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Pubmed for Handhelds
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]