Antara and Digoxin drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Antara (fenofibrate) and Digoxin (digoxin). Common drug interactions include oedema among females and dyspnoea among males.
The phase IV clinical study analyzes what interactions people have when they take Antara and Digoxin. 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 Antara?
Antara has active ingredients of fenofibrate. It is often used in high blood cholesterol. eHealthMe is studying from 569 Antara users. Check the latest studies of Antara.
What is Digoxin?
Digoxin has active ingredients of digoxin. It is often used in atrial fibrillation/flutter. eHealthMe is studying from 93,740 Digoxin users. Check the latest studies of Digoxin.
27 people who take Antara and Digoxin together, and have interactions are studied.

What are the common drug interactions of Antara and Digoxin, by gender? *:
female:
- Oedema (fluid collection in tissue)
- Retinal haemorrhage (bleeding from retina)
- Tremor (trembling or shaking movements in one or more parts of your body)
- Urinary tract infection
- Abdominal pain lower
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Hypoaesthesia (reduced sense of touch or sensation)
- Injury
- Myalgia (muscle pain)
- Neuropathy peripheral (surface nerve damage)
male:
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Back pain
- Cellulitis (infection under the skin)
- Chest discomfort
- Chest pain
- Chills (felling of cold)
- Chronic kidney disease
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
- Coronary artery disease (plaque building up along the inner walls of the arteries of the heart, which narrows the arteries and restricts blood flow to the heart)
What are the common drug interactions of Antara and Digoxin, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Coagulopathy (blood's ability to clot is impaired)
- Mydriasis (a dilation of the pupil)
- Osteoporotic fracture (fracture due to weak bone)
- Peptic ulcer
- Retinopathy (acute damage to the retina of the eye)
- Upper gastrointestinal haemorrhage (upper gastrointestinal bleeding)
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Asthenia (weakness)
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Bundle branch block left (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the left ventricle)
- Cardiac disorder
- Cardiac failure chronic
- Cardiac valve disease (heart valve disease)
- Cardiomyopathy (weakening of the heart muscle)
- Cellulitis (infection under the skin)
- Chest pain
- Conduction disorder (serious disorder of the heart not responses proper to impulses)
50-59:
- Anxiety
- Dyspnoea (difficult or laboured respiration)
- Fatigue (feeling of tiredness)
- Oedema peripheral (superficial swelling)
- Tachycardia (a heart rate that exceeds the range of 100 beats/min)
60+:
- Nausea (feeling of having an urge to vomit)
- Coronary artery occlusion (complete obstruction of blood flow in a coronary artery)
- Hypertension (high blood pressure)
- Adnexa uteri cyst (ovarian cysts)
- Hyperkalaemia (damage to or disease of the kidney)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Nephropathy (damage to or disease of a kidney)
- Polydipsia (excessive thirst)
- Anxiety
- Cardiac failure congestive
What are the existing conditions these people have? *
- Arrhythmias (irregular heartbeat): 8 people, 29.63%
- High Blood Pressure: 5 people, 18.52%
- Cardiac Disorder: 4 people, 14.81%
- Infection: 3 people, 11.11%
- Pain: 3 people, 11.11%
- Diabetes: 3 people, 11.11%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 11.11%
- Hypersensitivity: 2 people, 7.41%
- Bladder Disorder: 2 people, 7.41%
- Headache (pain in head): 2 people, 7.41%
* Approximation only. Some reports may have incomplete information.
Do you take Antara and Digoxin?
- 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 Antara and Digoxin:
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 Antara:
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 Digoxin:
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 Antara 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 Digoxin 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 zRelated publications that referenced our studies
- Guru SR, Suresh A, Padmanabhan S, Reddy A, "A Rare Case of Digoxin Associated Gingival Overgrowth", Journal of clinical and diagnostic research: JCDR, 2017 Jan .
- Lai SW, Lin CL, Liao KF, "Digoxin use may increase the relative risk of acute pancreatitis: a population-based case–control study in Taiwan", International journal of cardiology, 2015 Feb .
- Guru SR, Suresh A, Padmanabhan S, Reddy A, "A Rare Case of Digoxin Associated Gingival Overgrowth", Journal of clinical and diagnostic research: JCDR, 2017 Jan .
- Lai SW, Lin CL, Liao KF, "Digoxin use may increase the relative risk of acute pancreatitis: a population-based case–control study in Taiwan", International journal of cardiology, 2015 Feb .
How the study uses the data?
The study uses data from the FDA. It is based on fenofibrate and digoxin (the active ingredients of Antara and Digoxin, respectively), and Antara and Digoxin (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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