Arixtra and Cytoxan drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Arixtra (fondaparinux sodium) and Cytoxan (cyclophosphamide). Common drug interactions include back pain among females and abdominal discomfort among males.
The phase IV clinical study analyzes what interactions people have when they take Arixtra and Cytoxan. It is created by eHealthMe based on reports of 17 people who take the same drugs from the FDA, and is updated regularly.
What is Arixtra?
Arixtra has active ingredients of fondaparinux sodium. It is often used in deep venous thrombosis. eHealthMe is studying from 9,830 Arixtra users. Check the latest studies of Arixtra.
What is Cytoxan?
Cytoxan has active ingredients of cyclophosphamide. It is often used in breast cancer. eHealthMe is studying from 19,693 Cytoxan users. Check the latest studies of Cytoxan.
17 people who take Arixtra and Cytoxan together, and have interactions are studied.

What are the common drug interactions of Arixtra and Cytoxan, by gender? *:
female:
- Back pain
- Blood iron increased
- Bone lesion (bone with abnormalities. bone lesions can result from growth formations, infections, or injuries)
- Bone pain
- Breast cancer recurrent
- Cardiac murmur (an heart sound in valve abnormality)
- Cardiomegaly (increased size of heart than normal)
- Chest pain
- Chronic obstructive pulmonary disease (a progressive disease that makes it hard to breathe)
- Clostridium difficile colitis (inflammation of colon by clostridium difficile bacteria infection)
male:
- Abdominal discomfort
- Diarrhoea
- Back pain
- Bowel movement irregularity
- Cellulitis (infection under the skin)
- Cerebral atrophy (decrement in size of brain)
- Cerebral infarction (less blood supply to brain resulting tissue damage)
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Decreased appetite
What are the common drug interactions of Arixtra and Cytoxan, by age (0-1 to 60+)? *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Acute myeloid leukaemia (acute cancer in which the bone marrow makes abnormal myeloblasts)
- Acute respiratory distress syndrome
- Anaemia (lack of blood)
- Anxiety
- Aortic stenosis (obstruction to the outflow of blood from the left ventricle into the aorta)
- Application site burn
- Arthralgia (joint pain)
- Asthenia (weakness)
- Atelectasis (partial or complete collapse of the lung)
- Avulsion fracture (bone fracture)
50-59:
- Fatigue (feeling of tiredness)
- Arthralgia (joint pain)
- Clostridium difficile colitis (inflammation of colon by clostridium difficile bacteria infection)
- Diarrhoea
- Erythema (redness of the skin)
- Febrile neutropenia (fever with reduced white blood cells)
- Memory impairment
- Nausea (feeling of having an urge to vomit)
- Oedema peripheral (superficial swelling)
- Pain
60+:
- Abdominal discomfort
- Abdominal pain
- Cellulitis (infection under the skin)
- Cerebral atrophy (decrement in size of brain)
- Cerebral infarction (less blood supply to brain resulting tissue damage)
- Cerebrovascular accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)
- Cholelithiasis (the presence or formation of gallstones in the gallbladder or bile ducts)
- Decreased appetite
- Dermal cyst
- Diarrhoea
What are the existing conditions these people have? *
- Multiple Myeloma (cancer of the plasma cells): 6 people, 35.29%
- Gastroesophageal Reflux Disease (a condition in which stomach contents leak backward from the stomach into the oesophagus): 3 people, 17.65%
- Insomnia (sleeplessness): 2 people, 11.76%
- Pain: 2 people, 11.76%
- Depression: 2 people, 11.76%
- Fluid Retention (an abnormal accumulation of fluid in the blood): 2 people, 11.76%
- Hyperlipidaemia (presence of excess lipids in the blood): 2 people, 11.76%
- Hypercalcaemia (elevated calcium (ca+) level in the blood): 1 person, 5.88%
- Anaemia Of Malignant Disease: 1 person, 5.88%
- Blood Magnesium Decreased: 1 person, 5.88%
* Approximation only. Some reports may have incomplete information.
Do you take Arixtra and Cytoxan?
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Related studies:
Effectiveness of, side effects of, and alternative drugs to the 2 drugs:
Browse all drug interactions of Arixtra and Cytoxan:
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 Arixtra:
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 Cytoxan:
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 Arixtra 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 Cytoxan 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
- Hu P, Lu L, Hu B, Deng F, Fei WJ, "Cyclophosphamide‐Induced Hypertensive Encephalopathy in a Young Girl With Lupus", The Journal of Clinical Hypertension, 2012 Apr .
- Hu P, Lu L, Hu B, Deng F, Fei WJ, "Cyclophosphamide‐Induced Hypertensive Encephalopathy in a Young Girl With Lupus", The Journal of Clinical Hypertension, 2012 Apr .
How the study uses the data?
The study uses data from the FDA. It is based on fondaparinux sodium and cyclophosphamide (the active ingredients of Arixtra and Cytoxan, respectively), and Arixtra and Cytoxan (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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