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Volumn 357, Issue 7, 2007, Pages 633-635

Keeping science on top in drug evaluation

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOOXYGENASE 2 INHIBITOR; DEXFENFLURAMINE; ETORICOXIB; NAPROXEN; NONSTEROID ANTIINFLAMMATORY AGENT; RIMONABANT; ROFECOXIB; ROSIGLITAZONE; TROGLITAZONE;

EID: 34547958547     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMp078134     Document Type: Article
Times cited : (22)

References (5)
  • 1
    • 15744396650 scopus 로고    scopus 로고
    • 10 Voters on panel backing pain pills had industry ties
    • February 25
    • Harris G, Berenson A. 10 Voters on panel backing pain pills had industry ties. New York Times. February 25, 2005:A1.
    • (2005) New York Times
    • Harris, G.1    Berenson, A.2
  • 2
    • 85030510032 scopus 로고    scopus 로고
    • Wood S. Reauthorizing the Prescription Drug User Fee Act: how are PDUFA, the FDA budget, and drug safety related? Washington, DC: George Washington University School of Public Health and Health Services, April 2007. (Accessed July 26, 2007, at http://www.gwumc.edu/sphhs/about/rapidresponse/download/ RapidResponse_PDUFA.pdf.)
    • Wood S. Reauthorizing the Prescription Drug User Fee Act: how are PDUFA, the FDA budget, and drug safety related? Washington, DC: George Washington University School of Public Health and Health Services, April 2007. (Accessed July 26, 2007, at http://www.gwumc.edu/sphhs/about/rapidresponse/download/ RapidResponse_PDUFA.pdf.)
  • 3
    • 85030506151 scopus 로고    scopus 로고
    • FDA Arthritis Advisory Committee, Rockville, MD: Food and Drug Administration, April 12, 2007, Accessed July 26, 2007, at
    • FDA Arthritis Advisory Committee. Arcoxia (etoricoxib). Rockville, MD: Food and Drug Administration, April 12, 2007. (Accessed July 26, 2007, at http://www.fda.gov/ohrms/dockets/ac/07/transcripts/2007-4290t1-Part4.pdf.)
    • Arcoxia (etoricoxib)
  • 5
    • 85030517925 scopus 로고    scopus 로고
    • Center for Drug Evaluation and Research, Rockville, MD: Food and Drug Administration, June 13, 2007, Accessed July 26, 2007, at
    • Center for Drug Evaluation and Research. NDA 21-888, Zimulti (rimonabant). Rockville, MD: Food and Drug Administration, June 13, 2007. (Accessed July 26, 2007, at http://www.fda.gov/ohrms/dockets/ac/07/transcripts/ 2007-4306t1-Part1.pdf.)
    • NDA 21-888, Zimulti (rimonabant)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.