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 |