Ampyra and Dysgraphia - a phase IV clinical study of FDA data
Summary:
Dysgraphia is reported as a side effect among people who take Ampyra (dalfampridine), especially for people who are female, 60+ old, have been taking the drug for 2 - 5 years also take Tysabri, and have Gait disturbance.
The phase IV clinical study analyzes which people have Dysgraphia when taking Ampyra. It is created by eHealthMe based on reports of 76,998 people who have side effects when taking Ampyra from the FDA, and is updated regularly.
What is Ampyra?
Ampyra has active ingredients of dalfampridine. It is often used in multiple sclerosis. eHealthMe is studying from 77,145 Ampyra users. Check the latest studies of Ampyra.
What is Dysgraphia?
Dysgraphia (impaired ability to learn to write) is found to be associated with 554 drugs and 652 conditions by eHealthMe. Check the latest studies of Dysgraphia.
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 >>>.
76,998 people reported to have side effects when taking Ampyra.
Among them, 372 people (0.48%) have Dysgraphia.

Among these 372 people:
How long have people been on Ampyra when they have Dysgraphia? *
What is the gender of people who have Dysgraphia when taking Ampyra? *
What is the age of people who have Dysgraphia when taking Ampyra? *
What are other drugs people take besides Ampyra? *
What are other side effects people have besides Dysgraphia? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Ampyra and have Dysgraphia?
- Check whether Dysgraphia 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 Ampyra:
- Ampyra (77,145 reports)
Dysgraphia treatments and more:
- Dysgraphia (7,998 reports)
How severe was Dysgraphia and when was it recovered:
Expand to all the drugs that have ingredients of dalfampridine:
- Dysgraphia and drugs with ingredients of dalfampridine (375 reports)
Sub-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 Ampyra:
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 the drugs that are associated with Dysgraphia:
- Dysgraphia (554 drugs)
Browse all the conditions that are associated with Dysgraphia:
- Dysgraphia (652 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on dalfampridine (the active ingredients of Ampyra) and Ampyra (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.
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