Escitalopram and Application site rash - a phase IV clinical study of FDA data

Summary:

Application site rash is reported as a side effect among people who take Escitalopram (escitalopram oxalate), especially for people who are female, 60+ old, also take Gabapentin, and have Pain.

The phase IV clinical study analyzes which people have Application site rash when taking Escitalopram. It is created by eHealthMe based on reports of 75,134 people who have side effects when taking Escitalopram from the FDA, and is updated regularly.

What is Escitalopram?

Escitalopram has active ingredients of escitalopram oxalate. It is often used in depression. eHealthMe is studying from 78,080 Escitalopram users. Check the latest studies of Escitalopram.

What is Application site rash?

Application site rash is found to be associated with 392 drugs and 629 conditions by eHealthMe. Check the latest studies of Application site rash.

On Jul, 19, 2026

75,134 people reported to have side effects when taking Escitalopram.
Among them, 15 people (0.02%) have Application site rash.

Could Escitalopram cause Application site rash?

Among these 15 people:

What is the gender of people who have Application site rash when taking Escitalopram? *

female: 73.33 %
male: 26.67 %

What is the age of people who have Application site rash when taking Escitalopram? *

What are other drugs people take besides Escitalopram? *

What are other side effects people have besides Application site rash? *

Nausea And Vomiting: 6 people, 40.00%
White Blood Cell Count Decreased: 5 people, 33.33%
Drug Dependence: 5 people, 33.33%
Headache (pain in head): 5 people, 33.33%
Haematemesis (vomiting of blood): 5 people, 33.33%
Fatigue (feeling of tiredness): 5 people, 33.33%
Fainting (loss of consciousness and postural tone): 5 people, 33.33%
Ear Pain: 5 people, 33.33%
Drowsiness: 5 people, 33.33%
Hypokalemia (low potassium): 5 people, 33.33%

What are the existing conditions these people have? *

Pain: 5 people, 33.33%
Dementia Alzheimer's Type (loss of mental ability with alzheimer's symptom): 2 people, 13.33%
Actinic Keratosis (skin disease due to sun exposure): 2 people, 13.33%
Type 2 Diabetes: 1 person, 6.67%
Quit Smoking: 1 person, 6.67%
Parkinson's Disease: 1 person, 6.67%
Occipital Neuralgia (a condition characterized by chronic pain in the upper neck): 1 person, 6.67%
High Blood Pressure: 1 person, 6.67%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 1 person, 6.67%
Dementia (madness): 1 person, 6.67%

* Approximation only. Some reports may have incomplete information.

Do you take Escitalopram and have Application site rash?

- Check whether Application site rash 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 Escitalopram:

Escitalopram (78,080 reports)

Browse all side effects of Escitalopram:

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 Application site rash:

Application site rash (392 drugs)

Browse all the conditions that are associated with Application site rash:

Application site rash (629 conditions)

Related publications that referenced our studies

O’Brien FE, O’Connor RM, Clarke G, Donovan MD, Dinan TG, Griffin BT, Cryan JF, "The P-glycoprotein inhibitor cyclosporin A differentially influences behavioural and neurochemical responses to the antidepressant escitalopram", Behavioural brain research, 2014 Mar .
O’Brien FE, O’Connor RM, Clarke G, Donovan MD, Dinan TG, Griffin BT, Cryan JF, "The P-glycoprotein inhibitor cyclosporin A differentially influences behavioural and neurochemical responses to the antidepressant escitalopram", Behavioural brain research, 2014 Mar .

How the study uses the data?

The study uses data from the FDA. It is based on escitalopram oxalate (the active ingredients of Escitalopram) and Escitalopram (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.