Ornithine and Enoxaparin sodium drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Ornithine (ornithine) and Enoxaparin sodium (enoxaparin sodium). Common drug interactions include thrombocytopenia among females and anaemia among males.
The phase IV clinical study analyzes what interactions people have when they take Ornithine and Enoxaparin sodium. It is created by eHealthMe based on reports of 22 people who take the same drugs from the FDA, and is updated regularly.
What is Ornithine?
Ornithine has active ingredients of ornithine. eHealthMe is studying from 591 Ornithine users. Check the latest studies of Ornithine.
What is Enoxaparin sodium?
Enoxaparin sodium has active ingredients of enoxaparin sodium. It is often used in deep venous thrombosis. eHealthMe is studying from 24,181 Enoxaparin sodium users. Check the latest studies of Enoxaparin sodium.
22 people who take Ornithine and Enoxaparin sodium together, and have interactions are studied.

What are the common drug interactions of Ornithine and Enoxaparin Sodium, by gender? *:
female:
- Thrombocytopenia (decrease of platelets in blood)
- Acidosis (build-up of carbon dioxide in the blood)
- Anisocytosis (patient's red blood cells are of unequal size)
- Blood bilirubin increased
- Blood creatinine increased
- Blood pressure decreased
- Blood urea increased
- Bradycardia (abnormally slow heart action)
- Creatinine renal clearance decreased
- Drug level above therapeutic
male:
- Anaemia (lack of blood)
- Pleural effusion (water on the lungs)
- Arteriosclerosis coronary artery (thickening and hardening of arteries- coronary artery)
- Ascites (accumulation of fluid in the abdominal cavity)
- Atelectasis (partial or complete collapse of the lung)
- Bile duct necrosis
- Bile duct stenosis (abnormal narrowing of the common bile duct)
- Biliary tract disorder
- Blood bilirubin increased
- Bronchopneumonia (inflammation of the lungs, arising in the bronchi or bronchioles)
What are the common drug interactions of Ornithine and Enoxaparin Sodium, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
- Thrombocytopenia (decrease of platelets in blood)
30-39:
- Anuria (failure of the kidneys to produce urine)
- Arteriosclerosis coronary artery (thickening and hardening of arteries- coronary artery)
- Atelectasis (partial or complete collapse of the lung)
- Bile duct necrosis
- Bile duct stenosis (abnormal narrowing of the common bile duct)
- Biliary tract disorder
- Blood bilirubin increased
- Bronchopneumonia (inflammation of the lungs, arising in the bronchi or bronchioles)
- C-reactive protein increased
- Cardiac failure
40-49:
n/a
50-59:
- Anaemia (lack of blood)
- Ascites (accumulation of fluid in the abdominal cavity)
- Diabetes mellitus (diabetes, caused by a deficiency of the pancreatic hormone insulin)
- Hepatic cirrhosis (chronic liver disease characterized by replacement of liver tissue by fibrosis, scar tissue)
- Hepatic encephalopathy (spectrum of neuropsychiatric abnormalities in patients with liver failure)
- Hepatorenal syndrome (renal failure in patients with advanced chronic liver disease)
- Hyperkalaemia (damage to or disease of the kidney)
- Metabolic acidosis (body produces too much acid, or when the kidneys are not removing enough acid from the body)
- Oedema peripheral (superficial swelling)
- Pleural effusion (water on the lungs)
60+:
- Anaemia (lack of blood)
- Shock haemorrhagic (a life-threatening condition with symptoms like low blood pressure, weakness, shallow breathing, cold, clammy skin due to excess bleeding)
- Anisocytosis (patient's red blood cells are of unequal size)
- Blood bilirubin increased
- Blood creatinine increased
- Blood pressure decreased
- Blood urea increased
- Bradycardia (abnormally slow heart action)
- Creatinine renal clearance decreased
- Cytokine release syndrome (immediate complication occurring with the use of anti-t cell antibody infusions)
What are the existing conditions these people have? *
- Cardiac Failure: 6 people, 27.27%
- Hypokalemia (low potassium): 6 people, 27.27%
- Anaemia (lack of blood): 5 people, 22.73%
- Constipation: 5 people, 22.73%
- Rashes (redness): 4 people, 18.18%
- 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): 4 people, 18.18%
- Chronic Obstructive Pulmonary Disease (a progressive disease that makes it hard to breathe): 4 people, 18.18%
- High Blood Pressure: 4 people, 18.18%
- Type 2 Diabetes: 3 people, 13.64%
- Hyperglycemia (high blood sugar): 3 people, 13.64%
* Approximation only. Some reports may have incomplete information.
Do you take Ornithine and Enoxaparin sodium?
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- 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:
- Ornithine (591 reports)
- Enoxaparin sodium (24,181 reports)
Browse all drug interactions of Ornithine and Enoxaparin sodium:
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 Ornithine:
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 Enoxaparin sodium:
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 Ornithine 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 Enoxaparin sodium 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 ornithine and enoxaparin sodium (the active ingredients of Ornithine and Enoxaparin sodium, respectively), and Ornithine and Enoxaparin sodium (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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