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False Discovery Rate Estimation for Frequentist Pharmacovigilance Signal Detection Methods
Authors:I Ahmed  C Dalmasso  F Haramburu  F Thiessard  P Broët  P Tubert-Bitter
Institution:Inserm U780, Villejuif, F-94807, France;Univ Paris-Sud, IFR69, Villejuif, F-94807, France;JE2492, Faculty of Medicine Paris-Sud, Univ Paris-Sud, Villejuif, F-94807, France;Inserm U657, Bordeaux, F-33076, France;Pellegrin Hospital, Bordeaux, F-33076, France;LESIM, Univ Victor Segalen Bordeaux 2, Bordeaux, F-33076, France;Inserm U897, Bordeaux, F-33076, France
Abstract:Summary .  Pharmacovigilance systems aim at early detection of adverse effects of marketed drugs. They maintain large spontaneous reporting databases for which several automatic signaling methods have been developed. One limit of those methods is that the decision rules for the signal generation are based on arbitrary thresholds. In this article, we propose a new signal-generation procedure. The decision criterion is formulated in terms of a critical region for the P-values resulting from the reporting odds ratio method as well as from the Fisher's exact test. For the latter, we also study the use of mid-P-values. The critical region is defined by the false discovery rate, which can be estimated by adapting the P-values mixture model based procedures to one-sided tests. The methodology is mainly illustrated with the location-based estimator procedure. It is studied through a large simulation study and applied to the French pharmacovigilance database.
Keywords:False discovery rate  Fisher's exact test  Location-based estimator  Mid-P-values  Mixture model  Multiple comparisons  One-sided P-values  Pharmacovigilance  Reporting odds ratio
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