Actigall and Soliris drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Actigall (ursodiol) and Soliris (eculizumab). Common drug interactions include drug ineffective among females.
The phase IV clinical study analyzes what interactions people have when they take Actigall and Soliris. 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 Actigall?
Actigall has active ingredients of ursodiol. It is often used in gallstones. eHealthMe is studying from 2,162 Actigall users. Check the latest studies of Actigall.
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.
14 people who take Actigall and Soliris together, and have interactions are studied.

What are the common drug interactions of Actigall and Soliris, by gender? *:
female:
- Drug ineffective
- Renal failure acute (rapid kidney dysfunction)
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Post procedural haemorrhage (post procedural bleeding)
- Splenomegaly (enlargement of spleen)
- Staphylococcal infection (an infection with staphylococcus bacteria)
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
- Acute myocardial infarction (acute heart attack)
- Asthenia (weakness)
- Blood lactate dehydrogenase increased
male:
n/a
What are the common drug interactions of Actigall and Soliris, by age (0-1 to 60+)? *:
0-1:
- Erythema multiforme (a type of hypersensitivity reaction)
2-9:
n/a
10-19:
n/a
20-29:
- Gastrointestinal fungal infection
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
- Intestinal ulcer
- Oral fungal infection
- Rectal haemorrhage (bleeding from anus)
30-39:
- Blood creatinine increased
- Blood lactate dehydrogenase increased
- Haemolysis (breaking open of red blood cells and the release of haemoglobin into the surrounding fluid)
- Hepatic enzyme increased
- Nausea (feeling of having an urge to vomit)
- Abdominal pain upper
- Acute respiratory distress syndrome
- Disorientation (disability in which the senses of time, direction, and recognition of people and places)
- Dizziness
- Gastroenteritis viral (inflammation of stomach and intestine caused by virus infection)
40-49:
n/a
50-59:
n/a
60+:
- Drug ineffective
- Abscess (pus)
- Renal failure acute (rapid kidney dysfunction)
- Splenomegaly (enlargement of spleen)
- Staphylococcal infection (an infection with staphylococcus bacteria)
- Acute myocardial infarction (acute heart attack)
- Asthenia (weakness)
- Cachexia (loss of weight)
- Depression
- Fall
What are the existing conditions these people have? *
- Paroxysmal Nocturnal Haemoglobinuria (haemoglobin in the urine): 11 people, 78.57%
- Liver Disorder (liver diseases): 3 people, 21.43%
- Heart Rate Increased: 3 people, 21.43%
- Haemolytic Uraemic Syndrome (blood clotting disease caused by e. coli infection, birth control pills, pneumonia, medications, and more): 2 people, 14.29%
- Urinary Tract Infection: 1 person, 7.14%
- Pain: 1 person, 7.14%
- Nausea (feeling of having an urge to vomit): 1 person, 7.14%
- Myelodysplastic Syndrome (a group of conditions that occur when the blood-forming cells in the bone marrow are damaged): 1 person, 7.14%
- Insomnia (sleeplessness): 1 person, 7.14%
- High Blood Pressure: 1 person, 7.14%
* Approximation only. Some reports may have incomplete information.
Do you take Actigall and Soliris?
- 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:
Browse all drug interactions of Actigall and 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 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 Actigall:
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 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 zBrowse all interactions between Actigall 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 Soliris 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 ursodiol and eculizumab (the active ingredients of Actigall and Soliris, respectively), and Actigall and Soliris (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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