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FDA Approves Expanded Use of Lilly's FORTEO(R) [teriparatide (rDNA origin) injection] to Treat Glucocorticoid-Induced Osteoporosis
Date:7/23/2009

ate printed on the delivery device and packaging. Throw away the FORTEO delivery device after 28 days even if it has medicine in it (see the User Manual).

For more information about FORTEO, including full prescribing information, visit www.Forteo.com.

About Lilly

Lilly, a leading innovation-driven corporation, is developing a growing portfolio of pharmaceutical products by applying the latest research from its own worldwide laboratories and from collaborations with eminent scientific organizations. Headquartered in Indianapolis, Ind., Lilly provides answers -- through medicines and information -- for some of the world's most urgent medical needs. Additional information about Lilly is available at www.lilly.com.

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Forward Looking Statement

This press release contains forward-looking statements about the safety and efficacy of FORTEO and reflects Lilly's current beliefs. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of development and commercialization. There is no guarantee that FORTEO will continue to be commercially successful. For further discussion of these and other risks and uncertainties, see Lilly's filings with the United States Securities and Exchange Commission. Lilly undertakes no duty to update forward-looking statements.

(1) Trends Endocrinol. 2006; 17: 144-149.

(2) Clin Rheumatol. 2007; 26: 144-153.

(3) Endocrinol Metab Clin North Am. 2003; 32: 135-157.

(4) Van Staa, TP "The Pathogenesis, Epidemiology and Management of Glucocorticoid-Induced Osteoporosis," Calcif Tissue Int. 2006; 79:129-137.

(5) N Engl J Med. 2007; 357:2028-39.

(6) FORTEO Prescribing Information.

(7) Curr Opin Orthop.'/>"/>

SOURCE Eli Lilly and Company
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