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| Φαρμακοεπαγρύπνηση PRR/ROR× | Πληθυσμιακή Φαρμακοδυναμική Μοντελοποίηση× | |
|---|---|---|
| Πεδίο | Φαρμακολογία | Φαρμακολογία |
| Οικογένεια | Process / pipeline | Process / pipeline |
| Έτος προέλευσης≠ | 2002 | 1992 |
| Δημιουργός≠ | Arne Melander and colleagues | Lewis Sheiner and Stephen Roush |
| Τύπος≠ | safety signal detection | dose-response modeling |
| Θεμελιώδης πηγή≠ | 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 ↗ | Dahlström, B., & Nyberg, L. (1993). Population pharmacokinetics and pharmacodynamics. Clinical Pharmacokinetics, 24(1), 45-57. link ↗ |
| Εναλλακτικές ονομασίες≠ | PRR, ROR, signal detection, adverse event monitoring | PopPD, population PD, hierarchical PD modeling |
| Συναφείς | 3 | 3 |
| Σύνοψη≠ | 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. | Population pharmacodynamic (PopPD) modeling integrates pharmacokinetics with individual dose-response relationships across patient populations to characterize drug efficacy and tolerability. Pioneered by Lewis Sheiner and colleagues, PopPD accounts for inter-individual variability in drug effects and enables rational dose optimization and response prediction. |
| ScholarGateΣύνολο δεδομένων ↗ |
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