Flolan and Allopurinol drug interactions - a phase IV clinical study of FDA data

Summary:

Drug interactions are reported among people who take Flolan (epoprostenol sodium) and Allopurinol (allopurinol). Common drug interactions include fluid retention among females and diarrhoea among males.

The phase IV clinical study analyzes what interactions people have when they take Flolan and Allopurinol. It is created by eHealthMe based on reports of 64 people who take the same drugs from the FDA, and is updated regularly.

What is Flolan?

Flolan has active ingredients of epoprostenol sodium. eHealthMe is studying from 10,067 Flolan users. Check the latest studies of Flolan.

What is Allopurinol?

Allopurinol has active ingredients of allopurinol. It is often used in gout. eHealthMe is studying from 190,868 Allopurinol users. Check the latest studies of Allopurinol.



On Jul, 20, 2026

64 people who take Flolan and Allopurinol together, and have interactions are studied.

Flolan and Allopurinol drug interactions.

What are the common drug interactions of Flolan and Allopurinol, by gender? *:

female:

  1. Fluid retention (an abnormal accumulation of fluid in the blood)
  2. Renal impairment (severely reduced kidney function)
  3. Weight increased
  4. Blood iron decreased
  5. Haematocrit decreased
  6. Pulmonary arterial hypertension (high blood pressure in the arteries of lungs)
  7. Sepsis (a severe blood infection that can lead to organ failure and death)
  8. Ascites (accumulation of fluid in the abdominal cavity)
  9. Blood creatinine increased
  10. Disease progression

male:

  1. Diarrhoea
  2. Weight increased
  3. General physical health deterioration (weak health status)
  4. Infusion site erythema (reddening of the skin at infusion site)
  5. Infusion site induration
  6. Infusion site infection
  7. Infusion site inflammation
  8. Infusion site pain
  9. Infusion site swelling
  10. Infusion site warmth

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

0-1:

n/a

2-9:

  1. Ascites (accumulation of fluid in the abdominal cavity)
  2. Sudden death unexplained
  3. Bile duct obstruction (blockage in the tubes that carry bile from the liver to the gallbladder)
  4. Cardiac disorder
  5. Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
  6. Cardiomegaly (increased size of heart than normal)
  7. Chest pain
  8. Pericardial effusion (fluid around the heart)
  9. Right ventricular failure (right half of the heart fails to work)
  10. Tricuspid valve incompetence (inefficient heart valve)

10-19:

  1. Cardiogenic shock (inadequate circulation of blood)
  2. Oliguria (not enough urine)
  3. Pain
  4. Tachycardia (a heart rate that exceeds the range of 100 beats/min)
  5. Aspartate aminotransferase increased
  6. Blood bilirubin increased
  7. Blood lactate dehydrogenase increased
  8. Blood pressure decreased
  9. Hypotension (abnormally low blood pressure)

20-29:

  1. Haematocrit increased
  2. Antinuclear factor positive
  3. Chronic myeloid leukaemia (long lasting type of cancer that starts in the blood-forming cells of the bone marrow and invades the blood)
  4. Colitis ulcerative (inflammation of colon with ulcer)
  5. Drug hypersensitivity
  6. Haematochezia (passage of stools containing blood)
  7. Haemorrhage (bleeding)
  8. Interstitial pneumonia (lung disease characterized by progressive scarring of both lungs)
  9. Leukocytosis (increased white blood cells)
  10. Lung transplant

30-39:

  1. Abscess neck (neck abscesses)
  2. Renal impairment (severely reduced kidney function)
  3. Weight increased
  4. Infusion site erythema (reddening of the skin at infusion site)
  5. Infusion site induration
  6. Infusion site infection
  7. Infusion site inflammation
  8. Infusion site pain
  9. Infusion site swelling
  10. Infusion site warmth

40-49:

  1. Urticaria (rash of round, red welts on the skin that itch intensely)
  2. Oropharyngeal blistering (blister of oropharynx)
  3. Dyspnoea (difficult or laboured respiration)
  4. Oral mucosal blistering (mouth ulcer)
  5. White blood cell count increased
  6. Oedema peripheral (superficial swelling)
  7. Blister (small pocket of fluid within the upper layers of the skin caused by forceful rubbing (friction), burning, freezing, chemical exposure)
  8. Cardiac failure
  9. Diarrhoea
  10. Drug effect decreased

50-59:

  1. Anaemia (lack of blood)
  2. Angioplasty
  3. C-reactive protein increased
  4. Cardiac failure
  5. Death
  6. Electrolyte imbalance
  7. Euphoric mood (excessively happy but may become angry or irritable)
  8. Flushing (the warm, red condition of human skin)
  9. Iatrogenic injury (iatrogenic injury is a form of medical error)
  10. Nasal congestion (blockage of the nasal passages usually due to membranes lining the nose becoming swollen from inflamed blood vessels)

60+:

  1. Fatigue (feeling of tiredness)
  2. Oedema (fluid collection in tissue)
  3. Blood creatinine increased
  4. Disease progression
  5. Haemorrhoids (a swollen vein or group of veins in the region of the anus)
  6. Pulmonary arterial hypertension (high blood pressure in the arteries of lungs)
  7. Renal impairment (severely reduced kidney function)
  8. Right ventricular failure (right half of the heart fails to work)
  9. Sepsis (a severe blood infection that can lead to organ failure and death)
  10. Weight increased

What are the existing conditions these people have? *

  1. Primary Pulmonary Hypertension (primary high blood pressure that affects the arteries in the lungs and the right side of your heart): 39 people, 60.94%
  2. Pulmonary Hypertension (increase in blood pressure in the lung artery): 13 people, 20.31%
  3. Hyperuricaemia (level of uric acid in the blood that is abnormally high): 7 people, 10.94%
  4. Right Ventricular Failure (right half of the heart fails to work): 6 people, 9.38%
  5. Injection Site Pain: 4 people, 6.25%
  6. High Blood Pressure: 4 people, 6.25%

* Approximation only. Some reports may have incomplete information.

Do you take Flolan and Allopurinol?

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Related studies:

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

Browse all drug interactions of Flolan and Allopurinol:

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 Flolan:

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 Allopurinol:

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 Flolan 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 Allopurinol 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 epoprostenol sodium and allopurinol (the active ingredients of Flolan and Allopurinol, respectively), and Flolan and Allopurinol (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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