Several authors (JB, RD, SA, MR, LH, DR, DB, DS, JG, MG, RP) received partial funding from Pfizer Inc, two authors (KP, RR) are employees of Pfizer Inc and hold stock in the company, one author has been paid as a general consultant on drug safety issues by several pharmaceutical firms (RD), and one author (AC) is a part-time employee of a contract research organization that receives funding from pharmaceutical companies and the FDA. The study sponsors had no input into the collection of data, interpretation or results, or the decision to publish the findings.
Early adverse drug event signal detection within population-based health networks using sequential methods: key methodologic considerations†
Article first published online: 15 JAN 2009
Copyright © 2009 John Wiley & Sons, Ltd.
Pharmacoepidemiology and Drug Safety
Volume 18, Issue 3, pages 226–234, March 2009
How to Cite
Brown, J. S., Kulldorff, M., Petronis, K. R., Reynolds, R., Chan, K. A., Davis, R. L., Graham, D., Andrade, S. E., Raebel, M. A., Herrinton, L., Roblin, D., Boudreau, D., Smith, D., Gurwitz, J. H., Gunter, M. J. and Platt, R. (2009), Early adverse drug event signal detection within population-based health networks using sequential methods: key methodologic considerations. Pharmacoepidem. Drug Safe., 18: 226–234. doi: 10.1002/pds.1706
- Issue published online: 20 FEB 2009
- Article first published online: 15 JAN 2009
- Manuscript Accepted: 4 DEC 2008
- Manuscript Revised: 29 NOV 2008
- Manuscript Received: 23 SEP 2008
- AHRQ. Grant Number: 2U18HS010391
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