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European Commission Approves ATRIPLA(R) (efavirenz 600 mg/emtricitabine 200 mg/tenofovir disoproxil fumarate 300 mg), the First Once-Daily Single Tablet Regimen for Virologically Suppressed Adults With HIV-1 Infection
Date:12/17/2007

ead assumes no obligation to update any such forward-looking statements.
Full U.S. prescribing information, including Boxed WARNINGS, 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, including

Boxed WARNINGS, 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 Company
Copyright©2007 PR Newswire.
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