O’Neill RT, Szarfman A. 2001. Some FDA perspectives on data mining for pediatric safety assessment. Current Therapeutic Research, Clinical and Experimental 62(9):650–663.


Rothman KJ, Lanes S, Sacks ST. 2004. The reporting odds ratio and its advantages over the proportional reporting ratio. Pharmacoepidemiology and Drug Safety 13:519–523.


Szarfman A, Machado SG, O’Neill RT. 2002. Use of screening algorithms and computer systems to efficiently signal higher-than-expected combinations of drugs and events in the US FDA’s spontaneous reports database. Drug Safety 25(6):381–392.


Truog RD. 1999. Commentary: Informed consent and research design in critical care medicine. Critical Care 3(3):R29–R33.


UK Collaborative ECMO Trial Group. 1996. UK collaborative randomised trial of neonatal extracorporeal membrane oxygenation. Lancet 348(9020):75–78.



The National Academies | 500 Fifth St. N.W. | Washington, D.C. 20001
Copyright © National Academy of Sciences. All rights reserved.
Terms of Use and Privacy Statement