Atomoxetine hydrochloride and Pulse abnormal - a phase IV clinical study of FDA data

Summary:

Pulse abnormal is reported as a side effect among people who take Atomoxetine hydrochloride (atomoxetine hydrochloride), especially for people who are female, 40-49 old, also take Synthroid, and have Oral herpes.

The phase IV clinical study analyzes which people have Pulse abnormal when taking Atomoxetine hydrochloride. It is created by eHealthMe based on reports of 971 people who have side effects when taking Atomoxetine hydrochloride from the FDA, and is updated regularly.

What is Atomoxetine hydrochloride?

Atomoxetine hydrochloride has active ingredients of atomoxetine hydrochloride. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 991 Atomoxetine hydrochloride users. Check the latest studies of Atomoxetine hydrochloride.

What is Pulse abnormal?

Pulse abnormal is found to be associated with 437 drugs and 489 conditions by eHealthMe. Check the latest studies of Pulse abnormal.

On Jul, 20, 2026

971 people reported to have side effects when taking Atomoxetine hydrochloride.
Among them, 31 people (3.19%) have Pulse abnormal.

Could Atomoxetine hydrochloride cause Pulse abnormal?

Among these 31 people:

What is the gender of people who have Pulse abnormal when taking Atomoxetine hydrochloride? *

female: 100 %
male: 0.0 %

What is the age of people who have Pulse abnormal when taking Atomoxetine hydrochloride? *

What are other drugs people take besides Atomoxetine hydrochloride? *

Amlodipine Besylate: 31 people, 100.00%
Tylenol: 31 people, 100.00%
Synthroid: 31 people, 100.00%
Vyvanse: 29 people, 93.55%
Clonidine: 29 people, 93.55%
Risperidone: 28 people, 90.32%
Dexmethylphenidate Hydrochloride: 28 people, 90.32%
Quetiapine Fumarate: 27 people, 87.10%
Venlafaxine Hydrochloride: 26 people, 83.87%
Methylphenidate Hydrochloride: 25 people, 80.65%

What are other side effects people have besides Pulse abnormal? *

Withdrawal Syndrome (a discontinuation syndrome is a set of symptoms occurred due to discontinuation of substance): 31 people, 100.00%
Wheezing (a high-pitched whistling sound made while you breath): 31 people, 100.00%
Appetite - Decreased (decreased appetite occurs when you have a reduced desire to eat): 31 people, 100.00%
Confusional State: 31 people, 100.00%
Cough: 31 people, 100.00%
Disturbance In Attention: 31 people, 100.00%
Dizziness: 31 people, 100.00%
Drowsiness: 31 people, 100.00%
Dyspnea (difficult or laboured breathing): 31 people, 100.00%
Fatigue (feeling of tiredness): 31 people, 100.00%

What are the existing conditions these people have? *

Oral Herpes (viral infection of mouth): 29 people, 93.55%
High Blood Pressure: 28 people, 90.32%

* Approximation only. Some reports may have incomplete information.

Do you take Atomoxetine hydrochloride and have Pulse abnormal?

- Check whether Pulse abnormal 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 Atomoxetine hydrochloride:

Atomoxetine hydrochloride (991 reports)

Pulse abnormal treatments and more:

Pulse abnormal (2,933 reports)

Browse all side effects of Atomoxetine hydrochloride:

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 Pulse abnormal:

Pulse abnormal (437 drugs)

Browse all the conditions that are associated with Pulse abnormal:

Pulse abnormal (489 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on atomoxetine hydrochloride (the active ingredients of Atomoxetine hydrochloride) and Atomoxetine hydrochloride (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.