Norepinephrine bitartrate and Diprivan drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Norepinephrine bitartrate (norepinephrine bitartrate) and Diprivan (propofol). Common drug interactions include bundle branch block left among females and burkholderia test positive among males.
The phase IV clinical study analyzes what interactions people have when they take Norepinephrine bitartrate and Diprivan. It is created by eHealthMe based on reports of 38 people who take the same drugs from the FDA, and is updated regularly.
What is Norepinephrine bitartrate?
Norepinephrine bitartrate has active ingredients of norepinephrine bitartrate. eHealthMe is studying from 2,370 Norepinephrine bitartrate users. Check the latest studies of Norepinephrine bitartrate.
What is Diprivan?
Diprivan has active ingredients of propofol. eHealthMe is studying from 6,496 Diprivan users. Check the latest studies of Diprivan.
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 >>>.
38 people who take Norepinephrine bitartrate and Diprivan together, and have interactions are studied.

What are the common drug interactions of Norepinephrine Bitartrate and Diprivan, by gender? *:
female:
- Bundle branch block left (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the left ventricle)
- Bundle branch block right (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the right ventricle)
- Cardiac arrest
- Cardiac failure
- Gastric ulcer perforation (stomach hole due to ulcer)
- Hypotension (abnormally low blood pressure)
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
- Propofol infusion syndrome
- Pulmonary fibrosis (formation or development of excess fibrous connective tissue (fibrosis) in the lungs)
- Thrombocytopenia (decrease of platelets in blood)
male:
- Burkholderia test positive
- Gamma-glutamyltransferase increased
- Dyspnoea (difficult or laboured respiration)
- Ejection fraction decreased (systolic heart failure)
- Insomnia (sleeplessness)
- Intestinal ischaemia (decreased supply of oxygenated blood to the intestines)
- Intraventricular haemorrhage (intraventricular bleeding)
- Platelet count decreased
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Respiratory rate decreased (less breathing rate/min)
What are the common drug interactions of Norepinephrine Bitartrate and Diprivan, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
- Platelet count decreased
- Renal failure acute (rapid kidney dysfunction)
- Respiratory failure (inadequate gas exchange by the respiratory system)
- Blood fibrinogen increased
- Haemoglobin decreased
- Haemorrhagic stroke (stroke caused by the rupture of a blood vessel in the brain)
- Hemiparesis (weakness on one side of the body)
- Hemiplegia (paralysis of one side of the body)
- Meningitis meningococcal (a bacterial infection of the membranes covering the brain and spinal cord (meninges))
- Neisseria infection (a bacterial infection)
20-29:
n/a
30-39:
- Atrioventricular block first degree (heart block first degree)
- Blood triglycerides increased
- Bundle branch block left (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the left ventricle)
- Bundle branch block right (absence of transmission of electric impulses from the atrioventricular (av) bundle of his to the right ventricle)
- Cardiac arrest
- Hypotension (abnormally low blood pressure)
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
- Propofol infusion syndrome
40-49:
- Platelet count decreased
- Propofol infusion syndrome
50-59:
- Death
- Injury
- Oedema (fluid collection in tissue)
- Pain
- Renal failure (kidney dysfunction)
- Renal failure acute (rapid kidney dysfunction)
- Alanine aminotransferase increased
- Blood bilirubin increased
- Blood creatinine increased
- Lactic acidosis (low ph in body tissues)
60+:
- Gamma-glutamyltransferase increased
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Blood pressure decreased
- Convulsions (muscles contract and relax rapidly and repeatedly, resulting in an uncontrolled of muscles contract and relax rapidly and repeatedly)
- Dyskinesia (abnormality or impairment of voluntary movement)
- Dyspnoea (difficult or laboured respiration)
- Nausea (feeling of having an urge to vomit)
- Oxygen saturation decreased
- Renal failure (kidney dysfunction)
- Septic shock (shock due to blood infection)
What are the existing conditions these people have? *
- Sedation: 9 people, 23.68%
- Pharyngitis (inflammation of the pharynx, causing a sore throat): 3 people, 7.89%
- Idiopathic Pulmonary Fibrosis (chronic lung disease): 3 people, 7.89%
- Hypotension (abnormally low blood pressure): 3 people, 7.89%
- Coronary Revascularisation: 3 people, 7.89%
- Septic Shock (shock due to blood infection): 2 people, 5.26%
- Pneumonia Staphylococcal (pneumonia staphylococcal infections are usually caused by the organism staphylococcus aureus): 2 people, 5.26%
- Pain: 2 people, 5.26%
- Meningitis Meningococcal (a bacterial infection of the membranes covering the brain and spinal cord (meninges)): 2 people, 5.26%
- Insomnia (sleeplessness): 2 people, 5.26%
* Approximation only. Some reports may have incomplete information.
Do you take Norepinephrine bitartrate and Diprivan?
- 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:
- Norepinephrine bitartrate (2,370 reports)
- Diprivan (6,496 reports)
Browse all drug interactions of Norepinephrine bitartrate and Diprivan:
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 Norepinephrine bitartrate:
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 Diprivan:
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 Norepinephrine bitartrate 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 Diprivan 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 norepinephrine bitartrate and propofol (the active ingredients of Norepinephrine bitartrate and Diprivan, respectively), and Norepinephrine bitartrate and Diprivan (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.
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