Strattera and Coordination abnormal - a phase IV clinical study of FDA data

Summary:

Coordination abnormal is reported as a side effect among people who take Strattera (atomoxetine hydrochloride), especially for people who are male, 10-19 old, have been taking the drug for 1 - 6 months also take Clonidine, and have Disturbance in attention.

The phase IV clinical study analyzes which people have Coordination abnormal when taking Strattera. It is created by eHealthMe based on reports of 27,428 people who have side effects when taking Strattera from the FDA, and is updated regularly.

What is Strattera?

Strattera has active ingredients of atomoxetine hydrochloride. It is often used in attention deficit hyperactivity disorder. eHealthMe is studying from 29,321 Strattera users. Check the latest studies of Strattera.

What is Coordination abnormal?

Coordination abnormal (abnormal movement) is found to be associated with 1,094 drugs and 1,214 conditions by eHealthMe. Check the latest studies of Coordination abnormal.

On Jan, 12, 2026

27,428 people reported to have side effects when taking Strattera.
Among them, 42 people (0.15%) have Coordination abnormal.

Could Strattera cause Coordination abnormal?

Among these 42 people:

How long have people been on Strattera when they have Coordination abnormal? *

What is the gender of people who have Coordination abnormal when taking Strattera? *

female: 40 %
male: 60 %

What is the age of people who have Coordination abnormal when taking Strattera? *

What are other drugs people take besides Strattera? *

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

Fatigue (feeling of tiredness): 12 people, 28.57%
Hypoaesthesia (reduced sense of touch or sensation): 10 people, 23.81%
Weakness: 10 people, 23.81%
Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body): 9 people, 21.43%
Insomnia (sleeplessness): 9 people, 21.43%
Impulsive Behavior: 9 people, 21.43%
Abnormal Behavior: 8 people, 19.05%
Memory Loss: 8 people, 19.05%
Hypotonia (low muscle tone): 8 people, 19.05%
Confusional State: 8 people, 19.05%

What are the existing conditions these people have? *

Stress And Anxiety: 1 person, 2.38%
Psychomotor Hyperactivity (feelings of extreme restlessness): 1 person, 2.38%
Osteoporosis (bones weak and more likely to break): 1 person, 2.38%
Obsessive-Compulsive Disorder (an anxiety disorder characterized by intrusive thoughts that produce uneasiness, apprehension, fear, or worry;): 1 person, 2.38%
Narcolepsy (brain's inability to regulate sleep-wake cycles normally): 1 person, 2.38%
Muscle Spasticity (tight or stiff muscles and an inability to control those muscles): 1 person, 2.38%
Multiple Sclerosis (a nervous system disease that affects your brain and spinal cord. it damages the myelin sheath): 1 person, 2.38%
Mental Disability: 1 person, 2.38%
High Blood Pressure: 1 person, 2.38%
Disturbance In Attention: 1 person, 2.38%

* Approximation only. Some reports may have incomplete information.

Do you take Strattera and have Coordination abnormal?

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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Strattera:

Strattera (29,321 reports)

Browse all side effects of Strattera:

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 Coordination abnormal:

Coordination abnormal (1,094 drugs)

Browse all the conditions that are associated with Coordination abnormal:

Coordination abnormal (1,214 conditions)

Drugs similar to Strattera and Coordination abnormal :

How the study uses the data?

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