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Home›Pharmacology›Pharmacovigilance PRR/ROR
Process / pipelinePharmacoepidemiology

Pharmacovigilance PRR/ROR

Proportional Reporting Ratio and Reporting Odds Ratio for Pharmacovigilance · Also known as: PRR, ROR, signal detection, adverse event monitoring

Proportional Reporting Ratio (PRR) and Reporting Odds Ratio (ROR) are statistical methods for detecting safety signals in spontaneous adverse event reporting databases. Developed and formalized by researchers in the early 2000s, these measures identify drug-adverse event associations that warrant further investigation.

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Pharmacovigilance PRR/ROR
Caco-2 PermeabilityPopulation Pharmacodynam…Arrhenius Stability

When to use it

Use PRR and ROR for disproportionality analysis of spontaneous adverse event reporting databases (e.g., FDA FAERS, EudraVigilance) when screening for drug-adverse event signals — particularly in post-marketing pharmacovigilance where randomized trial data are unavailable or insufficient for rare events.

Strengths & limitations

Strengths
  • Signal detection at scale: screens millions of reports across thousands of drug-event pairs rapidly
  • Established regulatory acceptance: PRR and ROR are standard methods used by EMA, FDA, and WHO-Uppsala
  • No comparator drug needed for ROR: odds ratio formulation is symmetric and easy to interpret
  • Early warning system: can detect novel safety signals before formal epidemiological studies are feasible
  • Publicly available databases: FAERS and EudraVigilance provide large, continuously updated data sources
Limitations
  • Confounding by indication: drugs prescribed for specific diseases may show spurious associations with disease-related events
  • Notoriety bias: media attention increases reporting of a specific drug-event pair, inflating signals
  • Under-reporting: spontaneous reporting captures only an estimated 1–10% of actual adverse events
  • No denominator: cannot calculate incidence rates; only relative reporting frequencies are available
  • Masking: a dominant drug-event pair can suppress signals for co-reported drugs (pooled background effect)

Sources

  1. Szarfman, A., Tonning, J. M., Doraiswamy, P. M., & Osgood, D. J. (2002). Pharmacovigilance in the post-marketing setting: establishing causal links between drugs and adverse events. Drug Safety, 25(9), 619-631. link ↗
  2. van Puijenbroek, E. P., Bate, A., Leufkens, H. G., Lindquist, M., Orre, R., & Egberts, A. C. (2002). A comparison of measures of disproportionality for signal detection in spontaneous adverse drug reaction reporting. Pharmacoepidemiology and Drug Safety, 11(1), 3-10. DOI: 10.1002/pds.668 ↗

How to cite this page

ScholarGate. (2026, June 3). Proportional Reporting Ratio and Reporting Odds Ratio for Pharmacovigilance. ScholarGate. https://scholargate.app/en/pharmacology/pharmacovigilance-prr-ror

Related methods

Caco-2 PermeabilityPopulation Pharmacodynamics

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Referenced by

Arrhenius Stability

Similar methods

Meta-analytic Phase IV StudyBayesian Case SeriesBayesian Phase IV studyMatched Phase IV StudyRisk-adjusted Phase IV studyProspective Phase IV StudySelf-Controlled Case SeriesPragmatic phase IV study

Related reference concepts

Signal Detection and Statistical AssessmentRisk Identification and CharacterizationPharmacovigilance, Adverse Event Reporting, and Post-Market SurveillancePharmacovigilance Systems and ReportingSpontaneous (Passive) Adverse Event ReportingAdverse Event Reporting and Pharmacovigilance

Spotted an issue on this page? Report or suggest a fix →

ScholarGate — Pharmacovigilance PRR/ROR (Proportional Reporting Ratio and Reporting Odds Ratio for Pharmacovigilance). Retrieved 2026-07-21 from https://scholargate.app/en/pharmacology/pharmacovigilance-prr-ror · Dataset: https://doi.org/10.5281/zenodo.20539026
Quick facts
Originator
Arne Melander and colleagues
Subfamily
Pharmacoepidemiology
Year
2002
Type
safety signal detection
Related methods
Caco-2 PermeabilityPopulation Pharmacodynamics
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