Pantoprazole sodium and Atomoxetine hydrochloride drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Pantoprazole sodium (pantoprazole sodium) and Atomoxetine hydrochloride (atomoxetine hydrochloride). Common drug interactions include stomatitis among females and blister among males.
The phase IV clinical study analyzes what interactions people have when they take Pantoprazole sodium and Atomoxetine hydrochloride. It is created by eHealthMe based on reports of 135 people who take the same drugs from the FDA, and is updated regularly.
What is Pantoprazole sodium?
Pantoprazole sodium has active ingredients of pantoprazole sodium. It is often used in gastroesophageal reflux disease. eHealthMe is studying from 66,891 Pantoprazole sodium users. Check the latest studies of Pantoprazole sodium.
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.
135 people who take Pantoprazole sodium and Atomoxetine hydrochloride together, and have interactions are studied.

What are the common drug interactions of Pantoprazole sodium and Atomoxetine hydrochloride, by gender? *
What are the common drug interactions of Pantoprazole sodium and Atomoxetine hydrochloride, by age (0-1 to 60+)? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Pantoprazole sodium and Atomoxetine hydrochloride?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Pantoprazole sodium (66,891 reports)
- Atomoxetine hydrochloride (991 reports)
Browse all drug interactions of Pantoprazole sodium and 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 zSub-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 Pantoprazole sodium:
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 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 zBrowse all interactions between Pantoprazole sodium and drugs from A to Z:
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 interactions between Atomoxetine hydrochloride and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on pantoprazole sodium and atomoxetine hydrochloride (the active ingredients of Pantoprazole sodium and Atomoxetine hydrochloride, respectively), and Pantoprazole sodium and Atomoxetine hydrochloride (the brand names). 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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