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FDA Approves Cymbalta® for the Management of Chronic Musculoskeletal Pain
Date:11/4/2010

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.

This press release contains forward-looking statements about the potential of Cymbalta for the management of chronic musculoskeletal pain, 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 the product 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.

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(i) Lawrence RC, et al. Arthr Rheum. 2008.58(1):26-35.

(ii) Andersson GBJ. Lancet. 1999;354:581-585.

(iii) Burton AK et al. European Guidelines for Prevention of Low Back Pain. www.backpaineurope.org.  2004:1-53.

(iv) Freburger JK, et al. Arch Int Med. 2009; 169(3):251-258.

(v) Klenerman L, et al. Spine. 1995; 20(4):478-484.

(vi) Van Den Hoogen HJM, et al. Ann Rheum Dis. 1998; 57:13-19.

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