Furosemide and Angiomax drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Furosemide (furosemide) and Angiomax (bivalirudin). Common drug interactions include muscular weakness among females and renal failure among males.
The phase IV clinical study analyzes what interactions people have when they take Furosemide and Angiomax. It is created by eHealthMe based on reports of 51 people who take the same drugs from the FDA, and is updated regularly.
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.
What is Angiomax?
Angiomax has active ingredients of bivalirudin. eHealthMe is studying from 2,301 Angiomax users. Check the latest studies of Angiomax.
51 people who take Furosemide and Angiomax together, and have interactions are studied.

What are the common drug interactions of Furosemide and Angiomax, by gender? *:
female:
- Muscular weakness (muscle weakness)
- Nausea (feeling of having an urge to vomit)
- Neutropenia (an abnormally low number of neutrophils)
- Oxygen consumption increased
- Pain
- Post procedural haematoma (post procedural clotting of blood)
- Pulmonary alveolar haemorrhage (acute bleeding)
- Pulmonary hypertension (increase in blood pressure in the lung artery)
- Pulse pressure decreased
- Renal failure acute (rapid kidney dysfunction)
male:
- Renal failure (kidney dysfunction)
- Coronary artery thrombosis (clot formation in coronary artery)
- Chronic kidney disease
- Coronary artery stenosis (narrowing of coronary artery)
- Diarrhoea
- Dizziness postural
- Dyspnoea (difficult or laboured respiration)
- Epistaxis (bleed from the nose)
- Hyponatraemia (abnormally low level of sodium in the blood; associated with dehydration)
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
What are the common drug interactions of Furosemide and Angiomax, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Activated partial thromboplastin time prolonged
- International normalised ratio increased
- Pleural effusion (water on the lungs)
30-39:
- Chronic kidney disease
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal failure (kidney dysfunction)
40-49:
- Death
50-59:
- Drug hypersensitivity
- Dyspnoea (difficult or laboured respiration)
- Neck pain
- Oedema peripheral (superficial swelling)
- Renal failure (kidney dysfunction)
- Serum sickness (hypersensitivity reaction that results from the injection of heterologous or foreign protein or serum)
- Thrombosis (formation of a blood clot inside a blood vessel)
- Bronchitis (inflammation of the mucous membrane in the bronchial tubes)
- Hypotension (abnormally low blood pressure)
- Pain in extremity
60+:
- Renal failure (kidney dysfunction)
- Coronary artery thrombosis (clot formation in coronary artery)
- Nephrogenic anaemia (anaemia due to kidney disease)
- Renal injury (kidney injury)
- Anuria (failure of the kidneys to produce urine)
- Chest pain
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
- Platelet count decreased
- Renal failure acute (rapid kidney dysfunction)
- Respiratory failure (inadequate gas exchange by the respiratory system)
What are the existing conditions these people have? *
- High Blood Pressure: 8 people, 15.69%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 8 people, 15.69%
- 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): 6 people, 11.76%
- Percutaneous Coronary Intervention: 5 people, 9.80%
- Acute Myocardial Infarction (acute heart attack): 5 people, 9.80%
- Acute Coronary Syndrome (acute chest pain and other symptoms that happen because the heart does not get blood): 5 people, 9.80%
- Pain: 4 people, 7.84%
- Ventricular Dysfunction (heart dysfunction): 3 people, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Furosemide and Angiomax?
- 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:
- Furosemide (316,095 reports)
- Angiomax (2,301 reports)
Browse all drug interactions of Furosemide and Angiomax:
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 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 side effects of Angiomax:
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 zBrowse all interactions between Angiomax 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 furosemide and bivalirudin (the active ingredients of Furosemide and Angiomax, respectively), and Furosemide and Angiomax (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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