Soliris and Cfa - a phase IV clinical study of FDA data

Summary:

Cfa is reported as a side effect among people who take Soliris (eculizumab), especially for people who are male, 60+ old, have been taking the drug for < 1 month also take Amlodipine, and have Paroxysmal nocturnal haemoglobinuria.

The phase IV clinical study analyzes which people have Cfa when taking Soliris. It is created by eHealthMe based on reports of 58,774 people who have side effects when taking Soliris from the FDA, and is updated regularly.

What is Soliris?

Soliris has active ingredients of eculizumab. It is often used in paroxysmal nocturnal hemoglobinuria (pnh). eHealthMe is studying from 58,821 Soliris users. Check the latest studies of Soliris.

What is Cfa?

Cfa is found to be associated with 1,977 drugs and 2,268 conditions by eHealthMe. Check the latest studies of Cfa.

On May, 26, 2026

58,774 people reported to have side effects when taking Soliris.
Among them, 16 people (0.03%) have Cfa.

Among these 16 people:

How long have people been on Soliris when they have Cfa? *

What is the gender of people who have Cfa when taking Soliris? *

female: 30 %
male: 70 %

What is the age of people who have Cfa when taking Soliris? *

What are other drugs people take besides Soliris? *

What are other side effects people have besides Cfa? *

Dyspnea (difficult or laboured breathing): 5 people, 31.25%
Cardiac Failure: 5 people, 31.25%
Pleural Effusion (water on the lungs): 4 people, 25.00%
Cardiogenic Shock (inadequate circulation of blood): 4 people, 25.00%
Brain Oedema (excess accumulation of fluid in the intracellular or extracellular spaces of the brain): 3 people, 18.75%
Dyspnea Exertional: 3 people, 18.75%
Fainting (loss of consciousness and postural tone): 3 people, 18.75%
Respiratory Acidosis (respiratory failure or ventilatory failure, causes the ph of blood and other bodily fluids to decrease): 3 people, 18.75%
Renal Impairment (severely reduced kidney function): 3 people, 18.75%
Arrhythmias (irregular heartbeat): 3 people, 18.75%

What are the existing conditions these people have? *

Paroxysmal Nocturnal Haemoglobinuria (haemoglobin in the urine): 8 people, 50.00%
Metabolic Acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body): 2 people, 12.50%
Hypothyroidism (abnormally low activity of the thyroid gland, resulting in retardation of growth and mental development): 2 people, 12.50%
Hyperuricaemia (level of uric acid in the blood that is abnormally high): 2 people, 12.50%
Hyperparathyroidism Secondary (an abnormally high concentration of parathyroid hormone in the blood, resulting in weakening of the bones through loss of calcium-secondary): 2 people, 12.50%
Hyperlipidaemia (presence of excess lipids in the blood): 2 people, 12.50%
High Blood Pressure: 2 people, 12.50%
Haemolytic Uraemic Syndrome (blood clotting disease caused by e. coli infection, birth control pills, pneumonia, medications, and more): 2 people, 12.50%
Thrombotic Microangiopathy (a pathology that results in thrombosis in capillaries and arterioles, due to an endothelial injury): 1 person, 6.25%
Multiple Myeloma (cancer of the plasma cells): 1 person, 6.25%

* Approximation only. Some reports may have incomplete information.

Do you take Soliris and have Cfa?

- Check whether Cfa is associated with a drug or a condition
- Predict drug outcomes for up to one year with AI
- Get an AI agent to monitor your drugs continuously

Related studies:

Effectiveness of, long term effects of, and alternative drugs to Soliris:

Soliris (58,821 reports)

Cfa treatments and more:

Cfa (79,194 reports)

Browse all side effects of Soliris:

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 the drugs that are associated with Cfa:

Cfa (1,977 drugs)

Browse all the conditions that are associated with Cfa:

Cfa (2,268 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on eculizumab (the active ingredients of Soliris) and Soliris (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.