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Journal Abstract Search

479 related items for PubMed ID: 18046024

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  • 23. The FDA and drug safety: a proposal for sweeping changes.
    Furberg CD, Levin AA, Gross PA, Shapiro RS, Strom BL.
    Arch Intern Med; 2006 Oct 09; 166(18):1938-42. PubMed ID: 17030825
    [Abstract] [Full Text] [Related]

  • 24. Vioxx's history and the need for better procedures and better testing.
    Gilhooley M.
    Seton Hall Law Rev; 2007 Oct 09; 37(4):941-68. PubMed ID: 18363218
    [No Abstract] [Full Text] [Related]

  • 25. FDA attempting to overcome major roadblocks in monitoring drug safety.
    Zielinski SL.
    J Natl Cancer Inst; 2005 Jun 15; 97(12):872-3. PubMed ID: 15956645
    [No Abstract] [Full Text] [Related]

  • 26. The Supreme Court, preemption, and malpractice liability.
    Kesselheim AS, Studdert DM.
    N Engl J Med; 2009 Feb 05; 360(6):559-61. PubMed ID: 19196672
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  • 27. Drug-review deadlines and safety problems.
    Nardinelli C, Lanthier M, Temple R.
    N Engl J Med; 2008 Jul 03; 359(1):95-6; author reply 96-8. PubMed ID: 18596282
    [No Abstract] [Full Text] [Related]

  • 28. The marketplace can't give us the drug safety data we need.
    Avorn J.
    MedGenMed; 2007 Feb 09; 9(1):29. PubMed ID: 17435636
    [No Abstract] [Full Text] [Related]

  • 29. Ensuring the safety of genotech drugs through implied warranty theory.
    Serra WM.
    Am J Law Med; 1997 Feb 09; 23(2-3):363-81. PubMed ID: 9262761
    [No Abstract] [Full Text] [Related]

  • 30. Deterring inefficient pharmaceutical litigation: an economic rationale for the FDA regulatory compliance defense.
    Viscusi WK, Rowland SR, Dorfman HL, Walsh CJ.
    Spec Law Dig Health Care Law; 1996 Mar 09; (205):9-52. PubMed ID: 10156421
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  • 31. The unfinished business of U.S. drug safety regulation.
    Evans BJ, Flockhart DA.
    Food Drug Law J; 2006 Mar 09; 61(1):45-63. PubMed ID: 16838457
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  • 35. FDA's regulation of prescription drug labeling: a role for implied preemption.
    Kendrick LC.
    Food Drug Law J; 2007 Mar 09; 62(1):227-47. PubMed ID: 17444031
    [No Abstract] [Full Text] [Related]

  • 36. Pharmaceuticals and medical devices: FDA oversight. Issue brief.
    Thomson Reuters/West.
    Issue Brief Health Policy Track Serv; 2011 Jan 03; ():1-39. PubMed ID: 21374841
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  • 37. Impossible? Outlawing state safety laws for generic drugs.
    Glantz LH, Annas GJ.
    N Engl J Med; 2011 Aug 25; 365(8):681-3. PubMed ID: 21830958
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  • 38. Statistical, epidemiological, and risk-assessment approaches to evaluating safety of vaccines throughout the life cycle at the Food and Drug Administration.
    Ball R, Horne D, Izurieta H, Sutherland A, Walderhaug M, Hsu H.
    Pediatrics; 2011 May 25; 127 Suppl 1():S31-8. PubMed ID: 21502249
    [Abstract] [Full Text] [Related]

  • 39. Drug safety and drug efficacy: two sides of the same coin.
    Young RC, Friedman MA, Schilsky RL, Sigal EV.
    Clin Cancer Res; 2007 May 01; 13(9):2533-4. PubMed ID: 17473179
    [No Abstract] [Full Text] [Related]

  • 40. How the FDA manages drug safety with black box warnings, use restrictions, and drug removal, with attention to gastrointestinal medications.
    Ehrenpreis ED, Ciociola AA, Kulkarni PM, FDA-Related Matters Committee of the American College of Gastroenterology.
    Am J Gastroenterol; 2012 Apr 01; 107(4):501-4. PubMed ID: 22475958
    [No Abstract] [Full Text] [Related]

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