Literature DB >> 27799968

Evaluation of Aryoseven Safety (Recombinant Activated Factor VII) in Patients with Bleeding Disorders (An Observational Post-Marketing Surveillance Study).

Gholamreza Toogeh1, Hassan Abolghasemi2, Peyman Eshghi2, Mohammadreza Managhchi1, Mohammadreza Shaverdi-Niasari1, Katayoon Karimi1, Samin Roostaei1, Neda Emran1, Alireza Abdollahi3.   

Abstract

BACKGROUND: Recombinant activated factor VII induces hemostasis in patients with coagulopathy disorders. AryoSeven™ as a safe Iranian Recombinant activated factor VII has been available on our market. This study was performed to establish the safety of AryoSeven on patients with coagulopathy disorder.
METHODS: This single-center, descriptive, cross sectional study was carried out in Thrombus and Homeostasis Research Center ValiAsr Hospital during 2013-2014. Fifty one patients with bleeding disorders who received at least one dose of Aryoseven were enrolled. Patients' demographic data and adverse effect of drug and reaction related to Aryoseven or previous usage of Recombinant activated FVII were recorded in questionnaires. Finally data were analyzed to compare side effects of Aryoseven and other Recombinant activated FVII brands.
RESULTS: Aryoseven was prescribed for 51 Patients. Of all participants with mean age 57.18+21.38 yr, 31 cases were male and 26 subjects had past history of recombinant activated FVII usage. Glanzman was the most frequent disorder followed by congenital FVII deficiency, hemophilia with inhibitors, factor 5 deficiency, acquired hemophilia, hemophilia A with inhibitor, and hemophilia A or B with inhibitor. The majority of bleeding episodes had occurred in joints. Three patients (5.9%) complained about adverse effects of Aryoseven vs. 11.5 % about adverse effects of other brands. However this difference was not significant, statistically.
CONCLUSION: Based on monitor patients closely for any adverse events, we concluded that Aryoseven administration under careful weighing of benefit versus potential harm may comparable with other counterpart drugs.

Entities:  

Keywords:  Aryoseven; Bleeding disorders; Safety

Year:  2016        PMID: 27799968      PMCID: PMC5079452     

Source DB:  PubMed          Journal:  Iran J Pathol        ISSN: 1735-5303


  19 in total

1.  A modeling approach to evaluate long-term outcome of prophylactic and on demand treatment strategies for severe hemophilia A.

Authors:  Kathelijn Fischer; Maurice E Pouw; Daniel Lewandowski; Mart P Janssen; H Marijke van den Berg; Ben A van Hout
Journal:  Haematologica       Date:  2011-01-27       Impact factor: 9.941

2.  Home treatment of mild to moderate bleeding episodes using recombinant factor VIIa (Novoseven) in haemophiliacs with inhibitors.

Authors:  N S Key; L M Aledort; D Beardsley; H A Cooper; G Davignon; B M Ewenstein; G S Gilchrist; J C Gill; B Glader; W K Hoots; C T Kisker; J M Lusher; C G Rosenfield; A D Shapiro; H Smith; E Taft
Journal:  Thromb Haemost       Date:  1998-12       Impact factor: 5.249

3.  Implementation of an off-label recombinant factor VIIa protocol for patients with critical bleeding at an academic medical center.

Authors:  Jonathan Bain; Daniel Lewis; Andrew Bernard; Kevin Hatton; Hassan Reda; Jeremy Flynn
Journal:  J Thromb Thrombolysis       Date:  2014-11       Impact factor: 2.300

4.  Dosing and effectiveness of recombinant activated factor VII (rFVIIA) in congenital haemophilia with inhibitors by bleed type and location: the experience of the Haemophilia and Thrombosis Research Society (HTRS) Registry (2004-2008).

Authors:  G Young; D L Cooper; R Z Gut
Journal:  Haemophilia       Date:  2012-05-28       Impact factor: 4.287

Review 5.  The use of recombinant factor VIIa (NovoSeven) for treatment of active or impending bleeding in brain injury: broadening the indications.

Authors:  Yakov Yusim; Azriel Perel; Haim Berkenstadt; Moshe Attia; Nachshon Knoller; Avner Sidi
Journal:  J Clin Anesth       Date:  2006-11       Impact factor: 9.452

Review 6.  Safety update on the use of recombinant factor VIIa and the treatment of congenital and acquired deficiency of factor VIII or IX with inhibitors.

Authors:  T Abshire; G Kenet
Journal:  Haemophilia       Date:  2008-08-04       Impact factor: 4.287

7.  Incidence of development of factor VIII and factor IX inhibitors in haemophiliacs.

Authors:  S Ehrenforth; W Kreuz; I Scharrer; R Linde; M Funk; T Güngör; B Krackhardt; B Kornhuber
Journal:  Lancet       Date:  1992-03-07       Impact factor: 79.321

8.  Pharmacodynamics of recombinant activated factor VII and plasma-derived factor VII in a cohort of severe FVII deficient patients.

Authors:  Mark van Geffen; Natascha C J Mathijssen; Pål A Holme; Britta A P Laros-van Gorkom; Marian G J van Kraaij; Roselinde Masereeuw; Flora Peyvandi; Waander L van Heerde
Journal:  Thromb Res       Date:  2013-05-31       Impact factor: 3.944

Review 9.  Recombinant factor VIIa (NovoSeven) as a hemostatic agent.

Authors:  Ulla Hedner
Journal:  Dis Mon       Date:  2003-01       Impact factor: 3.800

10.  The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99.

Authors:  S C Darby; D M Keeling; R J D Spooner; S Wan Kan; P L F Giangrande; P W Collins; F G H Hill; C R M Hay
Journal:  J Thromb Haemost       Date:  2004-07       Impact factor: 5.824

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  1 in total

1.  Comparative evaluation of the safety and efficacy of recombinant FVIII in severe hemophilia A patients.

Authors:  Hassan Abolghasemi; Yunes Panahi; Minoo Ahmadinejad; Gholamreza Toogeh; Mehran Karimi; Aziz Eghbali; Nargess Bigom Mirbehbahani; Bighan Keikhaei Dehdezi; Zahra Badiee; Hamid Hoorfar; Peyman Eshghi; Nader Maghsoudi; Amirhossein Sahebkar; Mohammad Gholami-Fesharaki
Journal:  J Pharmacopuncture       Date:  2018-06-30
  1 in total

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