Dysport and Oedema aggravated - a phase IV clinical study of FDA data
Summary:
Oedema aggravated is reported as a side effect among people who take Dysport (abobotulinumtoxina), especially for people who are female, 40-49 old, have been taking the drug for < 1 month also take Baclofen, and have Skin wrinkling.
The phase IV clinical study analyzes which people have Oedema aggravated when taking Dysport. It is created by eHealthMe based on reports of 6,319 people who have side effects when taking Dysport from the FDA, and is updated regularly.
What is Dysport?
Dysport has active ingredients of abobotulinumtoxina. It is often used in wrinkles. eHealthMe is studying from 6,349 Dysport users. Check the latest studies of Dysport.
What is Oedema aggravated?
Oedema aggravated (fluid collection in tissue) is found to be associated with 1,606 drugs and 583 conditions by eHealthMe. Check the latest studies of Oedema aggravated.
6,319 people reported to have side effects when taking Dysport.
Among them, 16 people (0.25%) have Oedema aggravated.

Among these 16 people:
How long have people been on Dysport when they have Oedema aggravated? *
- < 1 month: 100 %
- 1 - 6 months: 0.0 %
- 6 - 12 months: 0.0 %
- 1 - 2 years: 0.0 %
- 2 - 5 years: 0.0 %
- 5 - 10 years: 0.0 %
- 10+ years: 0.0 %
What is the gender of people who have Oedema aggravated when taking Dysport? *
- female: 63.64 %
- male: 36.36 %
What is the age of people who have Oedema aggravated when taking Dysport? *
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 0.0 %
- 20-29: 0.0 %
- 30-39: 33.33 %
- 40-49: 50.0 %
- 50-59: 0.0 %
- 60+: 16.67 %
What are other drugs people take besides Dysport? *
- Medrol: 1 person, 6.25%
- Baclofen: 1 person, 6.25%
What are other side effects people have besides Oedema aggravated? *
- Hypersensitivity: 4 people, 25.00%
- Injection Site Pain: 4 people, 25.00%
- Rashes (redness): 3 people, 18.75%
- Weakness: 2 people, 12.50%
- Drug Ineffective: 2 people, 12.50%
- Eyelid Ptosis (falling of the upper or lower eyelid): 2 people, 12.50%
- Hyperaemia (increase of blood flow to different tissues in the body): 2 people, 12.50%
- Localised Oedema (fluid retention in a particular part of the body): 1 person, 6.25%
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body): 1 person, 6.25%
- Eye Discharge: 1 person, 6.25%
What are the existing conditions these people have? *
- Skin Wrinkling (wrinkle on skin): 8 people, 50.00%
- Hypertonia (abnormal increase in muscle tension and a reduced ability of a muscle to stretch): 2 people, 12.50%
- Torticollis (a twisted neck in which the head is tipped to one side, while the chin is turned to the other): 1 person, 6.25%
- Muscle Spasticity (tight or stiff muscles and an inability to control those muscles): 1 person, 6.25%
- Hypersensitivity: 1 person, 6.25%
* Approximation only. Some reports may have incomplete information.
Do you take Dysport and have Oedema aggravated?
- Check whether Oedema aggravated 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 Dysport:
- Dysport (6,349 reports)
Oedema aggravated treatments and more:
- Oedema aggravated (37 reports)
How severe was Oedema aggravated and when was it recovered:
Expand to all the drugs that have ingredients of abobotulinumtoxina:
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 Dysport:
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 Oedema aggravated:
- Oedema aggravated (1,606 drugs)
Browse all the conditions that are associated with Oedema aggravated:
- Oedema aggravated (583 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on abobotulinumtoxina (the active ingredients of Dysport) and Dysport (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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