ReviewDrug safety2026
Analytic Misjudgment of Drug Safety Evidence and Causality: From the Prosecutor's Fallacy and Simpson's Paradox to Artificial Intelligence.
Review in Drug safety, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Drug safety assessment, particularly in the post-marketing setting, is especially vulnerable to analytic misjudgment because it relies on heterogeneous evidence streams, incomplete data, infrequent events, and decisions made under substantial uncertainty. Recurring sources of error include misinterpretation of conditional probabilities, conflation of association with causation, inappropriate denominator and comparator selection, inadequate consideration of background incidence and confounding, aggregation artifacts such as Simpson's paradox, and overinterpretation of exploratory findings arising from multiplicity or repeated testing. Misjudgment may be further amplified by spontaneous reporting data that lack explicit exposure denominators and are susceptible to reporting bias, by fragile or incomplete meta-analyses, and by premature regulatory or public responses to weak or incompletely contextualized signals. Using selected real-world case studies and conceptual examples, this narrative review illustrates how such errors arise and propagate across clinical, regulatory, and public domains, and how they can materially influence causality assessment and decision making. The paper also discusses how artificial intelligence (AI), if implemented without transparency, bias assessment, and clinical oversight, may amplify rather than reduce these vulnerabilities. Greater analytic discipline, clearer communication of uncertainty, triangulation across evidence streams, and careful governance of emerging AI-enabled tools are needed to support more reliable drug safety evaluation.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.