Hepatitis B vaccine and first episodes of central nervous system demyelinating disorders: a comparison between reported and expected number of cases, British Journal of Clinical Pharmacology, vol.36, issue.5, pp.51489-490, 2001. ,
DOI : 10.1046/j.1365-2125.2001.01364.x
Spontaneous reporting: how many cases are required to trigger a warning? [see comments], British Journal of Clinical Pharmacology, vol.32, issue.4, pp.407-408, 1991. ,
DOI : 10.1111/j.1365-2125.1991.tb03922.x
Reports of hypoglycaemia associated with the use of ACE inhibitors and other drugs: a case/non-case study in the French pharmacovigilance system database, British Journal of Clinical Pharmacology, vol.44, issue.5, pp.44513-518, 1997. ,
DOI : 10.1046/j.1365-2125.1997.00615.x
Comparing the toxicity of two drugs in the framework of spontaneous reporting: A confidence interval approach, Journal of Clinical Epidemiology, vol.49, issue.1 ,
DOI : 10.1016/0895-4356(95)00537-4
On the assessment of adverse drug reactions from spontaneous reporting systems: the influence of under-reporting on odds ratios, Statistics in Medicine, vol.126, issue.14, pp.2027-2044, 2002. ,
DOI : 10.1002/sim.1157
A Bayesian neural network method for adverse drug reaction signal generation, European Journal of Clinical Pharmacology, vol.54, issue.4, pp.315-321, 1998. ,
DOI : 10.1007/s002280050466
Bayesian Data Mining in Large Frequency Tables, with an Application to the FDA Spontaneous Reporting System, The American Statistician, vol.13, issue.3 ,
DOI : 10.2307/1164724
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 Saf, issue.6, pp.25381-392, 2002. ,
Use of proportional reporting ratios (PRRs) for signal generation from spontaneous adverse drug reaction reports, Pharmacoepidemiology and Drug Safety, vol.8, issue.6, pp.483-486, 2001. ,
DOI : 10.1002/pds.677
Bayesian pharmacovigilance signal detection methods revisited in a multiple comparison setting, Statistics in Medicine, vol.23, issue.6, pp.281774-1792, 2009. ,
DOI : 10.1002/pds.771
False Discovery Rate Estimation for Frequentist Pharmacovigilance Signal Detection Methods, Biometrics, vol.13, issue.1, pp.301-309, 2010. ,
DOI : 10.1111/j.1541-0420.2009.01262.x
Evaluation of statistical association measures for the automatic signal generation in pharmacovigilance, IEEE Transactions on Information Technology in Biomedicine, vol.9, issue.4, pp.518-527, 2005. ,
DOI : 10.1109/TITB.2005.855566A
URL : https://hal.archives-ouvertes.fr/hal-00396036
Pharmacovigilance Data Mining With Methods Based on False Discovery Rates: A Comparative Simulation Study, Clinical Pharmacology & Therapeutics, vol.57, issue.4, pp.492-498, 2010. ,
DOI : 10.1016/0895-4356(92)90088-5
Quantitative signal detection using spontaneous ADR reporting, Pharmacoepidemiology and Drug Safety, vol.12, issue.6, pp.427-436, 2009. ,
DOI : 10.1002/pds.1742
Validation of Statistical Signal Detection Procedures in EudraVigilance Post-Authorization Data, Drug Safety, vol.28, issue.11, pp.475-487, 2010. ,
DOI : 10.2165/11534410-000000000-00000
Time-to-Signal Comparison for Drug Safety Data-Mining Algorithms vs. Traditional Signaling Criteria, Clinical Pharmacology & Therapeutics, vol.41, issue.6, pp.600-606, 2009. ,
DOI : 10.1111/j.1365-2125.2004.02203.x
Tubert-Bitter P: Early detection of pharmacovigilance signals with automated methods based on false discovery rates: a comparative study, Drug Saf, vol.2012, issue.6, pp.35495-506 ,
