Sistema de Información Esencial en Terapéutica y Salud

@SIETES7

Última actualización: 21/11/2017
SIETES contiene 92130 citas

 
 
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3. Cita con resumen
Fralick M, Avorn J, Kesselheim AS. The price of crossing the border for medications. N Engl J Med 2017;377:311-3. [Ref.ID 101925]
4. Cita con resumen
Kesselheim AS, Donneyong M, Dal Pan GJ, Zhou EH, Avorn J, Schneeweiss S, Seeger JD. Changes in prescribing and healthcare resource utilization after FDA Drug Safety Communications involving zolpidem-containing medications. Pharmacoepidemiol Drug Saf 2017;26:712-21. [Ref.ID 101627]
5. Cita con resumen
Hwang TJ, Carpenter D, Lauffenburger JC, Wang B, Franklin JM, Kesselheim AS. Failure of investigational drugs in late-stage clinical development and publication of trial results. JAMA Intern Med 2016;176:1826-33. [Ref.ID 100788]
6. Cita con resumen
Kesselheim AS, Avorn J, Sarpatwari A. The high cost of prescription drugs in the United States: origins and prospects for reform. JAMA 2016;316:858-71. [Ref.ID 100589]
7. Cita con resumen
Kesselheim AS, Wang B, Franklin JM, Darrow JJ. Trends in utilization of FDA expedited drug development and approval programs, 1987-2014: cohort study. BMJ 2015;351:h4633. [Ref.ID 99588]
8. Cita con resumen
Kesselheim AS, Laggs LR, Sarpatwari A. Experience with the priority review voucher program for drug development. JAMA 2015;314:27 de octubre. [Ref.ID 99526]
9. Cita con resumen
Avorn J, Sarpatwari A, Kesselheim AS. Forbidden and permitted statements about medications - Loosening the rules. N Engl J Med 2015;373:967-73. [Ref.ID 99432]
10.Tiene citas relacionadas Cita con resumen
Sharfstein JM, Kesselheim AS. The safety of prescription drugs. JAMA 2015;314:233-4. [Ref.ID 99359]
11. Cita con resumen
Sarpatwari A, Avorn J, Kesselheim AS. Progress and hurdles for follow-on biologics. N Engl J Med 2015;372:2380-2. [Ref.ID 99297]
12. Cita con resumen
Kesselheim AS, Campbell EG, Schneeweiss S, Rausch P, Lappin BM, Zhou EH, Seeger JD, Brownstein JS, Woloshin S, Schwartz LM, Toomey T, Dal Pan GJ, Avorn J. Methodological approaches to evaluate the impact of FDA drug safety communications. Drug Saf 2015;38:565-75. [Ref.ID 99239]
13. Cita con resumen
Kesselheim AS, Bykov K, Avorn J, Tong A, Doherty M, Choudhry NK. Burden of changes in pill appearance for patients receiving generic cardiovascular medications after myocardial infarction: cohort and nested case - control studies. Ann Intern Med 2014;161:96-103. [Ref.ID 97814]
14. Cita con resumen
Ross JS, Kesselheim AS. Prescription-drug coupons - No such thing as a free lunch. N Engl J Med 2013;369:1188-9. [Ref.ID 96300]
15.Tiene citas relacionadas
Kesselheim AS. Drug company gifts to medical students: the hidden curriculum. BMJ 2013;346:8. [Ref.ID 94974]
16.Tiene citas relacionadas
Kesselheim AS, Misono AS, Shrank WH, Greene JA, Doherty M, Avorn J, Choudhry NK. Variations in pill appearance of antiepileptic drugs and the risk of nonadherence. JAMA Intern Med 2013;173:202-8. [Ref.ID 94940]
17. Cita con resumen
Kesselheim AS, Mello MM, Avorn J. FDA regulation of off-label drug promotion under attack. JAMA 2013;309:445-6. [Ref.ID 94907]
18. Cita con resumen
Kesselheim AS, Avorn J, Greene JA. Risk, responsibility, and generic drugs. N Engl J Med 2012;367:1679-81. [Ref.ID 93957]
19.Tiene citas relacionadas Cita con resumen
Kesselheim AS, Robertson CT, Myers JA, Rose SL, Gillet V, Ross KM, Glynn RJ, Joffe S, Avorn J. A randomized study of how physicians interpret research funding disclosures. N Engl J Med 2012;367:1119-27. [Ref.ID 93771]
20. Cita con resumen
Kesselheim AS, Myers JA, Avorn J. Characteristics risks of clinical trials to support approval of orphan vs nonorphan drugs for cancer. JAMA 2011;305:2320-6. [Ref.ID 91071]
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