Tenormin and Triatec drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Tenormin (atenolol) and Triatec (ramipril). Common drug interactions include cerebral haematoma among females and aplastic anaemia among males.
The phase IV clinical study analyzes what interactions people have when they take Tenormin and Triatec. It is created by eHealthMe based on reports of 74 people who take the same drugs from the FDA, and is updated regularly.
What is Tenormin?
Tenormin has active ingredients of atenolol. It is often used in high blood pressure. eHealthMe is studying from 20,474 Tenormin users. Check the latest studies of Tenormin.
What is Triatec?
Triatec has active ingredients of ramipril. eHealthMe is studying from 4,133 Triatec users. Check the latest studies of Triatec.
74 people who take Tenormin and Triatec together, and have interactions are studied.

What are the common drug interactions of Tenormin and Triatec, by gender? *:
female:
- Cerebral haematoma (collection of blood in brain)
- Cheilitis (infection of lips)
- Circulatory collapse
- Confusion
- Conjunctival hyperaemia (congestion of conjunctival vessels)
- Conjunctivitis (pink eye)
- Depressed level of consciousness
- Dysphagia (a condition in which swallowing is difficult or painful)
- Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures)
- Erythema multiforme (a type of hypersensitivity reaction)
male:
- Aplastic anaemia (blood disorder in which the body's bone marrow doesn't make enough new blood cells)
- Asthenia (weakness)
- Cytolytic hepatitis (dissolution or destruction of a liver cell)
- Dizziness
- Extrasystoles
- Fall
- Myocardial infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)
- Photosensitivity reaction
- Pleural effusion (water on the lungs)
- Abdominal pain
What are the common drug interactions of Tenormin and Triatec, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Hypogammaglobulinaemia (an abnormally low concentration of gamma globulin in the blood and increased risk of infection)
- Lymphopenia (an abnormally low level of lymphocytes in the blood)
- Transaminases increased
30-39:
- Aplastic anaemia (blood disorder in which the body's bone marrow doesn't make enough new blood cells)
- Leukocytosis (increased white blood cells)
- Normochromic normocytic anaemia (forms of anaemia in which the average size and haemoglobin content of the red blood cells are within normal limits)
40-49:
- Haemolytic anaemia (anaemia due to haemolysis)
- Pulmonary toxicity (side effects on the lungs)
- Rectal haemorrhage (bleeding from anus)
- Respiratory distress (difficulty in breathing)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Thrombocytopenia (decrease of platelets in blood)
50-59:
- Cerebral haematoma (collection of blood in brain)
- Chest pain
- Convulsion (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled shaking of the body)
- Cytomegalovirus infection
- Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures)
- Fall
- Hepatitis b antibody positive
- Hypercholesterolaemia (high levels of cholesterol in the blood)
- Hypertriglyceridaemia (excess of triglycerides in the blood)
- Infectious mononucleosis (infection usually caused by the epstein-barr virus)
60+:
- Pancreatitis acute (sudden inflammation of pancreas)
- Vomiting
- Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect)
- Abdominal pain
- Asthenia (weakness)
- Atrioventricular block complete (heart block complete)
- Carpal tunnel syndrome (nerve compression at wrist results numbness weakness, pain , swelling)
- Cholestasis (a condition where bile cannot flow from the liver to the duodenum)
- Cytolytic hepatitis (dissolution or destruction of a liver cell)
- Dizziness
What are the existing conditions these people have? *
- Type 2 Diabetes: 8 people, 10.81%
* Approximation only. Some reports may have incomplete information.
Do you take Tenormin and Triatec?
- 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 Tenormin and Triatec:
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 Tenormin:
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 Triatec:
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 Tenormin 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 Triatec 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 zHow the study uses the data?
The study uses data from the FDA. It is based on atenolol and ramipril (the active ingredients of Tenormin and Triatec, respectively), and Tenormin and Triatec (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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