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Azor(TM) Reduces Blood Pressure in Difficult to Treat Special Populations
Date:5/15/2008

/20 mg), 6.2% (5/40 mg), 13.3% (10/20 mg), and 11.2% (10/40 mg). The edema incidence for placebo was 12.3%.

Adverse reactions seen at lower rates but at about the same or greater incidence as in patients receiving placebo included hypotension, orthostatic hypotension, rash, pruritus, palpitation, urinary frequency, and nocturia.

In individual clinical trials of amlodipine and olmesartan medoxomil, other commonly reported adverse reactions included headache, dizziness, and flushing.

For more information on AZOR, call 877-4-DSPROD (877-437-7763) or go to the web site http://www.azor.com.

About Daiichi Sankyo, Inc.

Daiichi Sankyo, Inc., headquartered in Parsippany, New Jersey, is the U.S. subsidiary of Daiichi Sankyo Co., Ltd., Japan's second largest pharmaceutical company and a global leader in pharmaceutical innovation since 1899. The company is dedicated to the discovery, development and commercialization of innovative medicines that improve the lives of patients throughout the world. The primary focus of Daiichi Sankyo's research and development is cardiovascular disease, including therapies for dyslipidemia, hypertension, diabetes, and acute coronary syndrome. The company is also pursuing the discovery of new medicines in the areas of glucose metabolic disorders, infectious diseases, cancer, bone and joint diseases, and immune disorders.

For more information, please visit http://www.dsus.com.

* SeDBP = Seated Diastolic Blood Pressure. According to the JNC 7, a

SeDBP between 90 and 99 is considered stage 1 hypertension and 100

and above is considered stage 2 hypertension.

(1) Ong KL, et al. Prevalence, awareness, treatment and control of

hypertension among United States Adults 1999-2004. Hypertens 2007;

49: 69-75

(2) Margolis et al. Blood Pressure Control
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SOURCE Daiichi Sankyo, Inc.
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