Evidence map›Paper›PMID 41726499›Full record

ArticleAMIA ... Annual Symposium proceedings. AMIA Symposium2024

Revisiting Disproportionality: Prescription-Adjusted and TF-IDF-Inspired Metrics for Post-Market ADR Detection.

Ijay Kaz-Onyeakazi, Heejun Kim

Abstract read
In one paragraph

Article in AMIA ... Annual Symposium proceedings. AMIA Symposium, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Ijay Kaz-OnyeakaziUniversity of North Texas, Denton, Texas, United States.
Heejun KimUniversity of North Texas, Denton, Texas, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adverse drug reaction (ADR) detection in post-market surveillance is limited by underreporting and the absence of drug utilization data. This study proposes three signal detection metrics-including a TF-IDF-inspired method (EF-IDF) and two prescription-adjusted measures-to improve pharmacovigilance, using ADHD medications and the FDA Adverse Event Reporting System (FAERS) as a case study. We standardized drug and ADR entities, integrated prescription data from Bloomberg Intelligence, and evaluated performance across 12 ingredients using precision-at-10%. EF-IDF achieved the highest mean precision (0.56), significantly outperforming traditional PRR and prescription-adjusted metrics. Correlation analysis showed that prescription volume negatively influenced all metrics, particularly EF-IDF, underscoring the role of contextual factors in ADR detection. Despite limitations in temporal granularity and the lack of prescription data specific to ADHD use, this work demonstrates the value of bias-aware, data-integrated methods for signal detection. Future directions include temporal modeling and more targeted identification of ADHD-related prescriptions using public data.

Indexed as

Adverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse ReactionsPharmacovigilanceProduct Surveillance, PostmarketingAttention Deficit Disorder with HyperactivityHumansUnited StatesUnited States Food and Drug Administration

Identifiers

PMID41726499
PMCPMC12919448

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.