 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 Shock 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 Shock?
Shock (a life-threatening condition with symptoms like low blood pressure, weakness, shallow breathing, cold, clammy skin) is found to be associated with 1,222 drugs and 1,753 conditions by eHealthMe. Check the latest studies of Shock.
9,303 people reported to have side effects when taking Intron a.
Among them, 14 people (0.15%) have Shock.

Among these 14 people:
How long have people been on Intron a when they have Shock? *
- < 1 month: 90 %
- 1 - 6 months: 10 %
- 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 Shock when taking Intron a? *
- female: 23.08 %
- male: 76.92 %
What is the age of people who have Shock when taking Intron a? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 7.14 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 21.43 %
- 60+: 71.43 %
What are other drugs people take besides Intron a? *
- Rebetol: 7 people, 50.00%
- Ursodiol: 4 people, 28.57%
- Adalat: 2 people, 14.29%
- Vitamins: 1 person, 7.14%
- Silymarin: 1 person, 7.14%
- Pravastatin Sodium: 1 person, 7.14%
- Misoprostol: 1 person, 7.14%
- Lentinan: 1 person, 7.14%
- Famotidine: 1 person, 7.14%
- Diclofenac Sodium: 1 person, 7.14%
What are other side effects people have besides Shock? *
- Thrombocytopenia (decrease of platelets in blood): 6 people, 42.86%
- Pulmonary Haemorrhage (acute bleeding from the lung): 4 people, 28.57%
- Hypotension (abnormally low blood pressure): 3 people, 21.43%
- Coughing Up Blood: 3 people, 21.43%
- Malaise (a feeling of general discomfort or uneasiness): 3 people, 21.43%
- Fever: 2 people, 14.29%
- Multi-Organ Failure (multisystem organ failure): 2 people, 14.29%
- Haemoglobin Decreased: 2 people, 14.29%
- Blood Bilirubin Increased: 2 people, 14.29%
- Drug Ineffective: 2 people, 14.29%
What are the existing conditions these people have? *
- Hepatitis C: 6 people, 42.86%
- Hodgkin's Lymphoma (cancer originating from white blood cells): 1 person, 7.14%
- Chronic Hepatitis (long lasting inflammation of liver): 1 person, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Intron a and have Shock?
- Check whether Shock 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)
Shock treatments and more:
- Shock (28,534 reports)
How severe was Shock 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 Shock:
- Shock (1,222 drugs)
Browse all the conditions that are associated with Shock:
- Shock (1,753 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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