نتایج جستجو برای: novoseven

تعداد نتایج: 115  

Journal: :iranian journal of pharmaceutical research 0
mina golestani school of pharmacy, shahid beheshti university of medical sciences, tehran, iran, iranian center of excellence in health management, faculty of management and medical informatics, tabriz university of medical sciences, tabriz, iran peyman eshghi pediatric hematology and oncology , pediatric congenital hematologic disorders research center, shahid beheshti university of medical sciences, tehran, iran hamid reza rasekh school of pharmacy, shahid beheshti university of medical sciences, tehran, iran abdoll majid cheraghali school of pharmacy, university of baqiyatallah medical sciences, tehran, iran jamshid salamzadeh school of pharmacy, shahid beheshti university of medical sciences, tehran,iran majid naderi genetics of non-communicable disease research center, zahedan university of medical sciences, zahedan, iran

abstract nowadays, bypassing agents such as recombinant activated factor vii (rfviia) and activated prothrombin complex concentrates (apcc) are used to treat bleeding episodes in the hemophilia patients with inhibitors. aryoseven® is an iranian biogeneric rfviia with homogeneity of efficacy and the nature to novoseven in a comparative trial. the current clinical trial aimed to evaluate the cost...

Journal: :Stroke 2005
Carlos S Kase

The treatment of intracerebral hemorrhage (ICH) has been a largely neglected item. In contrast to literally dozens of clinical trials of treatment of ischemic stroke, only a handful have addressed treatment of ICH with either medical (steroids,1 osmotic diuretics2) or surgical3 interventions. The medical intervention trials, primarily aimed at reducing brain edema surrounding the ICH, have show...

2014
Upul GP Pathirana Nirmali Gunawardena Hiranya Abeysinghe Hannah Charlotte Copley MG Dhammika Somarathne

INTRODUCTION Acquired haemophilia A is a rare life- and limb-threatening bleeding disorder if left untreated. Autoimmune thyroiditis is an autoimmune disorder that can be rarely associated with acquired haemophilia. Here we report a case of a 60-year-old woman presenting with cutaneous and muscle haematomas secondary to acquired haemophilia A in association with autoimmune thyroiditis, who was ...

Journal: :Pathophysiology of haemostasis and thrombosis 2002
Maadh Aldouri

Recombinant factor VIIa (rFVIIa, NovoSeven) is effective and appears safe in the management of bleeding episodes and provision of surgical cover in haemophilia patients with inhibitors. Additionally, rFVIIa has been considered as a universal haemostatic agent, prompting its use in the management of severe uncontrolled surgical bleeding in patients without pre-existing coagulopathies. Recombinan...

Journal: :Injury 2007
Peter Cameron Louise Phillips Zsolt Balogh Anthony Joseph Andrew Pearce Michael Parr Gary Jankelowitz

BACKGROUND There is increasing use of rFVIIa (eptagog alpha, Novoseven) in injured patients with critical bleeding. The role of rFVIIa is not defined in this group of patients. Registries provide an opportunity to review the patients, reported response and adverse events for rFVIIa. AIM To determine the pattern of use, reported response and adverse events in patients receiving rFVIIa followin...

Journal: :The Journal of trauma 2010
Carl J Hauser Kenneth Boffard Richard Dutton Gordon R Bernard Martin A Croce John B Holcomb Ari Leppaniemi Michael Parr Jean-Louis Vincent Bartholomew J Tortella Jeannett Dimsits Bertil Bouillon

BACKGROUND Traumatic coagulopathy contributes to early death by exsanguination and late death in multiple organ failure. Recombinant Factor VIIa (rFVIIa, NovoSeven) is a procoagulant that might limit bleeding and improve trauma outcomes. METHODS We performed a phase 3 randomized clinical trial evaluating efficacy and safety of rFVIIa as an adjunct to direct hemostasis in major trauma. We stud...

Journal: :Blood transfusion = Trasfusione del sangue 2015
Laura Candiotto Franco W Fullone Alberto Ricciardi Paolo Radossi Giuseppe Tagariello

Introduction Haemophilia A is a congenital bleeding disorder due to the lack of coagulation factor VIII (FVIII). The standard treatment is based on administration of plasma-derived or recombinant FVIII concentrates. The natural history of the disease includes recurrent bleeding into joints and the major long-term disability in affected patients is chronic arthropathy. The life expectancy of pat...

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