Orenitram and Device dislocation - a phase IV clinical study of FDA data
Summary:
Device dislocation is reported as a side effect among people who take Orenitram (treprostinil), especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months also take Remodulin, and have Primary pulmonary hypertension.
The phase IV clinical study analyzes which people have Device dislocation when taking Orenitram. It is created by eHealthMe based on reports of 17,713 people who have side effects when taking Orenitram from the FDA, and is updated regularly.
What is Orenitram?
Orenitram has active ingredients of treprostinil. eHealthMe is studying from 17,714 Orenitram users. Check the latest studies of Orenitram.
What is Device dislocation?
Device dislocation is found to be associated with 768 drugs and 700 conditions by eHealthMe. Check the latest studies of Device dislocation.
17,713 people reported to have side effects when taking Orenitram.
Among them, 75 people (0.42%) have Device dislocation.
Among these 75 people:
How long have people been on Orenitram when they have Device dislocation? *
What is the gender of people who have Device dislocation when taking Orenitram? *
What is the age of people who have Device dislocation when taking Orenitram? *
What are other drugs people take besides Orenitram? *
What are other side effects people have besides Device dislocation? *
What are the existing conditions these people have? *
* Approximation only. Some reports may have incomplete information.
Do you take Orenitram and have Device dislocation?
- Check whether Device dislocation is associated with a drug or a condition (FREE)
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Related studies:
Effectiveness of, long term effects of, and alternative drugs to Orenitram:
- Orenitram (17,714 reports)
Device dislocation treatments and more:
- Device dislocation (43,936 reports)
How severe was Device dislocation and when was it recovered:
Expand to all the drugs that have ingredients of treprostinil:
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+
Common Orenitram side effects:
- Orenitram side effect: Nausea (feeling of having an urge to vomit) (3,465 reports)
- Orenitram side effect: Fatigue (feeling of tiredness) (1,905 reports)
- Orenitram side effect: Pain in extremity (1,388 reports)
Browse all side effects of Orenitram:
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 zCommon drugs associated with Device dislocation:
- Mirena side effect: Device dislocation (18,167 reports)
- Paragard t 380a side effect: Device dislocation (6,623 reports)
- Nexplanon side effect: Device dislocation (2,609 reports)
- Remodulin side effect: Device dislocation (1,715 reports)
- Implanon side effect: Device dislocation (897 reports)
- Liletta side effect: Device dislocation (781 reports)
- Duopa side effect: Device dislocation (742 reports)
- Opsumit side effect: Device dislocation (739 reports)
- Skyla side effect: Device dislocation (712 reports)
- Aspirin side effect: Device dislocation (674 reports)
Browse all the drugs that are associated with Device dislocation:
- Device dislocation (768 drugs)
Common conditions associated with Device dislocation:
- Family planning and contraception: 24,791 reports
- Parkinsonism: 2,982 reports
- Pulmonary arterial hypertension: 1,912 reports
- Menorrhagia: 1,414 reports
- Rheumatoid arthritis: 735 reports
- Pulmonary hypertension: 520 reports
- Depression: 490 reports
- Pain: 471 reports
- Muscle spasticity: 453 reports
- Hbp: 438 reports
Browse all the conditions that are associated with Device dislocation:
- Device dislocation (700 conditions)
How the study uses the data?
The study uses data from the FDA. It is based on treprostinil (the active ingredients of Orenitram) and Orenitram (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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