Takeda Pharmaceuticals Rebecca - In the 21st century there are hundreds of pharmaceutical companies in operation around the world. In this article, we spend some time considering Takeda Pharmaceuticals Rebecca Smith reviews.
Keep in mind that nothing in this article should be construed as being an endorsement of Takeda Pharmaceuticals. Rather, the information contained in this article is only a Takeda Pharmaceuticals Rebecca Smith review.
We merely provide the Takeda Pharmaceuticals Rebecca Smith for informational purposes. If a person desires information in addition to the Takeda Pharmaceuticals Rebecca Smith, we strongly suggest that a person spend some time doing an independent investigation of the company.
Rebecca Smith reports: “since our inception, TPNA has focused on being a good corporate citizen to the communities where our employees and patients live and work. Our philanthropic mission is to help improve the lives of the people in the communities we serve. Find out more about our dedication to helping others.”
Rebecca Smith further updates people on the current work of the company noting: “in addition to marketing ACTOS (pioglitazone HCl), and co-promoting Niaspan® (niacin extended-release tablets) and Advicor (niacin extended-release/lovastatin tablets), TPNA has a promising, early-stage pipeline. Learn more about TPNA’s products and compounds in development.”
The company provides more detailed information on ACTOS: “takeda Pharmaceuticals North America, Inc. currently markets the oral diabetes treatment ACTOS® (pioglitazone HCl) in the United States. Since its U.S. launch in 1999, more than 30 million prescriptions for ACTOS have been written.
ACTOS is an insulin sensitizer for people with type 2 diabetes. ACTOS is a member of the class of oral diabetes agents called thiazolidinediones (THIGH-ah-ZO-li-deen-DYE-owns, TZDs). Scientists at TPNA’s parent company, Takeda Pharmaceutical Company Limited, were leaders in the discovery of the TZD molecule and have been instrumental in advancing the class. The U.S. Food and Drug Administration approved ACTOS in July 1999. In September 2002, ACTOS became the number one prescribed TZD in the United States. In April 2003, TPNA announced the initiation of two significant trials to investigate the effect of ACTOS on reducing the risk for cardiovascular disease in patients with type 2 diabetes.
Takeda Pharmaceuticals North America, Inc. co-promotes ACTOS with Eli Lilly and Company.”
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