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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 [Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]