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The present study examined whether rofecoxib (VIOXX), a new specific inhibitor Center for Biotechnology Information at the U.S. National Library of Medicine
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Merck's decision to withdraw Vioxx (rofecoxib) is based on new data from a labeling change for Vioxx in 2002 that included information about
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OBJECTIVE: To determine whether the cyclooxygenase (COX)-2 inhibitor rofecoxib increases the regression rates of cervical intraepithelial
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30, 2004 Merck & Co., Inc. announced a voluntary worldwide withdrawal of VIOXX® (rofecoxib). Please be aware that the information below is
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The FDA has approved changes to the prescribing information for rofecoxib ( Vioxx) to include results from the VIGOR study, Merck has
Home > Health Products Regulation > Safety Information and Recalls > Product Safety Alerts > 2004 > Withdrawal of rofecoxib (Vioxx®)
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Abstract: The development of a COX-2 inhibitor rofecoxib (MK 966, Vioxx~) is described. It is essentially equipotent to indomethacin both in vitro and in vivo but
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Rofecoxib withdrawn worldwide by Merck Whitehouse Station, NJ - Merck has withdrawn its selective COX-2 inhibitor rofecoxib (Vioxx®) from all markets study was conducted in part to ascertain more information on this.
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