EUHASS: The European haemophilia safety surveillance system

M. Makris, G. Calizzani, K. Fischer, E. A. Gilman, C. R M Hay, R. Lassila, T. Lambert, C. A. Ludlam, P. M. Mannucci

Research output: Contribution to journalArticlepeer-review

Abstract

Pharmacovigilance is an essential element of any drug treatment and considering the history of adverse events due to products used to treat inherited bleeding disorders, it should be an integral component of modern haemophilia treatment. Because inherited bleeding disorders and adverse events are rare, a multicentre, preferably multinational, adverse event reporting scheme for all clotting factor products is required. EUHASS is a European, prospective, multicentre adverse event reporting scheme in the field of inherited bleeding disorders.

Original languageEnglish
JournalThrombosis Research
Volume127
Issue numberSUPPL. 2
DOIs
Publication statusPublished - Jan 2011

Keywords

  • Adverse events
  • Haemophilia
  • Inhibitor
  • Thrombosis

ASJC Scopus subject areas

  • Hematology

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