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Arthritis Advisory Committee Recommends FDA Approval of Febuxostat for the Treatment of Hyperuricemia in Patients With Gout
Takeda Pharmaceutical Company Limited and its wholly-owned subsidiary, Takeda Global Research & Development Center, Inc., U.S., announced today that the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) recommended that the FDA approve febuxostat for the treatment of hyperuricemia in patients with gout.
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American Indian Tribes Hope For Improvements In IHS With Tom Daschle As HHS Secretary
American Indian tribal leaders are anticipating that former Senate Majority Leader Tom Daschle (D-S.D.) could make significant improvements to Indian Health Services to address funding shortages, health disparities and access to care if he is confirmed as HHS secretary, the More: continued here
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Mylan receives FDA approval for Fluoxetine capsules
Mylan Inc. has announced that its subsidiary, Mylan Pharmaceuticals Inc., received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Fluoxetine Capsules USP, 10 mg and 20 mg.
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Immunology in india: an emerging story
Immunology in India: an emerging story Nature Immunology 9, 1319 (2008). doi:10.1038/ni1208-1319 Author: Kanury V S Rao Although immunological research is of only recent origin in India, it is nevertheless rapidly becoming an area of choice for young researchers in this country. (Source: Nature Immunology)
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CNSystems Medizintechnik AG Receives FDA Approval For CNAP? Blood Pressure Monitor 500
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New Epilepsy Treatment Receives FDA Approval
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