Fondaparinux Sodium
- 1 January 2002
- journal article
- review article
- Published by Springer Nature in Drugs
- Vol. 62 (11) , 1673-1685
- https://doi.org/10.2165/00003495-200262110-00007
Abstract
▴ Fondaparinux sodium, a selective factor Xa inhibitor, is the first in a new class of antithrombotics. It binds selectively with high affinity to antithrombin III and specifically catalyses the inactivation of factor Xa. The elimination half-life of fondaparinux sodium permits once daily treatment. ▴ A randomised, double-blind, parallel-group, dose-ranging, multicentre phase IIb study in 933 eligible patients established that a subcutaneous dose of between 1.5 and 3mg of fondaparinux sodium has the optimum efficacy and safety profile for prophylaxis of venous thromboembolism in patients undergoing major orthopaedic surgery. ▴ Fondaparinux sodium, given to more than 3600 patients undergoing major orthopaedic surgery who participated in prospective, randomised, double-blind, multicentre phase III clinical trials, significantly reduced the incidence of venous thromboembolism, with an overall risk reduction of 55.2% compared with enoxaparin. ▴ Fondaparinux sodium was well tolerated by patients undergoing major orthopaedic surgery, and at the recommended clinical dose of 2.5mg has a similar tolerability profile, including bleeding events, to standard enoxaparin regimens. Fondaparinux sodium has not been reported to cause antibody-induced thrombocytopenia.Keywords
This publication has 46 references indexed in Scilit:
- Choosing a Parenteral Anticoagulant AgentNew England Journal of Medicine, 2001
- A Synthetic Pentasaccharide for the Prevention of Deep-Vein ThrombosisNew England Journal of Medicine, 2001
- Redesigning HeparinNew England Journal of Medicine, 2001
- Recent advances in clinical trials of the direct and indirect selective Factor Xa inhibitorsExpert Opinion on Investigational Drugs, 2000
- Low-Molecular-Weight HeparinsNew England Journal of Medicine, 1997
- Synthesis and Pharmacological Properties of a Close Analogue of an Antithrombotic Pentasaccharide (SR 90107A/ORG 31540)Journal of Medicinal Chemistry, 1997
- Absence of cross-reactivity of SR90107A/ORG31540 pentasaccharide with antibodies to heparin-PF4 complexes developed in heparin-induced thrombocytopeniaBlood Coagulation & Fibrinolysis, 1997
- SR 90107A/Org 31540, a Novel Anti‐Factor Xa Antithrombotic AgentCardiovascular Drug Reviews, 1997
- New Antithrombotic Agents For The Prevention And Treatment Of Deep Vein ThrombosisPathophysiology of Haemostasis and Thrombosis, 1996
- Venous Thromboembolism Associated With Hip and Knee Arthroplasty: Current Prophylactic Practices and OutcomesMayo Clinic Proceedings, 1992