Remodulin and Apixaban drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Remodulin (treprostinil sodium) and Apixaban (apixaban). Common drug interactions include general physical health deterioration among females and septic shock among males.

The phase IV clinical study analyzes what interactions people have when they take Remodulin and Apixaban. It is created by eHealthMe based on reports of 52 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 Apixaban?

Apixaban has active ingredients of apixaban. It is often used in blood clots. eHealthMe is studying from 60,349 Apixaban users. Check the latest studies of Apixaban.



On Jul, 05, 2026

52 people who take Remodulin and Apixaban together, and have interactions are studied.

Remodulin and Apixaban drug interactions.

What are the common drug interactions of Remodulin and Apixaban, by gender? *:

female:

  1. General physical health deterioration (weak health status)
  2. Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
  3. Uterine haemorrhage (uterine bleeding)
  4. Pulmonary hypertension (increase in blood pressure in the lung artery)
  5. Burning sensation
  6. Chest pain
  7. Dizziness
  8. Erythema (redness of the skin)
  9. Fatigue (feeling of tiredness)
  10. Heart rate increased

male:

  1. Septic shock (shock due to blood infection)
  2. Cardiac failure
  3. Back pain
  4. Fluid retention (an abnormal accumulation of fluid in the blood)
  5. Injection site erythema (redness at injection site)
  6. Weight decreased
  7. Hypotension (abnormally low blood pressure)
  8. Abdominal discomfort
  9. Cough
  10. Device occlusion

What are the common drug interactions of Remodulin and Apixaban, by age (0-1 to 60+)? *:

0-1:

n/a

2-9:

n/a

10-19:

  1. Uterine haemorrhage (uterine bleeding)
  2. Hyperthyroidism (over activity of the thyroid gland)
  3. Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development)
  4. Thrombocytopenia (decrease of platelets in blood)
  5. Weight decreased
  6. General physical health deterioration (weak health status)
  7. Headache (pain in head)
  8. Hypoxia (low oxygen in tissues)
  9. Nausea (feeling of having an urge to vomit)
  10. Rhinovirus infection

20-29:

  1. Fatigue (feeling of tiredness)
  2. Headache (pain in head)
  3. Hospitalisation
  4. Nausea (feeling of having an urge to vomit)

30-39:

  1. Dyspnoea (difficult or laboured respiration)
  2. Hospitalisation
  3. Nausea (feeling of having an urge to vomit)
  4. Ascites (accumulation of fluid in the abdominal cavity)
  5. Blood pressure decreased
  6. Body temperature increased
  7. Cardiac disorder
  8. Cardiac failure
  9. Death
  10. Headache (pain in head)

40-49:

  1. Septic shock (shock due to blood infection)
  2. Back pain
  3. Blood creatinine increased
  4. Diarrhoea
  5. Fluid overload (too much fluid in the blood)
  6. Fluid retention (an abnormal accumulation of fluid in the blood)
  7. Oedema peripheral (superficial swelling)
  8. Oliguria (not enough urine)
  9. Renal failure (kidney dysfunction)
  10. Renal impairment (severely reduced kidney function)

50-59:

  1. Peripheral swelling
  2. Pneumonia
  3. Respiratory failure (inadequate gas exchange by the respiratory system)
  4. Injection site discharge
  5. Injection site exfoliation (removal of the oldest dead skin from injection site)
  6. Injection site hypersensitivity
  7. Injection site irritation
  8. Abdominal discomfort
  9. Abdominal pain
  10. Anaemia (lack of blood)

60+:

  1. Fluid retention (an abnormal accumulation of fluid in the blood)
  2. Dyspnoea (difficult or laboured respiration)
  3. Burning sensation
  4. Haemoptysis (blood-stained sputum from the bronchi, larynx, trachea, or lungs)
  5. Chest pain
  6. Death
  7. Dizziness
  8. Abdominal discomfort
  9. Heart rate increased
  10. Hospitalisation

What are the existing conditions these people have? *

  1. Pulmonary Hypertension (increase in blood pressure in the lung artery): 12 people, 23.08%
  2. Wheezing (a high-pitched whistling sound made while you breath): 4 people, 7.69%
  3. Migraine (headache): 4 people, 7.69%
  4. Anaphylaxis (serious allergic reaction that is rapid in onset and may cause death): 4 people, 7.69%
  5. Pulmonary Thrombosis (scarring in the lungs): 3 people, 5.77%
  6. Pain: 3 people, 5.77%
  7. Nausea And Vomiting: 3 people, 5.77%
  8. Nausea (feeling of having an urge to vomit): 3 people, 5.77%
  9. Headache (pain in head): 3 people, 5.77%
  10. Fever: 3 people, 5.77%

* Approximation only. Some reports may have incomplete information.

Do you take Remodulin and Apixaban?

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Related studies:

Effectiveness of, side effects of, and alternative drugs to the 2 drugs:

Browse all drug interactions of Remodulin and Apixaban:

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 z

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 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 z

Browse all side effects of Apixaban:

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 z

Browse 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 z

Browse all interactions between Apixaban 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 z

How the study uses the data?

The study uses data from the FDA. It is based on treprostinil sodium and apixaban (the active ingredients of Remodulin and Apixaban, respectively), and Remodulin and Apixaban (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.

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