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PUBMED FOR HANDHELDS

Journal Abstract Search


863 related items for PubMed ID: 11802586

  • 21. Decision support methods for the detection of adverse events in post-marketing data.
    Hauben M, Bate A.
    Drug Discov Today; 2009 Apr; 14(7-8):343-57. PubMed ID: 19187799
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  • 23. 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
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  • 27. 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
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  • 32. FDA guidance document on monitoring delayed adverse events a good first start.
    Williams DA.
    Mol Ther; 2005 Dec 09; 12(6):991-2. PubMed ID: 16271514
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  • 34. Postmarketing surveillance of potentially fatal reactions to oncology drugs: potential utility of two signal-detection algorithms.
    Hauben M, Reich L, Chung S.
    Eur J Clin Pharmacol; 2004 Dec 09; 60(10):747-50. PubMed ID: 15619136
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  • 35. Finding, evaluating, and managing drug-related risks: approaches taken by the US Food and Drug Administration (FDA).
    Weaver J, Grenade LL, Kwon H, Avigan M.
    Dermatol Ther; 2009 Dec 09; 22(3):204-15. PubMed ID: 19453344
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  • 37. MedWatch: the FDA medical products reporting program.
    Rheinstein PH.
    Am Fam Physician; 1993 Sep 15; 48(4):636-8. PubMed ID: 8379493
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  • 38. The Vaccine Safety Datalink project.
    DeStefano F, Vaccine Safety Datalink Research Group.
    Pharmacoepidemiol Drug Saf; 2001 Sep 15; 10(5):403-6. PubMed ID: 11802585
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  • 39. Postmarketing surveillance.
    Oleen MA.
    Can J Hosp Pharm; 1987 Oct 15; 40(5):171-2, 179-80. PubMed ID: 10284449
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  • 40. Safety in numbers--monitoring risk in approved drugs.
    Okie S.
    N Engl J Med; 2005 Mar 24; 352(12):1173-6. PubMed ID: 15788493
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