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fondaparinux sodium |
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fondaparinux sodium Arixtra Pharmacologic class: Selective factor Xa inhibitor Therapeutic class: Anticoagulant, antithrombotic Pregnancy risk category B FDA Boxed Warning• During epidural or spinal anesthesia or puncture, patients receiving drug or scheduled to receive it for thromboprophylaxis are at risk for epidural or spinal hematoma, which can lead to long-term or permanent paralysis. Risk increases with use of indwelling epidural catheter for analgesia administration and with concurrent use of drugs affecting hemostasis (such as nonsteroidal anti-inflammatory drugs, platelet inhibitors, and other anticoagulants). Risk also rises with traumatic or repeated epidural or spinal puncture. Before neuraxial intervention, physician should weigh drug's potential benefit against risk. ActionSelectively inhibits factor Xa, disrupting blood coagulation and inhibiting thrombin formation and thrombus development AvailabilityInjection: 2.5 mg/0.5 ml in single-dose syringe ⊘Indications and dosages ➣ Prevention of deep-vein thrombosis after hip fracture surgery or hip or knee replacement surgery Adults: 2.5 mg subcutaneously 6 to 8 hours after surgery, once hemostasis occurs; usual duration is 5 to 9 days (up to 11 days) given daily. After hip fracture surgery, extended prophylactic course of up to 24 additional days is recommended; some patients have tolerated a total course of 32 days. ➣ Deep-vein thrombosis and pulmonary emboli Adults: 5 mg subcutaneously once daily for patients weighing less than 50 kg (110 lb), 7.5 mg subcutaneously for patients weighing 50 to 100 kg (110 to 220 lb) or 10 mg subcutaneously for patients weighing more than 100 kg (220 lb) for 5 days and until therapeutic oral anticoagulant effect occurs (as shown by International Normalized Ratio of 2 to 3). Usual duration of therapy is 5 to 9 days, but may continue for up to 26 days. Dosage adjustment• Renal impairment Contraindications• Hypersensitivity to drug PrecautionsUse cautiously in: Administration☞ Withhold for at least 6 to 8 hours after surgery, to minimize risk of major bleeding.
Adverse reactionsCNS: depression, dizziness, asthenia, headache, abnormal thinking, confusion, insomnia, neuropathy CV: hypotension GI: nausea, vomiting, diarrhea, constipation, abdominal pain, dyspepsia, dry mouth, anorexia GU: urinary retention, urinary tract infection Hematologic: anemia, hematoma, purpura, minor bleeding, major bleeding, thrombocytopenia, retroperitoneal hemorrhage, postoperative hemorrhage Metabolic: hypokalemia Skin: bullous eruption Other: increased wound drainage, injection site bleeding, pain, edema, fever InteractionsDrug-drug. Anticoagulants: increased risk of bleeding Drug-herbs. Anise, astragalus, bilberry, black currant, bladder wrack, bogbean, boldo, borage, buchu, capsaicin, cat's claw, celery, chaparral, cinchona, clove oil, dandelion, dong quai, fenugreek, feverfew, garlic, ginger, ginkgo, papaya, red clover, rhubarb, safflower oil, skullcap, tan-shen: additive anticoagulant effect St. John's wort: reduced anticoagulant effect Patient monitoring• Monitor CBC, platelet count, creatinine level, and renal function tests. Assess stools for occult blood. Patient teaching☞ Instruct patient to immediately report bleeding. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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| The New Drug Application for fondaparinux sodium, the active compound in Arixtra, was submitted on February 15, 2001 in both the United States and Europe. |
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