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Data Suggest Cymbalta Improved Functioning in Patients with,Generalized Anxiety Disorder

Cymbalta is approved only for adults 18 and over.

Cymbalta is not for everyone. Patients should not take Cymbalta if they have recently taken a type of antidepressant called a monoamine oxidase inhibitor (MAOI), are taking Mellaril(R) (thioridazine) or have uncontrolled glaucoma. Patients should speak with their doctor about all medicines they are taking, including those for migraine to avoid a potentially life- threatening condition. Patients should tell their doctor about their alcohol consumption, if they have liver disease, and about all of their medical conditions.

Patients taking Cymbalta may experience dizziness or fainting upon standing. The most common side effects of Cymbalta include:

    --  For MDD: nausea, dry mouth and constipation

    --  For DPNP: nausea, sleepiness and dizziness

    --  For GAD: nausea, fatigue and dry mouth

    This is not a complete list of side effects.

For full Patient Information, visit www.cymbalta.com.

For full Prescribing Information, including Boxed Warning, visit http://www.cymbalta.com/.

About Eli Lilly and Company

Lilly, a leading innovation-driven corporation, is developing a growing portfolio of first-in-class and best-in-class 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.

P-LLY

This press release contains forward-looking statements about the potential of Cymbalta for the treatment of generalized anxiety disorder, and reflects Lilly's current beliefs. However, as wi
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(Date:12/1/2008)...ewswire-FirstCall/ -- Vanda Pharmaceuticals Inc. (...t , one of the world,s leading medical journals, r...egulator, experimental compound tasimelteon (VEC-1...titled "Melatonin agonist tasimelteon (VEC-162) fo...andomised controlled multicentre trials." Results ...
(Date:12/1/2008)...swire/ -- Roche announced today that a,comparativ...ived pain and,discomfort associated with blood gl...toring systems and lancing devices were deemed lea...ll, the ACCU-CHEK Aviva and ACCU-CHEK Compact,Plu...EK Multiclix, ACCU-CHEK,Softclix and ACCU-CHEK So...
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(Date:12/1/2008)...d for Tuesday, December 9 at 11:00 am ET to Discus...H SAN FRANCISCO, Calif., Dec. 1 /PRNewswire-Firs... SNSS ), a biopharmaceutical company focused on th...y therapeutics, today announced new data from its ...L) will be presented during the 50th American Soci...
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...ducts are offered as 1-piece or modular, in regula...ay be customized with handles of choice and other ...ts. Many standard patterns are available from Medi...ivery times. , Please Note: Individual instrumen...
...ducts are offered as 1-piece or modular, in regula...ay be customized with handles of choice and other ...ts. Many standard patterns are available from Medi...ivery times. , Please Note: Individual instrumen...
...ducts are offered as 1-piece or modular, in regula...ay be customized with handles of choice and other ...ts. Many standard patterns are available from Medi...ivery times. , Please Note: Individual instrumen...
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