This is the program for the 2010 Joint Statistical Meetings in Vancouver, British Columbia.

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Keyword Search Criteria: Adverse Event returned 8 record(s)
Sunday, 08/01/2010
Sequential Analytic Methods for Prospective Drug Safety Surveillance
Lingling Li, Harvard Medical School/Harvard Pilgrim Health Care Institute
4:30 PM

Assessing the Causal Effect of Treatment Dosages in the Presence of Self-Selection
Xin Gao, University of Michigan; Michael R. Elliott, University of Michigan
5:05 PM

Monday, 08/02/2010
An Individual-Patient Meta-Analytic Mixed Model with Repeated Measures and Time-Dependent Covariates: An Application to Adverse Event Data
Sofia Paul, Novartis Pharmaceuticals Corporation; Stephanie Ann Kovalchik, University of California, Los Angeles; Jing Hu, Novartis Pharmaceuticals Corporation; Glen Laird, Novartis Pharmaceuticals Corporation
2:20 PM

Tuesday, 08/03/2010
Identifying Temporal Pattern of Adverse Events in Drug-Eluting Stents Studies
Aijun Song, Boston Scientific Corporation; Huyuan Yang, Boston Scientific Corporation; Hsini Terry Liao, Boston Scientific Corporation; Jeff Hersh, Boston Scientific Corporation
9:55 AM

Meta-Analysis for Rare Adverse Event Data from Clinical Trials
Brenda Crowe, Eli Lilly and Company
10:35 AM

Wednesday, 08/04/2010
The Reliability of Signal Analysis in the Adverse Events Setting of Priorities
Qian Graves, FDA/CFSAN; Peng T. Liu, FDA; Stuart Chirtel, FDA/CFSAN; Curtis Barton, FDA/CFSAN; Debra Street, FDA/CFSAN
9:20 AM

Sparse Data in Meta-Analysis: Parametric and Semiparametric Models and Parameterization Issues
Arpita Chatterjee, Northern Illinois University; Sanjib Basu, Northern Illinois University
11:15 AM

Thursday, 08/05/2010
Bayesian Hierarchical Models for Detecting Safety Signals in Clinical Trials
Haijun Ma, Amgen Inc.; Amy Xia, Amgen Inc.; Bradley P. Carlin, University of Minnesota
10:35 AM




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