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FDA Advisory Committee Recommends Approval of KYNAPID(TM) for Acute Atrial Fibrillation
Date:12/11/2007

ing statements and information made herein are based on our current expectations and we undertake no obligation to revise or update such forward-looking statements and information to reflect subsequent events or circumstances, except as required by law.

CONTACT: Peter K. Hofman, Senior Director, Investor Relations, Cardiome Pharma Corp., (604) 676-6993 or Toll Free: 1-800-330-9928, Email: phofman@cardiome.com; Maribeth Landwehr, Astellas US LLC, (847) 317-8988; Ulysee Huling For Astellas Pharma US, Inc., (312) 397-6614


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SOURCE Cardiome Pharma Corp.
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