Sistema de Información Esencial en Terapéutica y Salud

@SIETES7

Última actualización: 18/9/2019
SIETES contiene 92806 citas

 
 
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1. Cita con resumen
Wise J. Darzi calls for overhaul of safety incident reporting. BMJ 2016;352:i1434. [Ref.ID 100332]
2. Cita con resumen
Zorzela L, Golder S, Liu Y, Pilkington K, Hartling L, Joffe A, Loke Y, Vohra S. Quality of reporting in systematic reviews of adverse events: systematic review. BMJ 2014;348:f7668. [Ref.ID 97237]
3. Cita con resumen
Trenque T, Maura C, Herlem E, Vallet C, Sole E, Auriche P, Drame M. Reports of sexual disorders related to serotonin reuptake inhibitors in the French Pharmacovigilance Database: an example of underreporting. Drug Saf 2013;36:515-9. [Ref.ID 95771]
7. Cita con resumen
Pal SN, Duncombe C, Falzon D, Olsson S. WHO strategy for collecting safety data in public health programmes: complementing spontaneous reporting systems. Drug Saf 2013;36:75-81. [Ref.ID 94862]
8. Cita con resumen
Klopotowska JE, Wierenga PC, Smorenburg SM, Stuijt CCM, Arisz L, Kuks PFM, Dijkgraaf MGW, Lie-A-Huen L, de Rooij SE. Recognition of adverse drug events in older hospitalized medical patients. Eur J Clin Pharmacol 2013;69:75-85. [Ref.ID 94841]
9. Cita con resumen
Anónimo. Serotonergic medicines. Risk of reversible cerebral vasoconstriction syndrome (RCVS). New Zealand. WHO Pharmaceuticals Newsletter 2012;4:11-2. [Ref.ID 93679]
10. Cita con resumen
11. Cita con resumen
12.Tiene citas relacionadas Cita con resumen
Budnitz DS, Lovegrove MC, Shehab N. Emergency hospitalizations for adverse drug events. Author/editor response. N Engl J Med 2012;366:860. [Ref.ID 92476]
13.Tiene citas relacionadas Cita con resumen
Gnjidic D, Hilmer SN. Emergency hospitalizations for adverse drug events. N Engl J Med 2012;366:859. [Ref.ID 92475]
14.Tiene citas relacionadas Cita con resumen
Hohl CM, de Lemos J, Laban RBA. Emergency hospitalizations for adverse drug events. N Engl J Med 2012;366:858. [Ref.ID 92474]
15. Cita con resumen
Roehr B. US incident reporting systems do not capture most adverse events. BMJ 2012;344:6. [Ref.ID 92264]
16. Cita con resumen
Anónimo. Reacciones adversas a medicamentos registradas en el Conjunto Mínimo Básico de Datos (CMBD). Boletín de Farmacovigilancia de la Región de Murcia 2011;23:1-2. [Ref.ID 92092]
17.Tiene citas relacionadas Cita con resumen
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]
18.Tiene citas relacionadas Cita con resumen
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]
19.Tiene citas relacionadas Cita con resumen
Carvajal A, García-Ortega P, Sáinz M, Velasco V, Salado I, Martín Arias LH, Eiros JM, Pérez Rubio A, Castrodeza J. Adverse events associated with pandemic influenza vaccines: Comparison of the results of a follow-up study with those coming from spontaneous reporting. Vaccine 2011;29:519-22. [Ref.ID 89853]
20.Enlace a cita original
Cox AR, Anton C, McDowell SE, Marriott JF, Ferner RE. Correlates of spontaneous reporting of adverse drug reactions within primary care: the paradox of low prescribers who are high reporters. Br J Clin Pharmacol 2010;69:529-34. [Ref.ID 88443]
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