Tolvaptan and Coreg drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Tolvaptan (tolvaptan) and Coreg (carvedilol). Common drug interactions include blood iron decreased among females and cardiac failure congestive among males.
The phase IV clinical study analyzes what interactions people have when they take Tolvaptan and Coreg. It is created by eHealthMe based on reports of 30 people who take the same drugs from the FDA, and is updated regularly.
What is Tolvaptan?
Tolvaptan has active ingredients of tolvaptan. eHealthMe is studying from 5,685 Tolvaptan users. Check the latest studies of Tolvaptan.
What is Coreg?
Coreg has active ingredients of carvedilol. It is often used in high blood pressure. eHealthMe is studying from 49,584 Coreg users. Check the latest studies of Coreg.
eHealthMe: drug outcomes in the real world
eHealthMe runs one of the largest post-marketing drug safety studies in the world. We study millions of patients and 5,000 more each day. Our data-driven phase IV clinical trials have been referenced on 800+ peer-reviewed medical publications including The Lancet, Mayo Clinic Proceedings, and Nature. Tools to study our phase IV findings are available to the public, anonymous and free >>>.
30 people who take Tolvaptan and Coreg together, and have interactions are studied.

What are the common drug interactions of Tolvaptan and Coreg, by gender? *:
female:
- Blood iron decreased
- Blood parathyroid hormone increased
- Blood uric acid increased
- Cardiac arrest
- Constipation
- Cystatin c increased
- Decreased appetite
- Discomfort
- Early satiety (feeling full before completing a normal sized meal)
- Gastric varices
male:
- Cardiac failure congestive
- Hypotension (abnormally low blood pressure)
- Multiple injuries
- Surgery
- Blood chloride decreased
- Blood creatinine decreased
- Blood glucose increased
- Blood potassium increased
- Blood sodium decreased
- Carbon dioxide decreased
What are the common drug interactions of Tolvaptan and Coreg, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
- Anion gap increased
- Blood albumin decreased
- Blood calcium increased
- Blood chloride increased
- Blood creatinine increased
- Blood osmolarity increased
- Blood potassium increased
- Blood urea increased
- Blood uric acid increased
- Carbon dioxide decreased
40-49:
- Abdominal distension
- Blood creatinine increased
- Blood potassium decreased
- Cardiac failure congestive
- Hepatomegaly (abnormal enlargement of the liver)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Oedema (fluid collection in tissue)
50-59:
- Muscle atrophy (a decrease in the mass of the muscle)
- Myocarditis (inflammation of heart muscle myocardium)
- Osteoporosis postmenopausal (weak bone with possibility to break after stopped menstrual cycles)
- Platelet count decreased
- Pleural effusion (water on the lungs)
- Portal hypertension (increase in the blood pressure within a system of veins called the portal venous system)
- Procedural haemorrhage (procedural bleeding)
- Pulmonary congestion (congestion in the lungs)
- Pulmonary valve disease
- Pulseless electrical activity
60+:
- Cardiac failure congestive
- Hypotension (abnormally low blood pressure)
- Renal failure (kidney dysfunction)
- Dyspnoea (difficult or laboured respiration)
- Injury
- Cardiomegaly (increased size of heart than normal)
- Cough
- Renal failure acute (rapid kidney dysfunction)
- Alanine aminotransferase increased
- Anaemia (lack of blood)
What are the existing conditions these people have? *
- Cardiac Failure Congestive: 14 people, 46.67%
- Hyponatremia (abnormally low level of sodium in the blood; associated with dehydration): 4 people, 13.33%
- Blood Sodium Decreased: 2 people, 6.67%
* Approximation only. Some reports may have incomplete information.
Do you take Tolvaptan and Coreg?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Tolvaptan and Coreg:
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 Tolvaptan:
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 Coreg:
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 Tolvaptan 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 Coreg 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
- Barold, S. S., & Upton, S. , "Hyperkalemia Induced by the Sequential Administration of Metoprolol and Carvedilol", Case reports in cardiology, 2018 Jan .
- Kim MS, Baek IH, "Effect of dronedarone on the pharmacokinetics of carvedilol following oral administration to rats", European Journal of Pharmaceutical Sciences, 2018 Jan .
- Barold, S. S., & Upton, S. , "Hyperkalemia Induced by the Sequential Administration of Metoprolol and Carvedilol", Case reports in cardiology, 2018 Jan .
- Kim MS, Baek IH, "Effect of dronedarone on the pharmacokinetics of carvedilol following oral administration to rats", European Journal of Pharmaceutical Sciences, 2018 Jan .
How the study uses the data?
The study uses data from the FDA. It is based on tolvaptan and carvedilol (the active ingredients of Tolvaptan and Coreg, respectively), and Tolvaptan and Coreg (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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