Vortioxetine hydrobromide and Hyperhidrosis - a phase IV clinical study of FDA data

Summary:

Hyperhidrosis is reported as a side effect among people who take Vortioxetine hydrobromide (vortioxetine hydrobromide), especially for people who are female, 50-59 old, also take Lyrica, and have Depression.

The phase IV clinical study analyzes which people have Hyperhidrosis when taking Vortioxetine hydrobromide. It is created by eHealthMe based on reports of 302 people who have side effects when taking Vortioxetine hydrobromide from the FDA, and is updated regularly.

What is Vortioxetine hydrobromide?

Vortioxetine hydrobromide has active ingredients of vortioxetine hydrobromide. eHealthMe is studying from 302 Vortioxetine hydrobromide users. Check the latest studies of Vortioxetine hydrobromide.

What is Hyperhidrosis?

Hyperhidrosis (abnormally increased sweating) is found to be associated with 2,546 drugs and 3,546 conditions by eHealthMe. Check the latest studies of Hyperhidrosis.

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, 21, 2026

302 people reported to have side effects when taking Vortioxetine hydrobromide.
Among them, 81 people (26.82%) have Hyperhidrosis.

Could Vortioxetine hydrobromide cause Hyperhidrosis?

Among these 81 people:

What is the gender of people who have Hyperhidrosis when taking Vortioxetine hydrobromide? *

female: 91.67 %
male: 8.33 %

What is the age of people who have Hyperhidrosis when taking Vortioxetine hydrobromide? *

What are other drugs people take besides Vortioxetine hydrobromide? *

What are other side effects people have besides Hyperhidrosis? *

Drowsiness: 80 people, 98.77%
Skin Blushing/flushing (a sudden reddening of the face, neck): 76 people, 93.83%
Nausea (feeling of having an urge to vomit): 76 people, 93.83%
Dizziness: 75 people, 92.59%
Diarrhea: 75 people, 92.59%
Feeling Hot: 75 people, 92.59%
Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 75 people, 92.59%
Headache (pain in head): 75 people, 92.59%
Hostility: 75 people, 92.59%
Nightmares (unpleasant dreams): 75 people, 92.59%

What are the existing conditions these people have? *

Migraine (headache): 74 people, 91.36%
Depression: 74 people, 91.36%
Pain: 30 people, 37.04%
Ulcerative Colitis (inflammatory bowel disease (ibd). it causes swelling, ulcerations, and loss of function of the large intestine): 1 person, 1.23%
Seizures (abnormal excessive or synchronous neuronal activity in the brain): 1 person, 1.23%
Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 1 person, 1.23%

* Approximation only. Some reports may have incomplete information.

Do you take Vortioxetine hydrobromide and have Hyperhidrosis?

- Check whether Hyperhidrosis 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 Vortioxetine hydrobromide:

Vortioxetine hydrobromide (302 reports)

Hyperhidrosis treatments and more:

Hyperhidrosis (147,206 reports)

Browse all side effects of Vortioxetine hydrobromide:

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 Hyperhidrosis:

Hyperhidrosis (2,546 drugs)

Browse all the conditions that are associated with Hyperhidrosis:

Hyperhidrosis (3,546 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on vortioxetine hydrobromide (the active ingredients of Vortioxetine hydrobromide) and Vortioxetine hydrobromide (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.