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Cadence Pharmaceuticals Reaffirms FDA-Approved Dosing Recommendations for OFIRMEV® (acetaminophen) Injection
Date:7/28/2011

>Forward-Looking Statements Statements included in this press release that are not a description of historical facts are forward-looking statements. Words such as "plans," "believes," "expects," "anticipates," and "will," and similar expressions, are intended to identify forward-looking statements, and are based on Cadence's current beliefs and expectations. Actual results could differ materially from those stated or implied by these forward-looking statements due to risks associated with Cadence's business.  Such risks are detailed under "Risk Factors" and elsewhere in Cadence's periodic reports and other filings made with the Securities and Exchange Commission from time to time. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of Section 21E of the Private Securities Litigation Reform Act of 1995, and Cadence undertakes no obligation to revise or update this press release to reflect events or circumstances after the date hereof.

Cadence® and OFIRMEV® are trademarks of Cadence Pharmaceuticals, Inc. Contact:

INVESTORS

MEDIACadence Pharmaceuticals, Inc.

WCGWilliam R. LaRue

Kelli FranceSVP & Chief Financial Officer

Media RelationsPhone: (858) 436-1400

Phone: (415) 946-1076blarue@cadencepharam.com

kfrance@wcgworld.com
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SOURCE Cadence Pharmaceuticals, Inc.
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