Digitalis and Furosemide drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Digitalis (digitalis) and Furosemide (furosemide). Common drug interactions include blood glucose increased among females and dyspnoea among males.
The phase IV clinical study analyzes what interactions people have when they take Digitalis and Furosemide. It is created by eHealthMe based on reports of 50 people who take the same drugs from the FDA, and is updated regularly.
What is Digitalis?
Digitalis has active ingredients of digitalis. eHealthMe is studying from 332 Digitalis users. Check the latest studies of Digitalis.
What is Furosemide?
Furosemide has active ingredients of furosemide. It is often used in fluid retention. eHealthMe is studying from 316,095 Furosemide users. Check the latest studies of Furosemide.
50 people who take Digitalis and Furosemide together, and have interactions are studied.

What are the common drug interactions of Digitalis and Furosemide, by gender? *:
female:
- Blood glucose increased
- Blood potassium decreased
- Blood pressure decreased
- Bradycardia (abnormally slow heart action)
- Bronchiectasis (abnormal widening of the bronchi or their branches, causing a risk of infection)
- Cardiac failure chronic
- Cardiomyopathy (weakening of the heart muscle)
- Confusional state
- Death
- Decreased appetite
male:
- Dyspnoea (difficult or laboured respiration)
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Oedema peripheral (superficial swelling)
- Pulmonary congestion (congestion in the lungs)
- Renal impairment (severely reduced kidney function)
- Troponin increased
- Atrioventricular block complete (heart block complete)
- Bone marrow failure
- Foetal exposure during pregnancy (exposing your unborn child to contraindicated in pregnancy leads birth defect)
What are the common drug interactions of Digitalis and Furosemide, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Atrioventricular block (heart block)
- Cardiac failure
- Maternal exposure during pregnancy (use of substance during pregnancy)
- Premature delivery
- Ventricular tachycardia (rapid heartbeat that originates in one of the lower chambers (the ventricles) of the heart)
- Atrioventricular block second degree (heart block second degree)
40-49:
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Cardiac failure
- Death
- Hypotension (abnormally low blood pressure)
- Ischaemic cardiomyopathy (weakness in the muscle of the heart due to inadequate oxygen delivery to the myocardium with coronary artery disease)
- Liver injury
- Oedema peripheral (superficial swelling)
- Renal injury (kidney injury)
50-59:
- Acute right ventricular failure (acute heart attack)
- Atrial fibrillation (fibrillation of the muscles of the atria of the heart)
- Atrial flutter (an abnormal heart rhythm that occurs in the atria of the heart)
- Atrioventricular block complete (heart block complete)
- Cardiac failure acute
- Dyspnoea (difficult or laboured respiration)
- Fluid overload (too much fluid in the blood)
- Oedema (fluid collection in tissue)
- Oxygen saturation decreased
- Palpitations (feelings or sensations that your heart is pounding or racing)
60+:
- Hypotension (abnormally low blood pressure)
- Cardiac failure
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Bone marrow failure
- Bradycardia (abnormally slow heart action)
- Coma (state of unconsciousness lasting more than six hours)
- Constipation
- Decreased appetite
- Diverticulitis (digestive disease which involves the formation of pouches (diverticula) within the bowel wall)
- Dizziness
What are the existing conditions these people have? *
- Atrial Fibrillation/flutter (atrial fibrillation and flutter are abnormal heart rhythms in which the atria, or upper chambers of the heart, are out of sync with the ventricles): 10 people, 20.00%
- Cardiac Failure Chronic: 5 people, 10.00%
- Cardiac Failure: 5 people, 10.00%
- Cardiac Failure Congestive: 4 people, 8.00%
- Insomnia (sleeplessness): 3 people, 6.00%
* Approximation only. Some reports may have incomplete information.
Do you take Digitalis and Furosemide?
- 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:
- Digitalis (332 reports)
- Furosemide (316,095 reports)
Browse all drug interactions of Digitalis and Furosemide:
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 Digitalis:
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 Furosemide:
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 Digitalis 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 Furosemide 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
- Ochoa PS, Fisher T, "A 7‐Year Case of Furosemide‐Induced Immune Thrombocytopenia", Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 2013 Jul .
- Ochoa PS, Fisher T, "A 7‐Year Case of Furosemide‐Induced Immune Thrombocytopenia", Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, 2013 Jul .
How the study uses the data?
The study uses data from the FDA. It is based on digitalis and furosemide (the active ingredients of Digitalis and Furosemide, respectively), and Digitalis and Furosemide (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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