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ViroPharma Incorporated Reports Third Quarter 2008 Financial Results
Date:10/29/2008

our ability to file an initial NDA, MAA and NDS for maribavir in 2009, the timing and content of final IDSA/SHEA CDI treatment guidelines, the effectiveness of our Vancocin sales efforts, our estimates of future tax rates, or our ability to execute a successful launch of Cinryze later this year. ViroPharma's 2008 revenue guidance is based upon the Company's plans to remain vigorous in its opposition to any bioequivalence approach considered for use in approving generic formulations of Vancocin that does not require rigorous scientific methods to demonstrate safety and efficacy consistent with good medicine and science. There can be no assurance that the FDA will agree with the positions stated in ViroPharma's Vancocin related submissions or that ViroPharma's efforts to oppose the OGD's March 2006 recommendation to determine bioequivalence to Vancocin through in vitro dissolution testing will be successful. We cannot predict the timeframe in which the FDA will make a decision regarding either ViroPharma's citizen petition for Vancocin or the approval of generic versions of Vancocin. If we are unable to change the recommendation set forth by the OGD in March 2006, the threat of generic competition will be high. The entry of competing generic products will significantly affect our sales of Vancocin and our financial performance.

The company's actual results may vary depending on a variety of factors, including:

-- the development of competitive generic versions of oral Vancocin;

-- our ability to successfully commercialize Cinryze;

-- the availability of third party payer reimbursement for Cinryze

patients;

-- approval of products which are currently marketed for other indications

by other companies or new pharmaceuticals and technological advances to

treat the conditions addressed by Vancocin or Cinryze;

-- fluctuations in wholesaler order patterns and inventory levels;

-- manufacturing, s
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SOURCE ViroPharma Incorporated
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