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FDA Adverse Event Reporting System (FAERS) Essentials: A Guide to Understanding, Applying, and Interpreting Adverse Event Data Reported to FAERS

Clinical Pharmacology & Therapeutics(2025)10.1002/cpt.3701Source: DataRank Database

FDA Adverse Event Reporting System (FAERS) Essentials: A Guide to Understanding, Applying, and Interpreting Adverse Event Data Reported to FAERS is a research paper published in Clinical Pharmacology & Therapeutics (2025). On theSindex it has a DataRank of 0. It has been cited 86 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access86 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (1 grants)Impact (FWCI 64.29)OA: greenTopics (24)IDs (PubMed, PMC, OpenAlex)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (4)

Melissa Reyes ORCID,Jennifer L. Greene-Naples ORCID,Gerald J. Dal Pan ORCID,E. Lake Potter ORCID

Live enrichment

PubMed:40384638 PMC:PMC12393772 OpenAlex:https://openalex.org/W4410481172

Intramural FDA HHS

Grant: FD999999

FWCI

64.29

Citation Percentile

1.0%

Citation Trend

2025

2026

greenLicense: public-domain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/12393772

publisherhttps://ascpt.onlinelibrary.wiley.com/doi/pdf/10.1002/cpt.3701

journalhttps://doi.org/10.1002/cpt.3701

repositoryhttps://pubmed.ncbi.nlm.nih.gov/40384638

Fields of Study

Pharmacovigilance and Adverse Drug ReactionsPharmaceutical studies and practicesStatistical Methods in Clinical TrialsHumansAdverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse ReactionsProduct Surveillance, PostmarketingUnited StatesUnited States Food and Drug Administration

MeSH Terms

HumansProduct Surveillance, PostmarketingUnited StatesUnited States Food and Drug AdministrationAdverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse Reactions

Keywords

Adverse Event Reporting SystemAdverse effectPostmarketing surveillanceMedicineEvent (particle physics)Food and drug administrationPharmacovigilanceComputer sciencePharmacology

Sustainable Development Goals

SDG 0: Responsible consumption and productionSDG 0: Zero hunger