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The REporting of A Disproportionality Analysis for DrUg Safety Signal Detection Using Individual Case Safety Reports in PharmacoVigilance (READUS-PV): Explanation and Elaboration

Abstract

In pharmacovigilance, disproportionality analyses based on individual case safety reports are widely used to detect safety signals. Unfortunately, publishing disproportionality analyses lacks specific guidelines, often leading to incomplete and ambiguous reporting, and carries the risk of incorrect conclusions when data are not placed in the correct context. The REporting of A Disproportionality analysis for drUg Safety signal detection using individual case safety reports in PharmacoVigilance (READUS-PV) statement was developed to address this issue by promoting transparent and comprehensive reporting of disproportionality studies. While the statement paper explains in greater detail the procedure followed to develop these guidelines, with this explanation paper we present the 14 items retained for READUS-PV guidelines, together with an in-depth explanation of their rationale and bullet points to illustrate their practical implementation. Our primary objective is to foster the adoption of the READUS-PV guidelines among authors, editors, peer reviewers, and readers of disproportionality analyses. Enhancing transparency, completeness, and accuracy of reporting, as well as proper interpretation of their results, READUS-PV guidelines will ultimately facilitate evidence-based decision making in pharmacovigilance.

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References
1.
Gauffin O, Brand J, Vidlin S, Sartori D, Asikainen S, Catala M . Supporting Pharmacovigilance Signal Validation and Prioritization with Analyses of Routinely Collected Health Data: Lessons Learned from an EHDEN Network Study. Drug Saf. 2023; 46(12):1335-1352. PMC: 10684396. DOI: 10.1007/s40264-023-01353-w. View

2.
Bailey C, Peddie D, Wickham M, Badke K, Small S, Doyle-Waters M . Adverse drug event reporting systems: a systematic review. Br J Clin Pharmacol. 2016; 82(1):17-29. PMC: 4917803. DOI: 10.1111/bcp.12944. View

3.
Evans S, Waller P, Davis S . Use of proportional reporting ratios (PRRs) for signal generation from spontaneous adverse drug reaction reports. Pharmacoepidemiol Drug Saf. 2002; 10(6):483-6. DOI: 10.1002/pds.677. View

4.
Reich C, Ryan P, Schuemie M . Alternative outcome definitions and their effect on the performance of methods for observational outcome studies. Drug Saf. 2013; 36 Suppl 1:S181-93. DOI: 10.1007/s40264-013-0111-1. View

5.
Moola S, Munn Z, Sears K, Sfetcu R, Currie M, Lisy K . Conducting systematic reviews of association (etiology): The Joanna Briggs Institute's approach. Int J Evid Based Healthc. 2015; 13(3):163-9. DOI: 10.1097/XEB.0000000000000064. View