Arixtra and Methylprednisolone drug interactions - a phase IV clinical study of FDA data
Summary:
Drug interactions are reported among 44 people who take Arixtra and Methylprednisolone. Common interactions include skin exfoliation among females, and sepsis among males.
The phase IV clinical study analyzes what interactions people who take Arixtra and Methylprednisolone have. It is created by eHealthMe based on reports from the FDA, and is updated regularly. You may use the study as a second opinion to make health care decisions.
Phase IV trials are used to detect adverse drug outcomes and monitor drug effectiveness in the real world. With medical big data and AI algorithms, eHealthMe is running millions of phase IV trials and makes the results available to the public. Our original studies have been referenced on 700+ medical publications including The Lancet, Mayo Clinic Proceedings, and Nature.
44 people who take Arixtra and Methylprednisolone together, and have interactions are studied.
What is Arixtra?
Arixtra has active ingredients of fondaparinux sodium. It is used in deep venous thrombosis. Currently, eHealthMe is studying from 9,694 Arixtra users.
What is Methylprednisolone?
Methylprednisolone has active ingredients of methylprednisolone. It is used in inflammation. Currently, eHealthMe is studying from 49,469 Methylprednisolone users.
Number of Arixtra and Methylprednisolone reports submitted per year:

Common Arixtra and Methylprednisolone drug interactions by gender *:
female:
- Skin exfoliation
- Thrombophlebitis superficial
- Thrombosis
- Colitis
- Diarrhoea
- Vascular occlusion
- Pancytopenia
- Cerebral haemorrhage
- Respiratory failure
- Large intestinal haemorrhage
male:
- Sepsis
- Rash erythematous
- Disease progression
- Fluid retention
- Ileus paralytic
- Large intestinal haemorrhage
- Neoplasm malignant
- Pancytopenia
- Paresis
- Sensory loss
Common Arixtra and Methylprednisolone drug interactions by age *:
0-1:
n/a
2-9:
n/a
10-19:
n/a
20-29:
n/a
30-39:
n/a
40-49:
- Febrile bone marrow aplasia
- Haematoma
- Pelvic venous thrombosis
- Pulmonary embolism
- Purpura
- Thrombocytopenia
- Thrombophlebitis superficial
50-59:
- Diarrhoea
- Colitis
- Vascular occlusion
- Large intestinal haemorrhage
- Sensory loss
- Pancytopenia
- Neoplasm malignant
- Vomiting
- Disease progression
- Paresis
60+:
- Sepsis
- Haematoma
- Encephalopathy
- Haemoglobin decreased
- Neutropenia
- Platelet count decreased
- Systemic candida
- Urinary tract disorder
- Anaemia
- Anticoagulation drug level below therapeutic
Common conditions people have *:
- Peripheral Arterial Occlusive Disease (reproducible ischemic muscle pain): 8 people, 18.18%
- Malignant Melanoma (skin cancer rises from melancytes): 8 people, 18.18%
- Diarrhea: 8 people, 18.18%
- Pain: 7 people, 15.91%
- Squamous Cell Carcinoma (a cancer of a kind of epithelial cell): 4 people, 9.09%
- Progressive Multiple Sclerosis (chronic autoimmune disease of the central nervous system in which gradual destruction of myelin occurs in patches throughout the brain or spinal cord): 4 people, 9.09%
- Stable Angina (a constant chest pain): 3 people, 6.82%
- Epstein-Barr Virus Infection: 3 people, 6.82%
- Epilepsy (common and diverse set of chronic neurological disorders characterized by seizures): 3 people, 6.82%
* Approximation only. Some reports may have incomplete information.
Do you take Arixtra and Methylprednisolone?
Personalize this study to your gender and ageHow to use the study?
You can discuss the study with your doctor, to ensure that all drug risks and benefits are fully discussed and understood.
Related studies
Drug side effects by duration, gender and age:
- Arixtra side effects (9,694 reports)
- Methylprednisolone side effects (49,469 reports)
Common Arixtra drug interactions:
- Arixtra and Aspirin: 544 reports
- Arixtra and Lasix: 517 reports
- Arixtra and Nexium: 455 reports
- Arixtra and Lovenox: 396 reports
- Arixtra and Pantoprazole: 378 reports
- Arixtra and Furosemide: 358 reports
- Arixtra and Plavix: 356 reports
- Arixtra and Omeprazole: 317 reports
- Arixtra and Coumadin: 298 reports
- Arixtra and Morphine: 284 reports
Browse 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 zCommon Methylprednisolone drug interactions:
- Methylprednisolone and Prednisone: 9,861 reports
- Methylprednisolone and Acetaminophen: 9,717 reports
- Methylprednisolone and Diphen: 6,976 reports
- Methylprednisolone and Hydramine: 6,972 reports
- Methylprednisolone and Methotrexate: 6,897 reports
- Methylprednisolone and Mycophenolate mofetil: 5,286 reports
- Methylprednisolone and Prednisolone: 5,137 reports
- Methylprednisolone and Tacrolimus: 4,757 reports
- Methylprednisolone and Cyclosporine: 4,112 reports
- Methylprednisolone and Pantoprazole: 3,362 reports
Browse interactions between Methylprednisolone 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 methylprednisolone (the active ingredients of Arixtra and Methylprednisolone, respectively), and Arixtra and Methylprednisolone (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. Patients in the study may take other drugs besides Arixtra and Methylprednisolone.
Who is eHealthMe?
With medical big data and proven AI 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 700+ 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
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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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