Medrol and Wound secretion - a phase IV clinical study of FDA data

Summary:

Wound secretion is reported as a side effect among people who take Medrol (methylprednisolone), especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months also take Neoral, and have High blood pressure.

The phase IV clinical study analyzes which people have Wound secretion when taking Medrol. It is created by eHealthMe based on reports of 23,951 people who have side effects when taking Medrol from the FDA, and is updated regularly.

What is Medrol?

Medrol has active ingredients of methylprednisolone. It is often used in rheumatoid arthritis. eHealthMe is studying from 24,443 Medrol users. Check the latest studies of Medrol.

What is Wound secretion?

Wound secretion is found to be associated with 571 drugs and 761 conditions by eHealthMe. Check the latest studies of Wound secretion.

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, 17, 2026

23,951 people reported to have side effects when taking Medrol.
Among them, 38 people (0.16%) have Wound secretion.

Among these 38 people:

How long have people been on Medrol when they have Wound secretion? *

What is the gender of people who have Wound secretion when taking Medrol? *

female: 90.91 %
male: 9.09 %

What is the age of people who have Wound secretion when taking Medrol? *

What are other drugs people take besides Medrol? *

What are other side effects people have besides Wound secretion? *

Fatigue (feeling of tiredness): 17 people, 44.74%
Fever: 16 people, 42.11%
Infection: 16 people, 42.11%
Urinary Tract Infection: 15 people, 39.47%
Headache (pain in head): 15 people, 39.47%
Joint Pain: 14 people, 36.84%
Aseptic Necrosis (the death of bone tissue due to a lack of blood supply): 12 people, 31.58%
Gait Disturbance: 12 people, 31.58%
Fall: 12 people, 31.58%
Bone Disorder: 11 people, 28.95%

What are the existing conditions these people have? *

High Blood Pressure: 12 people, 31.58%
Primary Myelofibrosis (primary disorder of the bone marrow): 5 people, 13.16%
Polycythaemia Vera (blood disorder in which the bone marrow makes too many red blood cells): 5 people, 13.16%
Uveitis (inflammation of the uvea): 4 people, 10.53%
Juvenile Rheumatoid Arthritis (joint inflammation in children due to systemic disease): 4 people, 10.53%
Allergic Rhinitis: 4 people, 10.53%
Anaemia (lack of blood): 4 people, 10.53%
Genital Rash (rash on sex organ): 4 people, 10.53%
Abdominal Pain: 4 people, 10.53%
Psoriasis (immune-mediated disease that affects the skin): 4 people, 10.53%

* Approximation only. Some reports may have incomplete information.

Do you take Medrol and have Wound secretion?

- Check whether Wound secretion 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 Medrol:

Medrol (24,443 reports)

Wound secretion treatments and more:

Wound secretion (5,127 reports)

Browse all side effects of Medrol:

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 Wound secretion:

Wound secretion (571 drugs)

Browse all the conditions that are associated with Wound secretion:

Wound secretion (761 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on methylprednisolone (the active ingredients of Medrol) and Medrol (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.