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Table 1 Treatment of Acute Hereditary Angioedema - HAE - Attacks - 2010 XII 21

From: Hereditary angioedema: beyond international consensus - circa December 2010 - The Canadian Society of Allergy and Clinical Immunology Dr. David McCourtie Lecture

ANGIOEDEMA EVENT THERAPIES (AERx's)

TREAT AS EARLY AS POSSIBLE IN AN ATTACK

Plasma-derived C1 INH (pdC1INH) (intravenous)

○ Berinert® CSL Behring - approved in many countries (including Europe and North America)

 

   ▪ 20 units/kg intravenously (FDA licensed dose)

 

○ Cetor® Sanquin - approved in the Netherlands 1997

 

   ▪ 1000 units intravenously

 

○ Cinryze® ViroPharma - under review for therapy

Recombinant C1INH (rhC1INH) (intravenous)

○ conestat alfa, Rhucin® non-European and Ruconest® in Europe; Pharming

 

   ▪ 50 units/kg intravenously

 

â—‹ approved for use by the European Medicines Agency (EMA) for use in the European Union 2010

 

â—‹ under review in North America

Bradykinin B2 receptor antagonist (subcutaneous)

○ Icatibant - 30 mg (subcutaneous) (Firazyr® (Jerini/Shire)

 

â—‹ approved for use by the European Medicines Agency (EMA) for use in the European Union 2008

 

â—‹ not yet approved in North America

Kallikrein receptor antagonist (subcutaneous)

○ Ecallantide, Dyax, DX-88, Kalbitor®

 

â—‹ 30 mg subcutaneously

 

â—‹ approved USA 2009 - not yet available in Canada

  1. *Modified from: www.haecanada.com and 2010 International Consensus Algorithm for the Diagnosis, Therapy and Management of Hereditary Angioedema - Bowen et al. Allergy, Asthma & Clinical Immunology 2010, 6 :24 - http://www.aacijournal.com/content/6/1/24)