Actigall and Duragesic drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Actigall (ursodiol) and Duragesic (fentanyl). Common drug interactions include nausea among females and arthralgia among males.
The phase IV clinical study analyzes what interactions people have when they take Actigall and Duragesic. It is created by eHealthMe based on reports of 27 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 Duragesic?
Duragesic has active ingredients of fentanyl. eHealthMe is studying from 66,597 Duragesic users. Check the latest studies of Duragesic.
27 people who take Actigall and Duragesic together, and have interactions are studied.

What are the common drug interactions of Actigall and Duragesic, by gender? *:
female:
- Nausea (feeling of having an urge to vomit)
- Arterial occlusive disease (slow process through which arteries throughout the body become progressively narrowed and eventually completely blocked)
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Fatigue (feeling of tiredness)
- Hot flush (sudden feelings of heat)
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Withdrawal syndrome (a discontinuation syndrome is a set of symptoms occurred due to discontinuation of substance)
- Gastrooesophageal reflux disease (stomach contents (food or liquid) leak backwards from the stomach into the oesophagus)
- Asthenia (weakness)
male:
- Arthralgia (joint pain)
- Deformity (disfigurement)
- Joint range of motion decreased (disease of joint movement)
- Mobility decreased (ability to move is reduced)
- Musculoskeletal stiffness (stiffness of the body's muscles, joints, tendons, ligaments and nerves)
- Nephrogenic systemic fibrosis (involves fibrosis of skin, joints, eyes due to kidney disease)
- Oedema (fluid collection in tissue)
- Oedema peripheral (superficial swelling)
- Pain
- Pain in extremity
What are the common drug interactions of Actigall and Duragesic, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Hepatic failure (liver failure)
30-39:
n/a
40-49:
- Abdominal pain
- Application site irritation
- Application site reaction
- Blister (small pocket of fluid within the upper layers of the skin caused by forceful rubbing (friction), burning, freezing, chemical exposure)
- Crohn's disease (a condition that causes inflammation of the gastrointestinal tract)
- Dehydration (dryness resulting from the removal of water)
- Drug withdrawal syndrome (interfere with normal social, occupational, or other functioning. are not due to another medical condition, drug use, or discontinuation)
- Erythema (redness of the skin)
- Haemorrhage (bleeding)
- Intestinal obstruction
50-59:
- Arthralgia (joint pain)
- Deformity (disfigurement)
- 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)
- 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)
- Joint range of motion decreased (disease of joint movement)
60+:
- Nausea (feeling of having an urge to vomit)
- Arterial occlusive disease (slow process through which arteries throughout the body become progressively narrowed and eventually completely blocked)
- Death
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Ascites (accumulation of fluid in the abdominal cavity)
- Asthenia (weakness)
- Chronic hepatic failure (long lasting liver failure)
- Confusional state
- Constipation
- Decreased appetite
What are the existing conditions these people have? *
- Pain: 10 people, 37.04%
- Back Pain: 7 people, 25.93%
- Hepatic Steatosis (fatty liver disease): 5 people, 18.52%
- Gastric Disorder (disease of stomach): 5 people, 18.52%
- Cholangiocarcinoma (a cancer that forms glands or secretes significant amounts of mucins): 5 people, 18.52%
- Nuclear Magnetic Resonance Imaging Brain: 3 people, 11.11%
- Cough: 3 people, 11.11%
- Nausea (feeling of having an urge to vomit): 2 people, 7.41%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 2 people, 7.41%
- Gallbladder Disorder: 2 people, 7.41%
* Approximation only. Some reports may have incomplete information.
Do you take Actigall and Duragesic?
- 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 Duragesic:
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 Duragesic:
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 Duragesic 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 fentanyl (the active ingredients of Actigall and Duragesic, respectively), and Actigall and Duragesic (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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