Modelling the Time to Onset of Adverse Reactions with Parametric Survival Distributions, Drug Safety, vol.28, issue.11, pp.417-434, 2010. ,
DOI : 10.2165/11532850-000000000-00000
Using time-to-onset for detecting safety signals in spontaneous reports of adverse events following immunization: a proof of concept study, Pharmacoepidemiology and Drug Safety, vol.25, issue.6, pp.603-610 ,
DOI : 10.1002/pds.3226
A Signal Detection Method to Detect Adverse Drug Reactions Using a Parametric Time-to-Event Model in Simulated Cohort Data, Drug Safety, vol.16, issue.4, pp.599-610 ,
DOI : 10.2165/11599740-000000000-00000
Nonparametric analysis of truncated survival data, with application to AIDS, Biometrika, vol.75, issue.3, pp.515-523, 1988. ,
DOI : 10.1093/biomet/75.3.515
Regression models for right truncated data with applications to AIDS incubation times and reporting lags, Stat Sin, vol.1, pp.19-32, 1991. ,
Estimation of the denominator in spontaneous reporting, Methodological Approaches in Pharmacoepidemiology: Application to Spontaneous Reporting, pp.51-70, 1993. ,
A Language and Environment for Statistical Computing. R Foundation for Statistical Computing ,
Sources of Information on Lymphoma Associated with Anti-Tumour Necrosis Factor Agents, Drug Safety, vol.72, issue.6, pp.34577-585, 2011. ,
DOI : 10.2165/11590200-000000000-00000
An Introduction to the Bootstrap, 1993. ,
DOI : 10.1007/978-1-4899-4541-9
Bootstrap methods for truncated and censored data, Stat Sin, vol.6, pp.509-530, 1996. ,
Mathematical models in adverse drug reaction assessment In Iatrogenic Diseases, 1986. ,
Spontaneous reporting of adverse drug reactions: who reports and what?, Pharmacoepidemiology and Drug Safety, vol.7, issue.5, pp.323-329, 1998. ,
DOI : 10.1002/(SICI)1099-1557(199809/10)7:5<323::AID-PDS374>3.0.CO;2-8
Temporal trends in spontaneous reporting of unlabelled adverse drug reactions, British Journal of Clinical Pharmacology, vol.44, issue.3, pp.299-301, 1997. ,
DOI : 10.1046/j.1365-2125.1997.t01-1-00573.x
Under-reporting of adverse drug reactions in general practice, British Journal of Clinical Pharmacology, vol.43, issue.2, pp.177-181, 1997. ,
DOI : 10.1046/j.1365-2125.1997.05417.x
Rates of Spontaneous Reporting of Adverse Drug Reactions in France, JAMA: The Journal of the American Medical Association, vol.288, issue.13, pp.1588-1588, 2002. ,
DOI : 10.1001/jama.288.13.1588
Power and weakness of spontaneous reporting: A probabilistic approach, Journal of Clinical Epidemiology, vol.45, issue.3 ,
DOI : 10.1016/0895-4356(92)90088-5
Inference Based on Retrospective Ascertainment: An Analysis of the Data on Transfusion-Related AIDS, Journal of the American Statistical Association, vol.7, issue.406, pp.360-372, 1989. ,
DOI : 10.1046/j.1537-2995.1987.27587320525.x
Biased Sampling of Cohorts in Epidemiology, In Encyclopedia of Biostatistics, vol.1, pp.338-350, 1998. ,
Statistical Models and Methods for Lifetime Data New Jersey: Wiley; 2003. 37. Keiding N: Nonparametric estimation under truncation, In Encyclopedia of Statistical Sciences, vol.14, pp.8775-8777, 2006. ,
Bivariate estimation with right-truncated data, JAmStat Assoc, issue.435, pp.911152-1165, 1996. ,
Regression models for truncated survival data, Scandinavian J Stat, pp.193-213, 1992. ,
Estimating time-to-onset of adverse drug reactions from spontaneous reporting databases, BMC Medical Research Methodology, vol.91, issue.435, p.17, 2014. ,
DOI : 10.1080/01621459.1989.10478780
URL : https://hal.archives-ouvertes.fr/inserm-00946044