Cited by 56Pharmacovigilance and Adverse Drug ReactionsPharmaceutical industry and healthcarePharmacogenetics and Drug Metabolism

FDA drug labeling: rich resources to facilitate precision medicine, drug safety, and regulatory science

Open access
Fang, Hong, Harris, Stephen C., Liu, Zhichao, Zhou, Guangxu, Zhang, Guoping, Xu, Joshua, Rosario, Lilliam, Howard, Paul C. +1 more·2016·Drug Discovery Today

Abstract

Here, we provide a concise overview of US Food and Drug Administration (FDA) drug labeling, which details drug products, drug-drug interactions, adverse drug reactions (ADRs), and more. Labeling data have been collected over several decades by the FDA and are an important resource for regulatory research and decision making. However, navigating through this data is challenging. To aid such navigation, the FDALabel database was developed, which contains a set of approximately 80000 labeling data. The full-text searching capability of FDALabel and querying based on any combination of specific sections, document types, market categories, market date, and other labeling information makes it a powerful and attractive tool for a variety of applications. Here, we illustrate the utility of FDALabel using case scenarios in pharmacogenomics biomarkers and ADR studies.

Integrity signals

Registry

Crossref · 10.1016/j.drudis.2016.06.006

Cites

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Claims the paper makes

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References 22 · Cited by 56

Authors
Fang, H., Harris, S. C., Liu, Z., Zhou, G., Zhang, G., Xu, J., Rosario, L., Howard, P. C., & Tong, W.
Affiliations
  • National Center for Toxicological Research (US)
  • United States Food and Drug Administration (US)
Corresponding author
Tong, Weida
Venue
Drug Discovery Today
Publisher
Elsevier BV
Published
2016-10
Volume
21
Issue
10
Pages
1566-1570
ISSN
1359-6446 (ISSN-L)
OpenAlex
W2422461554
Cited by
56
References
22
Citations by year
2026: 3 · 2025: 8 · 2024: 12 · 2023: 10 · 2022: 4 · 2021: 5 · 2020: 6 · 2019: 2 · 2018: 4 · 2017: 2
FWCI
2.17
Type
journal article
Language
en
Open access
Locations
  • Drug Discovery Today (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
Funders
  • FDA
  • Oak Ridge Institute for Science and Education
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Pharmacovigilance and Adverse Drug Reactions
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmaceutical industry and healthcare
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
Keywords
FDA drug labeling, drug-drug interactions, adverse drug reactions, drug safety, precision medicine, regulatory science, drug product information, full-text search
MeSH terms
Drug Labeling, United States, United States Food and Drug Administration, Databases, Factual, Internet, Precision Medicine, Drug-Related Side Effects and Adverse Reactions

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

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