Leflunomide and Takayasu's arteritis - a phase IV clinical study of FDA data
Summary:
Takayasu's arteritis is reported as a side effect among people who take Leflunomide (leflunomide), especially for people who are 30-39 old, also take Azathioprine,.
The phase IV clinical study analyzes which people have Takayasu's arteritis when taking Leflunomide. It is created by eHealthMe based on reports of 81,713 people who have side effects when taking Leflunomide from the FDA, and is updated regularly.
What is Leflunomide?
Leflunomide has active ingredients of leflunomide. It is often used in rheumatoid arthritis. eHealthMe is studying from 82,105 Leflunomide users. Check the latest studies of Leflunomide.
What is Takayasu's arteritis?
Takayasu's arteritis (an inflammation of the aorta -- the artery that carries blood from the heart to the rest of the body) is found to be associated with 67 drugs and 270 conditions by eHealthMe. Check the latest studies of Takayasu's arteritis.
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 >>>.
81,713 people reported to have side effects when taking Leflunomide.
Among them, 24 people (0.03%) have Takayasu's arteritis.

Among these 24 people:
What is the age of people who have Takayasu's arteritis when taking Leflunomide? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 6.67 %
- 30-39: 73.33 %
- 40-49: 6.67 %
- 50-59: 0.0 %
- 60+: 13.33 %
What are other drugs people take besides Leflunomide? *
- Azathioprine: 17 people, 70.83%
- Methotrexate: 16 people, 66.67%
- Prednisone: 10 people, 41.67%
- Actemra: 3 people, 12.50%
- Zantac: 2 people, 8.33%
- Asa: 2 people, 8.33%
- Hyrimoz: 2 people, 8.33%
- Lipitor: 2 people, 8.33%
- Zopiclone: 2 people, 8.33%
- Omega 3: 2 people, 8.33%
What are other side effects people have besides Takayasu's arteritis? *
- Vascular Stenosis (abnormal narrowing blood vessels): 7 people, 29.17%
- Drug Ineffective: 4 people, 16.67%
- Neuropathy Peripheral (surface nerve damage): 2 people, 8.33%
- Heart Rate Irregular: 2 people, 8.33%
- C-Reactive Protein Increased: 2 people, 8.33%
- White Blood Cell Count Decreased: 1 person, 4.17%
- Weight Loss: 1 person, 4.17%
- Weight Increased: 1 person, 4.17%
- Stroke (sudden death of a portion of the brain cells due to a lack of oxygen): 1 person, 4.17%
- Sinusitis (inflammation of sinus): 1 person, 4.17%
* Approximation only. Some reports may have incomplete information.
Do you take Leflunomide and have Takayasu's arteritis?
- Check whether Takayasu's arteritis 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 Leflunomide:
- Leflunomide (82,105 reports)
Takayasu's arteritis treatments and more:
- Takayasu's arteritis (1,800 reports)
How severe was Takayasu's arteritis and when was it recovered:
Expand to all the drugs that have ingredients of leflunomide:
Sub-studies by age:
0-1 2-9 10-19 20-29 30-39 40-49 50-59 60+
Browse all side effects of Leflunomide:
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 Takayasu's arteritis:
- Takayasu's arteritis (67 drugs)
Browse all the conditions that are associated with Takayasu's arteritis:
- Takayasu's arteritis (270 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on leflunomide (the active ingredients of Leflunomide) and Leflunomide (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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