Propranolol hydrochloride and Liver function test abnormal - a phase IV clinical study of FDA data

Summary:

Liver function test abnormal is reported as a side effect among people who take Propranolol hydrochloride (propranolol hydrochloride), especially for people who are female, 40-49 old, have been taking the drug for 1 - 6 months also take Sumatriptan Succinate, and have Pain.

The phase IV clinical study analyzes which people have Liver function test abnormal when taking Propranolol hydrochloride. It is created by eHealthMe based on reports of 9,728 people who have side effects when taking Propranolol hydrochloride from the FDA, and is updated regularly.

What is Propranolol hydrochloride?

Propranolol hydrochloride has active ingredients of propranolol hydrochloride. It is often used in stress and anxiety. eHealthMe is studying from 12,026 Propranolol hydrochloride users. Check the latest studies of Propranolol hydrochloride.

What is Liver function test abnormal?

Liver function test abnormal is found to be associated with 1,502 drugs and 1,962 conditions by eHealthMe. Check the latest studies of Liver function test abnormal.

On Jul, 13, 2026

9,728 people reported to have side effects when taking Propranolol hydrochloride.
Among them, 17 people (0.17%) have Liver function test abnormal.

Could Propranolol hydrochloride cause Liver function test abnormal?

Among these 17 people:

How long have people been on Propranolol hydrochloride when they have Liver function test abnormal? *

What is the gender of people who have Liver function test abnormal when taking Propranolol hydrochloride? *

female: 61.54 %
male: 38.46 %

What is the age of people who have Liver function test abnormal when taking Propranolol hydrochloride? *

What are other drugs people take besides Propranolol hydrochloride? *

What are other side effects people have besides Liver function test abnormal? *

Blood Glucose Increased: 4 people, 23.53%
Rashes (redness): 3 people, 17.65%
Jaundice - Yellow Skin (a yellowish pigmentation of the skin): 3 people, 17.65%
Blood Alkaline Phosphatase Increased: 3 people, 17.65%
Fatigue (feeling of tiredness): 3 people, 17.65%
High Blood Cholesterol: 3 people, 17.65%
White Blood Cell Count Decreased: 3 people, 17.65%
Hair Loss: 2 people, 11.76%
Feeling Abnormal: 2 people, 11.76%
Fever: 2 people, 11.76%

What are the existing conditions these people have? *

Pain: 2 people, 11.76%
Vertigo Cns Origin: 1 person, 5.88%
Juvenile Rheumatoid Arthritis (joint inflammation in children due to systemic disease): 1 person, 5.88%
Fluid Retention (an abnormal accumulation of fluid in the blood): 1 person, 5.88%
Headache (pain in head): 1 person, 5.88%
Hepatic Cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue): 1 person, 5.88%
High Blood Cholesterol: 1 person, 5.88%
Insomnia (sleeplessness): 1 person, 5.88%
Juvenile Arthritis (arthritis-related condition that develops in children or teenagers): 1 person, 5.88%
Leukaemia (blood or bone marrow cancer): 1 person, 5.88%

* Approximation only. Some reports may have incomplete information.

Do you take Propranolol hydrochloride and have Liver function test abnormal?

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Related studies:

Effectiveness of, long term effects of, and alternative drugs to Propranolol hydrochloride:

Propranolol hydrochloride (12,026 reports)

Browse all side effects of Propranolol hydrochloride:

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Browse all the drugs that are associated with Liver function test abnormal:

Liver function test abnormal (1,502 drugs)

Browse all the conditions that are associated with Liver function test abnormal:

Liver function test abnormal (1,962 conditions)

How the study uses the data?

The study uses data from the FDA. It is based on propranolol hydrochloride (the active ingredients of Propranolol hydrochloride) and Propranolol hydrochloride (the brand name). 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.