Evidence map›Paper›PMID 40736603›Full record

ReviewInternational journal of clinical pharmacy2025

Artificial intelligence in pharmacovigilance: a narrative review and practical experience with an expert-defined Bayesian network tool.

Rogério Caixinha Algarvio, Jaime Conceição, Pedro Pereira Rodrigues, Inês Ribeiro, Renato Ferreira-da-Silva

Abstract readReview
In one paragraph

Review in International journal of clinical pharmacy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

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.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
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

5 authors.

Rogério Caixinha AlgarvioFaculty of Sciences and Technology, University of Algarve, Faro, Portugal.ORCID http://orcid.org/0009-0005-8766-7450
Jaime ConceiçãoFaculty of Sciences and Technology, University of Algarve, Faro, Portugal.ORCID http://orcid.org/0000-0002-6201-3662
Pedro Pereira RodriguesRISE-Health, Department of Community Medicine, Information and Health Decision Sciences, Faculty of Medicine of the University of Porto, Porto, Portugal.ORCID http://orcid.org/0000-0001-7867-6682
Inês RibeiroRISE-Health, Department of Community Medicine, Information and Health Decision Sciences, Faculty of Medicine of the University of Porto, Porto, Portugal.ORCID http://orcid.org/0000-0002-3442-8158
Renato Ferreira-da-SilvaAlgarve Biomedical Centre Research Institute (ABC-Ri), University of Algarve, Faro, Portugal. renato.ivos@gmail.com.ORCID http://orcid.org/0000-0001-6517-6021

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPharmacovigilance is vital for monitoring adverse drug reactions (ADRs) and ensuring drug safety. Traditional methods are slow and inconsistent, but artificial intelligence (AI), through automation and advanced analytics, improves efficiency and accuracy in managing increasing data complexity.

aimTo explore AI's practical applications in pharmacovigilance, focusing on efficiency, process acceleration, and task automation. It also examines the use of an expert-defined Bayesian network for causality assessment in a Pharmacovigilance Centre, demonstrating its impact on decision-making.

methodA comprehensive literature narrative review was conducted in MEDLINE (via PubMed), Scopus, and Web of Science using a set of targeted keywords, including but not limited to "pharmacovigilance", "artificial intelligence", "adverse drug reactions" and "drug safety". Relevant studies were analysed without restrictions on publication year or language. The search was carried out in January 2025.

resultsAI has greatly improved pharmacovigilance by streamlining signal detection, surveillance, and ADR reporting automation. Techniques like data mining and automated signal detection have expedited safety signal identification, while duplicate detection has enhanced data precision in safety evaluations. AI has also refined real-world evidence analysis, deepening drug safety and efficacy insights. Predictive models now anticipate ADRs and drug-drug interactions, enabling proactive patient care. At a regional pharmacovigilance center, the implementation of an expert-defined Bayesian network has optimized causality assessment, reducing processing times from days to hours, minimizing subjectivity, and improving the reliability of drug safety evaluations.

conclusionAI holds significant promise for enhancing pharmacovigilance practices, yet its practical application remains primarily confined to academic research, with integration hindered by data quality issues, regulatory barriers, and the need for more transparent algorithms.

Indexed as

Adverse Drug Reaction Reporting SystemsArtificial IntelligenceDrug-Related Side Effects and Adverse ReactionsPharmacovigilanceBayes TheoremData MiningHumansArtificial intelligenceDrug-related side effects and adverse reactionsMachine learning data miningNatural language processingPharmacovigilance

Identifiers

PMID40736603
PMCPMC12335403

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.