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PUBMED FOR HANDHELDS

Journal Abstract Search


183 related items for PubMed ID: 19236120

  • 1. Drug-versus-drug adverse event rate comparisons: a pilot study based on data from the US FDA Adverse Event Reporting System.
    Hochberg AM, Pearson RK, O'Hara DJ, Reisinger SJ.
    Drug Saf; 2009; 32(2):137-46. PubMed ID: 19236120
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  • 2. 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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  • 4. AERS spider: an online interactive tool to mine statistical associations in Adverse Event Reporting System.
    Grigoriev I, zu Castell W, Tsvetkov P, Antonov AV.
    Pharmacoepidemiol Drug Saf; 2014 Aug 01; 23(8):795-801. PubMed ID: 24677538
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  • 9. How safe are recently FDA-approved antimicrobials? A review of the FDA adverse event reporting system database.
    Khadem TM, van Manen RP, Brown J.
    Pharmacotherapy; 2014 Dec 01; 34(12):1324-9. PubMed ID: 25421400
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  • 11. 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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  • 14. Platinum agent-induced hypersensitivity reactions: data mining of the public version of the FDA adverse event reporting system, AERS.
    Sakaeda T, Kadoyama K, Yabuuchi H, Niijima S, Seki K, Shiraishi Y, Okuno Y.
    Int J Med Sci; 2011 Oct 05; 8(4):332-8. PubMed ID: 21611115
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  • 15. Safety of lovastatin/extended release niacin compared with lovastatin alone, atorvastatin alone, pravastatin alone, and simvastatin alone (from the United States Food and Drug Administration adverse event reporting system).
    Alsheikh-Ali AA, Karas RH.
    Am J Cardiol; 2007 Feb 01; 99(3):379-81. PubMed ID: 17261402
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  • 16. Standardizing drug adverse event reporting data.
    Wang L, Jiang G, Li D, Liu H.
    Stud Health Technol Inform; 2013 Feb 01; 192():1101. PubMed ID: 23920875
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  • 17. Antimicrobials and the risk of torsades de pointes: the contribution from data mining of the US FDA Adverse Event Reporting System.
    Poluzzi E, Raschi E, Motola D, Moretti U, De Ponti F.
    Drug Saf; 2010 Apr 01; 33(4):303-14. PubMed ID: 20297862
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