Remodulin and Pentoxifylline drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Remodulin (treprostinil sodium) and Pentoxifylline (pentoxifylline). Common drug interactions include hypersensitivity among females and device failure among males.
The phase IV clinical study analyzes what interactions people have when they take Remodulin and Pentoxifylline. It is created by eHealthMe based on reports of 14 people who take the same drugs from the FDA, and is updated regularly.
What is Remodulin?
Remodulin has active ingredients of treprostinil sodium. It is often used in primary pulmonary hypertension. eHealthMe is studying from 55,843 Remodulin users. Check the latest studies of Remodulin.
What is Pentoxifylline?
Pentoxifylline has active ingredients of pentoxifylline. eHealthMe is studying from 5,997 Pentoxifylline users. Check the latest studies of Pentoxifylline.
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 >>>.
14 people who take Remodulin and Pentoxifylline together, and have interactions are studied.

What are the common drug interactions of Remodulin and Pentoxifylline, by gender? *:
female:
- Hypersensitivity
- Immune system disorder
- Secretion discharge
- Sinusitis (inflammation of sinus)
- Vomiting
- Breast swelling
- Cerebral haemorrhage (bleeding within the brain)
- Fall
- Head injury
- Loss of consciousness
male:
- Device failure
- Scleroderma (hard skin)
- Encephalopathy (functioning of the brain is affected by some agent or condition)
- Malignant atrophic papulosis (an extremely rare vascular weakness that affects the lining of the medium and small veins and arteries)
- Nervous system disorder (a general class of medical conditions affecting the nervous system)
What are the common drug interactions of Remodulin and Pentoxifylline, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Encephalopathy (functioning of the brain is affected by some agent or condition)
- Malignant atrophic papulosis (an extremely rare vascular weakness that affects the lining of the medium and small veins and arteries)
- Nervous system disorder (a general class of medical conditions affecting the nervous system)
20-29:
n/a
30-39:
- Catheter related infection
- Stenotrophomonas sepsis (blood infection by stenotrophomonas)
40-49:
n/a
50-59:
- Influenza
- Weight decreased
- Pneumonia
- Cerebral haemorrhage (bleeding within the brain)
- Fall
- Head injury
- Loss of consciousness
- Pain
- Hypervolaemia (abnormally increased volume of blood)
60+:
- Device failure
- Scleroderma (hard skin)
- Peripheral swelling
- Pneumonia
- Respiratory distress (difficulty in breathing)
- Secretion discharge
- Vomiting
- Chills (felling of cold)
- Dizziness
- Dyspnoea (difficult or laboured respiration)
What are the existing conditions these people have? *
- Pulmonary Hypertension (increase in blood pressure in the lung artery): 1 person, 7.14%
- Portopulmonary Hypertension (coexistence of portal and pulmonary hypertension): 1 person, 7.14%
- Malignant Atrophic Papulosis (an extremely rare vascular weakness that affects the lining of the medium and small veins and arteries): 1 person, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Remodulin and Pentoxifylline?
- Personalize this study to your gender, age, symptoms and drugs
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously
Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
- Remodulin (55,843 reports)
- Pentoxifylline (5,997 reports)
Browse all drug interactions of Remodulin and Pentoxifylline:
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 zSub-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 Remodulin:
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 side effects of Pentoxifylline:
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 interactions between Remodulin and drugs from A to Z:
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 interactions between Pentoxifylline and drugs from A to Z:
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 zHow the study uses the data?
The study uses data from the FDA. It is based on treprostinil sodium and pentoxifylline (the active ingredients of Remodulin and Pentoxifylline, respectively), and Remodulin and Pentoxifylline (the brand names). 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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