Sistema de Información Esencial en Terapéutica y Salud


Última actualización: 25/2/2021
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Mehra MR, Desai SS, Ruschitzka F, Patel AN. Hydroxychloroquine or chloroquine with or without a macrolide for treatment of COVID-19: a multinational registry analysis. Lancet 2020:22 de mayo. [Ref.ID 103632]
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Anónimo. FDA to evaluate increased risk of heart -related death and death from all causes with the gout medicine febuxostat (Uloric). U.S. Food and Drug Administration 2017:15 de noviembre. [Ref.ID 102144]
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Psaty BM, Goodman SN, Breckenridge A. Advances in regulatory science at the Food and Drug Administration. JAMA 2013;309:2103-4. [Ref.ID 95457]
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Jha AK, Classen DC. Getting moving on patient safety - Harnessing electronic data for safer care. N Engl J Med 2011;365:1756-8. [Ref.ID 91643]
Qato DM, Alexander GC. Improving the Food and Drug Administration's mandate to ensure postmarketing drug safety. JAMA 2011;306:1595-6. [Ref.ID 91546]
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Classen DC, Resar R, Griffin F, Federico F, Frankel T, Kimmel N, Whittington JC, Frankel A, Seger A, James BC. 'Global trigger tool' shows that adverse events in hospitals may be ten times greater than previously measured. Health Affairs 2011;30:581-9. [Ref.ID 90387]
Arana A, Allen S, Burkowitz J, Fantoni V, Ghatnekar O, Rico MT, Vanhaverbeke N, Wentworth CE, Brosa M, Arellano FM. Infliximab paediatric Crohn's disease educational plan: a European, cross-sectional, multicentre evaluation. Drug Saf 2010;33:489-501. [Ref.ID 88648]
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