Digoxin and Zerit drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Digoxin (digoxin) and Zerit (stavudine). Common drug interactions include chronic kidney disease among females and abdominal pain among males.
The phase IV clinical study analyzes what interactions people have when they take Digoxin and Zerit. It is created by eHealthMe based on reports of 31 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Zerit?
Zerit has active ingredients of stavudine. eHealthMe is studying from 9,912 Zerit users. Check the latest studies of Zerit.
31 people who take Digoxin and Zerit together, and have interactions are studied.

What are the common drug interactions of Digoxin and Zerit, by gender? *:
female:
- Chronic kidney disease
- Death
- Emotional distress
- Hypersensitivity
- Pain
- Renal failure (kidney dysfunction)
- Tooth loss
- Bradycardia (abnormally slow heart action)
- Cholestasis (a condition where bile cannot flow from the liver to the duodenum)
- Diarrhoea
male:
- Abdominal pain
- Pancreatitis (inflammation of pancreas)
- Malaise (a feeling of general discomfort or uneasiness)
- Oesophageal candidiasis (fungal infection of oesophagus)
- Abdominal pain upper
- Abdominal tenderness
- Anorexia (eating disorder characterized by immoderate food restriction and irrational fear of gaining weight)
- Atrioventricular block (heart block)
- Bacteraemia (presence of bacteria in the blood)
- Blood pressure decreased
What are the common drug interactions of Digoxin and Zerit, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
- Cardiomyopathy (weakening of the heart muscle)
10-19:
- Cholestasis (a condition where bile cannot flow from the liver to the duodenum)
- Diarrhoea
- Hepatomegaly (abnormal enlargement of the liver)
- Pancreatitis (inflammation of pancreas)
- Rash maculo-papular (red area on the skin that is covered with small confluent bumps)
20-29:
- Face oedema (swelling of face)
- Pruritus (severe itching of the skin)
- Rash
- Dermatitis (inflammation of the skin resulting from direct irritation by an external agent or an allergic reaction to it)
- Hypersensitivity
- Disease progression
- Drug hypersensitivity
- Multi-organ failure (multisystem organ failure)
- Pulmonary hypertension (increase in blood pressure in the lung artery)
- Swelling face
30-39:
- Atrioventricular block complete (heart block complete)
- Bradycardia (abnormally slow heart action)
- Congestive cardiomyopathy (weakening of heart muscle)
- Coronary artery occlusion (complete obstruction of blood flow in a coronary artery)
- Cough
- Dyspnoea (difficult or laboured respiration)
- Dyspnoea exertional (breathlessness or shortness of breath)
- Heart rate decreased
- Hepatomegaly (abnormal enlargement of the liver)
- Hypotension (abnormally low blood pressure)
40-49:
- Pancreatitis (inflammation of pancreas)
- Abdominal pain
- Body temperature increased
- Cardiac arrest
- Cardiac failure congestive
- Lactic acidosis (low ph in body tissues)
- Abdominal pain upper
- Abdominal tenderness
- Anorexia (eating disorder characterized by immoderate food restriction and irrational fear of gaining weight)
- Bacteraemia (presence of bacteria in the blood)
50-59:
- Fibula fracture
- Ankle fracture
- Appetite increased (increased appetite is when you want to eat much more often or in larger quantities than your body requires)
- Blood alkaline phosphatase nos increased
- Blood bilirubin increased
- Blood cholesterol increased
- Blood glucose increased
- Blood triglycerides increased
- Cardiac disorder
- Cardiomyopathy (weakening of the heart muscle)
60+:
n/a
What are the existing conditions these people have? *
- Hiv Infection: 5 people, 16.13%
- Pulmonary Hypertension Primary (increase in blood pressure in the lung artery with no cause): 4 people, 12.90%
* Approximation only. Some reports may have incomplete information.
Do you take Digoxin and Zerit?
- 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 Digoxin and Zerit:
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 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 side effects of Zerit:
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 zBrowse all interactions between Zerit 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 digoxin and stavudine (the active ingredients of Digoxin and Zerit, respectively), and Digoxin and Zerit (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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