GSK has halted all shipments of ARIXTRA Starter Kits containing the Triad For important product information, log onto Arixtra mg/ ml solution for injection, pre-filled syringe. 2. .. Detailed information on this medicinal product is available on the website of the European . Arixtra is a medicine that helps prevent blood clots from forming in the blood This medicinal product contains less than 23 mg of sodium in each dose and.

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No dosage adjustment required in patients with mild to moderate hepatic impairment. Epidural or spinal hematoma reported with concurrent use of anticoagulants e. Discontinue platelet-aggregation inhibitors prior to initiation of fondaparinux 1 40 If coadministration is essential, monitor patients closely 1 If coadministration prscribing essential, monitor patients closely 1 A new synthetic pentasaccharide for thrombosis prevention.

Lovenox arixtar sodium injection prescribing information. A randomized double-blind comparison. Insert the entire length of the needle into a skin fold created by the thumb and forefinger; hold the skin fold, and push the plunger of the syringe the full length of the syringe barrel.

Amended economic impact analysis of final rule requiring use of labeling on natural rubber containing devices. Used in conjunction with warfarin for treatment of DVT and acute Infornation when initial therapy is administered in the hospital. Postoperative wound infection, postoperative hemorrhage, fever, surgical site reaction, anemia, hypertension, pneumonia, vomiting.


Duration of prophylaxis against venous thromboembolism with fondaparinux after hip fracture surgery: Prevention of VTE in nonsurgical patients: Efficacy and safety of fondaparinux versus enoxaparin in patients with informatio coronary syndromes undergoing percutaneous coronary intervention: This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment.

Bounameaux, H, Perneger T.

Prevention of VTE in orthopedic surgery patients: Natural rubber-containing medical devices; user labeling. Dosages for fondaparinux sodium and heparin, heparinoids, or LMWHs cannot be used interchangeably on a unit-for-unit or mg-for-mg basis 1 as they differ in the manufacturing process, anti-factor Xa and antithrombin activity, and dosage. ACCP recommends fondaparinux as an option for thromboprophylaxis in acutely ill, hospitalized medical patients at increased risk of thrombosis.

Usual duration of therapy is 5—9 days, although up to 10 days has been studied. In healthy adults, distributes mainly in blood and only to a minor extent in extravascular fluid.

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Prevention of postoperative DVT and PE in patients undergoing hip-fracture, hip-replacement, predcribing knee-replacement surgery. Eliminated unchanged in urine in individuals with normal renal function. Do not administer earlier than 6—8 hours after surgery because of increased risk of major bleeding. Hull R, Pineo G. In general, pharmacologic thromboprophylaxis is recommended only in such patients considered to be at high risk of venous thromboembolism.


A randomized double-blind trial.

Arixtra Monograph for Professionals –

Importance of patients informing clinicians including dentists that they are receiving fondaparinux therapy before scheduling any invasive procedures. Used for extended prophylaxis i. Some packaging components e. Fondaparinux or enoxaparin for the initial treatment of symptomatic deep venous thrombosis: N Engl J Med.

Clin Appl Thromb Hemost. Importance of informing patients that presscribing use of aspirin or other NSAIAs can increase risk of bleeding, and to discontinue use of these drugs whenever possible. Bridgewater, NJ; Jul. Increased risk of hemorrhage; closely monitor for signs and symptoms of bleeding. The activity of fondaparinux sodium is measured based on plasma drug concentrations quantified by anti-factor Xa activity using fondaparinux as the calibrator. Postoperative fondaparinux inforkation preoperative enoxaparin for prevention of venous thromboembolism in elective hip-replacement surgery: