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

Summary:

Drug interactions are reported among people who take Cozaar (losartan potassium) and Remodulin (treprostinil sodium). Common drug interactions include cardiac failure acute among females and fatigue among males.

The phase IV clinical study analyzes what interactions people have when they take Cozaar and Remodulin. It is created by eHealthMe based on reports of 48 people who take the same drugs from the FDA, and is updated regularly.

What is Cozaar?

Cozaar has active ingredients of losartan potassium. It is often used in high blood pressure. eHealthMe is studying from 45,124 Cozaar users. Check the latest studies of Cozaar.

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.



On Aug, 09, 2026

48 people who take Cozaar and Remodulin together, and have interactions are studied.

Cozaar and Remodulin drug interactions.

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

female:

  1. Cardiac failure acute
  2. Catheter site erythema (redness of skin at catheter site)
  3. Catheter site pain
  4. Dysphagia (a condition in which swallowing is difficult or painful)
  5. Epistaxis (bleed from the nose)
  6. Flushing (the warm, red condition of human skin)
  7. Heart rate increased
  8. Hypoacusis (loss of hearing)
  9. Hypokalaemia (low potassium)
  10. Hypomagnesaemia (electrolyte disturbance in which there is an abnormally low level of magnesium in the blood)

male:

  1. Fatigue (feeling of tiredness)
  2. Headache (pain in head)
  3. Infusion site pain
  4. Pleural effusion (water on the lungs)
  5. Ascites (accumulation of fluid in the abdominal cavity)
  6. Cardiac arrest
  7. Cardiomegaly (increased size of heart than normal)
  8. Convulsions (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled of muscles contract and relax rapidly and repeatedly)
  9. Disseminated intravascular coagulation (systemic activation of blood coagulation)
  10. Dizziness

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

0-1:

n/a

2-9:

n/a

10-19:

n/a

20-29:

n/a

30-39:

  1. Chest pain
  2. Dyspnoea (difficult or laboured respiration)
  3. Dizziness
  4. Oedema peripheral (superficial swelling)
  5. Ascites (accumulation of fluid in the abdominal cavity)
  6. Cardiac arrest
  7. Cardiomegaly (increased size of heart than normal)
  8. Convulsions (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled of muscles contract and relax rapidly and repeatedly)
  9. Disseminated intravascular coagulation (systemic activation of blood coagulation)
  10. Grunting (abnormal, short, deep, hoarse sounds in exhalation that often accompany severe chest pain)

40-49:

  1. Headache (pain in head)
  2. Infusion site pain
  3. Limb discomfort (discomfort in leg)
  4. Nausea (feeling of having an urge to vomit)
  5. Peripheral swelling
  6. Pneumonia
  7. Pruritus (severe itching of the skin)
  8. Rash
  9. Skin discolouration (change of skin colour)
  10. Sluggishness (lacking alertness)

50-59:

  1. Bradycardia (abnormally slow heart action)
  2. Dizziness postural
  3. Fatigue (feeling of tiredness)
  4. Flushing (the warm, red condition of human skin)
  5. Headache (pain in head)
  6. Hypotension (abnormally low blood pressure)
  7. Infusion site pain
  8. Malaise (a feeling of general discomfort or uneasiness)
  9. Nausea (feeling of having an urge to vomit)
  10. Syncope (loss of consciousness with an inability to maintain postural tone)

60+:

  1. Fatigue (feeling of tiredness)
  2. Headache (pain in head)
  3. Nausea (feeling of having an urge to vomit)
  4. Influenza
  5. Anaemia (lack of blood)
  6. Catheter site erythema (redness of skin at catheter site)
  7. Death
  8. Vomiting
  9. Dizziness
  10. Fluid retention (an abnormal accumulation of fluid in the blood)

What are the existing conditions these people have? *

  1. Pulmonary Hypertension (increase in blood pressure in the lung artery): 10 people, 20.83%
  2. High Blood Cholesterol: 4 people, 8.33%
  3. Systemic Sclerosis (Scleroderma) (an autoimmune or connective tissue disease. it is characterized by thickening of the skin): 3 people, 6.25%
  4. Nausea (feeling of having an urge to vomit): 3 people, 6.25%
  5. Diarrhea: 3 people, 6.25%

* Approximation only. Some reports may have incomplete information.

Do you take Cozaar and Remodulin?

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Related studies:

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

Browse all drug interactions of Cozaar and 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

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 Cozaar:

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 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 interactions between Cozaar 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 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

Related publications that referenced our studies


How the study uses the data?

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