Ultravist and Type iv hypersensitivity reaction - a phase IV clinical study of FDA data
Summary:
Type iv hypersensitivity reaction is reported as a side effect among people who take Ultravist (iopromide), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Candesartan Cilexetil, and have Computerised tomogram abdomen.
The phase IV clinical study analyzes which people have Type iv hypersensitivity reaction when taking Ultravist. It is created by eHealthMe based on reports of 9,241 people who have side effects when taking Ultravist from the FDA, and is updated regularly.
What is Ultravist?
Ultravist has active ingredients of iopromide. eHealthMe is studying from 9,246 Ultravist users. Check the latest studies of Ultravist.
What is Type iv hypersensitivity reaction?
Type iv hypersensitivity reaction (delayed type hypersensitivity as the reaction takes two to three days to develop) is found to be associated with 193 drugs and 415 conditions by eHealthMe. Check the latest studies of Type iv hypersensitivity reaction.
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 >>>.
9,241 people reported to have side effects when taking Ultravist.
Among them, 13 people (0.14%) have Type iv hypersensitivity reaction.

Among these 13 people:
How long have people been on Ultravist when they have Type iv hypersensitivity reaction? *
- < 1 month: 100 %
- 1 - 6 months: 0.0 %
- 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 Type iv hypersensitivity reaction when taking Ultravist? *
- female: 38.46 %
- male: 61.54 %
What is the age of people who have Type iv hypersensitivity reaction when taking Ultravist? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 15.38 %
- 30-39: 0.0 %
- 40-49: 15.38 %
- 50-59: 15.38 %
- 60+: 53.85 %
What are other drugs people take besides Ultravist? *
- Plavix: 4 people, 30.77%
- Candesartan Cilexetil: 4 people, 30.77%
What are other side effects people have besides Type iv hypersensitivity reaction? *
- Ventricular Fibrillation (abnormally irregular heart rhythm): 4 people, 30.77%
- Rhabdomyolysis (a condition in which damaged skeletal muscle tissue breaks down): 4 people, 30.77%
- Itching: 3 people, 23.08%
- Weight Bearing Difficulty (difficulty due to weight of thigh fat deposition): 2 people, 15.38%
- Joint Pain: 2 people, 15.38%
- Arthropathy: 2 people, 15.38%
- Balance Disorder: 2 people, 15.38%
- Blister (small pocket of fluid within the upper layers of the skin caused by forceful rubbing (friction), burning, freezing, chemical exposure): 2 people, 15.38%
- Dermatitis Exfoliative Generalised (inflammatory skin disease with erythema and scaling that affects nearly the entire cutaneous surface): 2 people, 15.38%
- Drug Eruption (adverse drug reaction of the skin): 2 people, 15.38%
What are the existing conditions these people have? *
- Computerised Tomogram Abdomen: 1 person, 7.69%
* Approximation only. Some reports may have incomplete information.
Do you take Ultravist and have Type iv hypersensitivity reaction?
- Check whether Type iv hypersensitivity reaction 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 Ultravist:
- Ultravist (9,246 reports)
Type iv hypersensitivity reaction treatments and more:
- Type iv hypersensitivity reaction (2,728 reports)
How severe was Type iv hypersensitivity reaction and when was it recovered:
Expand to all the drugs that have ingredients of iopromide:
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 Ultravist:
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 Type iv hypersensitivity reaction:
- Type iv hypersensitivity reaction (194 drugs)
Browse all the conditions that are associated with Type iv hypersensitivity reaction:
- Type iv hypersensitivity reaction (415 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on iopromide (the active ingredients of Ultravist) and Ultravist (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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