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European CHMP Issues Positive Opinion for ATRIPLA(R) (efavirenz 600 mg/ emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg)
Date:10/18/2007

ard-looking statements in this press release should be evaluated together with the many uncertainties that affect Merck's business, particularly those mentioned in the risk factors and cautionary statements in Item 1A of Merck's Form 10-K for the year ended Dec. 31, 2006, and in its periodic reports on Form 10-Q and Form 8-K, which the Company incorporates by reference.

Full U.S. prescribing information for ATRIPLA is available at http://www.atripla.com.

Full U.S. prescribing information for SUSTIVA is available at http://www.bms.com.

Full U.S. prescribing information for Truvada, Viread and Emtriva are

available at http://www.gilead.com. EU Summary of Product Characteristics for Truvada, Viread, Emtriva, SUSTIVA

and Stocrin are available at

http://www.emea.europa.eu/htms/human/epar/a.htm. ATRIPLA is a registered trademark of Bristol-Myers Squibb & Gilead Sciences,

LLC. SUSTIVA is a registered trademark of Bristol-Myers Squibb Pharma Company.

Stocrin is a registered trademark of Merck & Co., Inc. Truvada, Viread and Emtriva are all registered trademarks of Gilead Sciences,

Inc.


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SOURCE Bristol-Myers Squibb
Copyright©2007 PR Newswire.
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