Arixtra and Zoledronic acid drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among people who take Arixtra (fondaparinux sodium) and Zoledronic acid (zoledronic acid). Common drug interactions include vomiting among females and febrile neutropenia among males.
The phase IV clinical study analyzes what interactions people have when they take Arixtra and Zoledronic acid. It is created by eHealthMe based on reports of 49 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 Zoledronic acid?
Zoledronic acid has active ingredients of zoledronic acid. eHealthMe is studying from 28,485 Zoledronic acid users. Check the latest studies of Zoledronic acid.
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 >>>.
49 people who take Arixtra and Zoledronic acid together, and have interactions are studied.

What are the common drug interactions of Arixtra and Zoledronic Acid, by gender? *:
female:
- Vomiting
- Dysphagia (a condition in which swallowing is difficult or painful)
- Nausea (feeling of having an urge to vomit)
- Pulpitis dental (inflammation of the tooth pulp)
- Sensory disturbance (sense disturbance)
- Thrombosis (formation of a blood clot inside a blood vessel)
- Weight decreased
- Hypertension (high blood pressure)
- Venous thrombosis limb (blood clot that forms in a vein in the limb)
- Interstitial lung disease
male:
- Febrile neutropenia (fever with reduced white blood cells)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Rash erythematous (redness of the skin)
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
What are the common drug interactions of Arixtra and Zoledronic Acid, 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:
- Interstitial lung disease
- Febrile neutropenia (fever with reduced white blood cells)
- Sepsis (a severe blood infection that can lead to organ failure and death)
- Cardio-respiratory arrest (sudden dysfunction of heart and lungs)
- Thrombocytopenia (decrease of platelets in blood)
50-59:
- Constipation
- Oedema peripheral (superficial swelling)
- Rash
- Skin discolouration (change of skin colour)
60+:
- Diarrhoea
- Dysphagia (a condition in which swallowing is difficult or painful)
- Tooth erosion (dissolving teeth)
- Vomiting
- Weight decreased
- Hypertension (high blood pressure)
- Venous thrombosis limb (blood clot that forms in a vein in the limb)
- Rash erythematous (redness of the skin)
- Lumbar spinal stenosis (a medical condition in which the spinal canal narrows and compresses the spinal cord and nerves at the level of the lumbar bone)
- Chest pain
What are the existing conditions these people have? *
- Breast Cancer: 24 people, 48.98%
- Breast Cancer Metastatic: 22 people, 44.90%
- Multiple Myeloma (cancer of the plasma cells): 10 people, 20.41%
- Pulmonary Embolism (blockage of the main artery of the lung): 7 people, 14.29%
- Squamous Cell Carcinoma (a cancer of a kind of epithelial cell): 4 people, 8.16%
* Approximation only. Some reports may have incomplete information.
Do you take Arixtra and Zoledronic acid?
- 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:
- Arixtra (9,830 reports)
- Zoledronic acid (28,485 reports)
Browse all drug interactions of Arixtra and Zoledronic acid:
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 Zoledronic acid:
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 Zoledronic acid 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 fondaparinux sodium and zoledronic acid (the active ingredients of Arixtra and Zoledronic acid, respectively), and Arixtra and Zoledronic acid (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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