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| Arixtra Injection® | |
| Brand Name: | Arixtra® |
| Active Ingredient: | fondaparinux sodium |
| Strength(s): | 2.5 mg/0.5 mL |
| Dosage Form(s): | Sucutaneous Injection |
| Company Name: | Fonda BV |
| Availability: | Prescription only, professional use only |
| *Date Approved by the FDA: | December 7, 2001 |
| *Approval by FDA does not mean that the drug is available for consumers at this time. | |
| What is Arixtra used for?
Arixtra is used to reduce the risk of blood clots in the veins, which may break off and travel to the lungs (pulmonary embolism) in patients undergoing:
Who should not be given Arixtra? Arixtra should not be given to people who:
Tell your health care provider if you have any of these conditions. Special Warnings with Arixtra: Arixtra and other medicines like it can cause bleeding into the spine when used in patients who have received epidural or spinal anesthesia, or any spinal injection. Bleeding in the spine can cause long term or permanent paralysis. Arixtra, like other medicines that prevent the blood from clotting, is given with extreme caution to people who have conditions that have an increased risk of bleeding, such as:
General Precautions with Arixtra: Certain other medicines can increase the risk of bleeding with Arixtra. Tell your doctor about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Especially, tell your doctor or health care provider if you are taking:
What should I tell my health care provider? Tell your health care provider if you have:
What are some possible side effects of Arixtra? (This list is NOT a complete list of side effects reported with Arixtra. Your health care provider can discuss with you a more complete list of side effects.) The most common side effect with Arixtra is bleeding. For more detailed information about Arixtra, ask your health care provider or pharmacist. |
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**This information came from an FDA consumer information site**
**This information is not updated - Check for updates at the FDA site**
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