Voltaren and Application site reaction - a phase IV clinical study of FDA data
Summary:
Application site reaction is reported as a side effect among people who take Voltaren (diclofenac sodium), especially for people who are female, 60+ old, have been taking the drug for < 1 month also take Celebrex, and have Back pain.
The phase IV clinical study analyzes which people have Application site reaction when taking Voltaren. It is created by eHealthMe based on reports of 81,356 people who have side effects when taking Voltaren from the FDA, and is updated regularly.
What is Voltaren?
Voltaren has active ingredients of diclofenac sodium. It is often used in arthritis. eHealthMe is studying from 82,346 Voltaren users. Check the latest studies of Voltaren.
What is Application site reaction?
Application site reaction is found to be associated with 377 drugs and 550 conditions by eHealthMe. Check the latest studies of Application site 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 >>>.
81,356 people reported to have side effects when taking Voltaren.
Among them, 61 people (0.07%) have Application site reaction.

Among these 61 people:
How long have people been on Voltaren when they have Application site reaction? *
- < 1 month: 68.18 %
- 1 - 6 months: 22.73 %
- 6 - 12 months: 4.55 %
- 1 - 2 years: 4.55 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Application site reaction when taking Voltaren? *
- female: 67.27 %
- male: 32.73 %
What is the age of people who have Application site reaction when taking Voltaren? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 2.17 %
- 20-29: 6.52 %
- 30-39: 4.35 %
- 40-49: 4.35 %
- 50-59: 23.91 %
- 60+: 58.7 %
What are other drugs people take besides Voltaren? *
- Celebrex: 5 people, 8.20%
- Lasix: 2 people, 3.28%
- Oxycontin: 2 people, 3.28%
- Androderm: 2 people, 3.28%
- Duragesic: 2 people, 3.28%
- Fentanyl Transdermal System: 2 people, 3.28%
- Neurontin: 2 people, 3.28%
- Acetylsalicylic Acid: 2 people, 3.28%
- Zantac: 2 people, 3.28%
- Transderm Scop: 2 people, 3.28%
What are other side effects people have besides Application site reaction? *
- Application Site Pruritus (application site severe itching of the skin): 10 people, 16.39%
- Application Site Erythema (redness of the skin at application site): 9 people, 14.75%
- Application Site Pain: 8 people, 13.11%
- Application Site Rash: 6 people, 9.84%
- Rashes (redness): 4 people, 6.56%
- Application Site Papules (solid elevation of skin with no visible fluid at application site): 4 people, 6.56%
- Itching: 4 people, 6.56%
- Rash Macular (small, flat red spots): 3 people, 4.92%
- Skin Discoloration: 3 people, 4.92%
- Application Site Vesicles (small bubble within a cell at application site): 3 people, 4.92%
What are the existing conditions these people have? *
- Joint Pain: 3 people, 4.92%
- Back Pain: 3 people, 4.92%
- Rheumatoid Arthritis (a chronic progressive disease causing inflammation in the joints): 2 people, 3.28%
- High Blood Cholesterol: 2 people, 3.28%
- High Blood Pressure: 2 people, 3.28%
- Muscle Aches (muscle pain): 2 people, 3.28%
- Tendonitis (a condition that causes pain and swelling of tendons): 2 people, 3.28%
- Inflammation: 2 people, 3.28%
- Ulnar Nerve Injury: 1 person, 1.64%
- Aseptic Necrosis (the death of bone tissue due to a lack of blood supply): 1 person, 1.64%
* Approximation only. Some reports may have incomplete information.
Do you take Voltaren and have Application site reaction?
- Check whether Application site 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 Voltaren:
- Voltaren (82,346 reports)
Application site reaction treatments and more:
- Application site reaction (7,439 reports)
How severe was Application site reaction and when was it recovered:
Expand to all the drugs that have ingredients of diclofenac sodium:
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 Voltaren:
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 Application site reaction:
- Application site reaction (377 drugs)
Browse all the conditions that are associated with Application site reaction:
- Application site reaction (550 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on diclofenac sodium (the active ingredients of Voltaren) and Voltaren (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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