Food and Drug Administration (FDA) Medical Officer Robert Sh

UNITED STATES - APRIL 12: Food and Drug Administration (FDA) Medical Officer Robert Shibuya speaks about Merck & Co.'s experimental arthritis drug Arcoxia, at a Food and Drug Administration (FDA) Arthritis Advisory Committee Meeting, in Gaithersburg, Maryland, April 12, 2007. Arthritis Advisory Committee Center For Drug Evaluation and Research Members John C. Davis, of University of California, San Francisco, right, and Christy Sandborg, of Stanford University School of Medicine, left, listen. Arcoxia would be a ``a potential public health disaster'' if approved, said a U.S. regulator long critical of Vioxx, a predecessor that was withdrawn because of dangerous side effects. (Photo by Stephanie Kuykendal/Bloomberg via Getty Images)
UNITED STATES - APRIL 12: Food and Drug Administration (FDA) Medical Officer Robert Shibuya speaks about Merck & Co.'s experimental arthritis drug Arcoxia, at a Food and Drug Administration (FDA) Arthritis Advisory Committee Meeting, in Gaithersburg, Maryland, April 12, 2007. Arthritis Advisory Committee Center For Drug Evaluation and Research Members John C. Davis, of University of California, San Francisco, right, and Christy Sandborg, of Stanford University School of Medicine, left, listen. Arcoxia would be a ``a potential public health disaster'' if approved, said a U.S. regulator long critical of Vioxx, a predecessor that was withdrawn because of dangerous side effects. (Photo by Stephanie Kuykendal/Bloomberg via Getty Images)
Food and Drug Administration (FDA) Medical Officer Robert Sh
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12 April, 2007
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