Actigall and Amaryl drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Actigall (ursodiol) and Amaryl (glimepiride). Common drug interactions include blood bilirubin increased among females and anastomotic stenosis among males.
The phase IV clinical study analyzes what interactions people have when they take Actigall and Amaryl. It is created by eHealthMe based on reports of 17 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 Amaryl?
Amaryl has active ingredients of glimepiride. It is often used in diabetes. eHealthMe is studying from 32,259 Amaryl users. Check the latest studies of Amaryl.
17 people who take Actigall and Amaryl together, and have interactions are studied.

What are the common drug interactions of Actigall and Amaryl, by gender? *:
female:
- Blood bilirubin increased
- Erythema (redness of the skin)
- Fall
- Foot ulcer
- Hepatitis a antibody positive
- Leg ulcer (exc varicose) (leg ulcer without varicose vein)
- Markedly reduced food intake
- Pain in limb
- Pyrexia (fever)
- Septicaemia escherichial (bacterial blood infection)
male:
- Anastomotic stenosis
- Cholangitis (infection of the bile duct)
- Erythema (redness of the skin)
- Fibrosis (formation of excess fibrous connective tissue in an organ or tissue)
- Gait disturbance
- General physical health deterioration (weak health status)
- Hepatic artery occlusion (the blockage in hepatic artery)
- Hyperkeratosis (thickening of the outer layer of the skin)
- Hypoaesthesia (reduced sense of touch or sensation)
- Joint contracture (a permanent shortening of a muscle or joint)
What are the common drug interactions of Actigall and Amaryl, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
n/a
50-59:
- Post procedural complication
- Pulmonary embolism (blockage of the main artery of the lung)
- Pulmonary mass
- Pyrexia (fever)
- Secondary adrenocortical insufficiency (inadequate secretion of acth by the pituitary gland)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Septicaemia escherichial (bacterial blood infection)
- Skin discolouration (change of skin colour)
- Thrombocytopenia (decrease of platelets in blood)
- Urinary tract infection enterococcal
60+:
- Abscess jaw (tooth abscess or root abscess)
- Arteriosclerosis (thickening and hardening of arteries)
- Excessive granulation tissue (excessive collagen-rich tissue which forms at the site of an injury)
- Eye pruritus (eye itching)
- Fatigue (feeling of tiredness)
- Fistula (an abnormal connection or passageway between two)
- Gynaecomastia (enlargement of the gland tissue of the male breast)
- Hypoglycaemia (deficiency of glucose in the bloodstream)
- Hypogonadism male (male testes produce little or no sex hormone)
- Impaired healing
What are the existing conditions these people have? *
- Liver Transplant Rejection (failure of liver transplant): 4 people, 23.53%
- Nuclear Magnetic Resonance Imaging Brain: 3 people, 17.65%
- Pyogenic Liver Abscess (liver abscess caused by bacteria): 2 people, 11.76%
- Urinary Tract Infection: 1 person, 5.88%
- High Blood Pressure: 1 person, 5.88%
- Graft Versus Host Disease (the donated bone marrow or stem cells view the recipient's body as foreign, and the donated cells/bone marrow attack the body): 1 person, 5.88%
- Depression: 1 person, 5.88%
- Deep Venous Thrombosis (blood clot in a major vein that usually develops in the legs and/or pelvis): 1 person, 5.88%
- Constipation: 1 person, 5.88%
- Chronic Graft Versus Host Disease (immune cells attack the host's body cells after transplant): 1 person, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Actigall and Amaryl?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Actigall and Amaryl:
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 Amaryl:
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 Amaryl 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 glimepiride (the active ingredients of Actigall and Amaryl, respectively), and Actigall and Amaryl (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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