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Pubmed for Handhelds

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Journal Abstract Search

179 related items for PubMed ID: 23920875

  • 1. Standardizing drug adverse event reporting data.
    Wang L, Jiang G, Li D, Liu H.
    Stud Health Technol Inform; 2013; 192():1101. PubMed ID: 23920875
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  • 6. Thrombotic events associated with C1 esterase inhibitor products in patients with hereditary angioedema: investigation from the United States Food and Drug Administration adverse event reporting system database.
    Gandhi PK, Gentry WM, Bottorff MB.
    Pharmacotherapy; 2012 Oct; 32(10):902-9. PubMed ID: 23033229
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  • 15. An experimental investigation of masking in the US FDA adverse event reporting system database.
    Wang HW, Hochberg AM, Pearson RK, Hauben M.
    Drug Saf; 2010 Dec 01; 33(12):1117-33. PubMed ID: 21077702
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  • 16. Hypersensitivity reactions to anticancer agents: data mining of the public version of the FDA adverse event reporting system, AERS.
    Kadoyama K, Kuwahara A, Yamamori M, Brown JB, Sakaeda T, Okuno Y.
    J Exp Clin Cancer Res; 2011 Oct 05; 30(1):93. PubMed ID: 21970649
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  • 19. Quality assessment of spontaneous triggered adverse event reports received by the Food and Drug Administration.
    Brajovic S, Piazza-Hepp T, Swartz L, Dal Pan G.
    Pharmacoepidemiol Drug Saf; 2012 Jun 05; 21(6):565-70; discussion 571-2. PubMed ID: 22359404
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