How effective is Pramipexole Dihydrochloride for Agitation? (a real world drug study)
Summary:
Overall ratings: 3.6/5 Long term ratings: 3.9/5
This is a phase IV clinical study of how effective Pramipexole dihydrochloride (pramipexole dihydrochloride) is for Agitation and for what kind of people. The study is created by eHealthMe from 11 Pramipexole dihydrochloride users and is updated continuously.
What is Pramipexole dihydrochloride?
Pramipexole dihydrochloride has active ingredients of pramipexole dihydrochloride. It is often used in restless leg syndrome. eHealthMe is studying from 5,671 Pramipexole dihydrochloride users. Check the latest studies of Pramipexole dihydrochloride.
What is Agitation?
Agitation (state of anxiety or nervous excitement) is found to be associated with 2,284 drugs and 3,316 conditions by eHealthMe. Check the latest studies of Agitation.
11 people are studied for taking Pramipexole dihydrochloride in Agitation
Overall effectiveness (number of people):
Long term (1+ years) effectiveness (number of people):
Pramipexole dihydrochloride effectiveness for Agitation (number of people):
Overall:
- not at all: 0
- somewhat: 1
- moderate: 4
- high: 4
- very high: 2
Long Term:
- not at all: 0
- somewhat: 0
- moderate: 3
- high: 2
- very high: 2
Gender of people who take Pramipexole dihydrochloride for Agitation *:
- female: 63.64 %
- male: 36.36 %
Age of people who take Pramipexole dihydrochloride for Agitation *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 9.09 %
- 20-29: 9.09 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 36.36 %
- 60+: 45.45 %
Who find Pramipexole Dihydrochloride more effective for Agitation?
Gender of people who take Pramipexole dihydrochloride for Agitation *:
- female: 50 %
- male: 50 %
Age of people who take Pramipexole dihydrochloride for Agitation *:
- 0-1: 0.0 %
- 2-9: 0.0 %
- 10-19: 16.67 %
- 20-29: 0.0 %
- 30-39: 0.0 %
- 40-49: 0.0 %
- 50-59: 33.33 %
- 60+: 50.0 %
* Approximation only. Some reports may have incomplete information.
Do you take Pramipexole dihydrochloride?
- You can start a phase IV clinical trial to monitor Pramipexole dihydrochloride safety and effectiveness.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.
Related publications that referenced our studies:
- Teimoory M, Arefi M, Behnoush B, Bastani B, "Promethazine and Treatment Refractory Agitation in Clonidine Toxicity", International Journal of Medical Toxicology and Forensic Medicine, 2013 Mar .
- Teimoory M, Arefi M, Behnoush B, Bastani B, "Promethazine and Treatment Refractory Agitation in Clonidine Toxicity", International Journal of Medical Toxicology and Forensic Medicine, 2013 Mar .
Related studies
Alternative drugs to, pros and cons of:
- Pramipexole dihydrochloride (5,671 reports)
Treatments, associated drugs and conditions:
- Agitation (142,108 reports)
How the study uses the data?
The study is based on pramipexole dihydrochloride (the active ingredients of Pramipexole dihydrochloride) and Pramipexole dihydrochloride (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 neither.
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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