Background: The drug information most commonly requested by patients is to learn more about potential adverse drug reactions (ADRs) of their drugs. Such information should be customizable to individual information needs. While approaches to automatically aggregate ADRs by text-mining processes and establishment of respective databases are well known, further efforts to map additional ADR information are sparse, yet crucial for customization. In a proof-of-principle (PoP) study, we developed a database format demonstrating that natural language processing can further structure ADR information in a way that facilitates customization.
Methods: We developed the database in a 3-step process: (1) initial ADR extraction, (2) mapping of additional ADR information, and (3) review process. ADRs of 10 frequently prescribed active ingredients were initially extracted from their Summary of Product Characteristics (SmPC) by text-mining processes and mapped to Medical Dictionary for Regulatory Activities (MedDRA) terms. To further structure ADR information, we mapped 7 additional ADR characteristics (i.e. frequency, organ class, seriousness, lay perceptibility, onset, duration, and management strategies) to individual ADRs. In a PoP study, the process steps were assessed and tested. Initial ADR extraction was assessed by measuring precision, recall, and F-scores (i.e. harmonic mean of precision and recall). Mapping of additional ADR information was assessed considering pre-defined parameters (i.e. correctness, errors, and misses) regarding the mapped ADR characteristics.
Results: Overall the SmPCs listed 393 ADRs with an average of 39.3 ± 18.1 ADRs per SmPC. For initial ADR extraction precision was 97.9% and recall was 93.2% leading to an F-score of 95.5%. Regarding mapping of additional ADR information, the frequency information of 28.6 ± 18.4 ADRs for each SmPC was correctly mapped (72.8%). Overall 77 ADRs (20.6%) of the correctly extracted ADRs did not have a concise frequency stated in the SmPC and were consequently mapped with 'frequency not known'. Mapping of remaining ADR characteristics did not result in noteworthy errors or misses.
Conclusion: ADR information can be automatically extracted and mapped to corresponding MedDRA terms. Additionally, ADR information can be further structured considering additional ADR characteristics to facilitate customization to individual patient needs.
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http://dx.doi.org/10.1016/j.ijmedinf.2019.103970 | DOI Listing |
J Ethnopharmacol
January 2025
Henan University of Chinese Medicine, 156 Jinshui East Road, Zhengzhou, 450046, China; The Engineering and Technology Center for Chinese Medicine Development of Henan Province, 156 Jinshui East Road, Zhengzhou, 450046, China. Electronic address:
Ethnopharmacological Relevance: The Chinese herbal Plantaginis Herba (PL) is one of the most widely used plants for both medicinal and dietary purposes. Plantaginis Herba is the main medicine used in a traditional Chinese prescription called Cheqiancao decoction, and it is known for its liver and kidney protective properties.
Aim Of The Study: The aim of the present study was to explore the interventions and mechanisms of PL in ADR nephropathy by performing an integrated analysis of in vitro and in vivo experiments.
Introduction: This study aims to explore the reno-protective effect of Curcumin in focal and segmental glomerulosclerosis (FSGS) in Murine models, a common chronic glomerulopathy that leads to end stage renal disease.
Methods: Adult Wistar rats were used in this experiment. One group was treated with intravenous Adriamycin (ADR) injection to induce FSGS similar to that seen in humans and a second group was co-administered ADR and Curcumin (ADR-CUR).
Pharmaceuticals (Basel)
December 2024
Clinical Pharmacology and Pharmacotherapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000 Leuven, Belgium.
Background/objectives: While breastfeeding is highly recommended, breastfed infants may be exposed to drugs by milk due to maternal pharmacotherapy, resulting in a risk of adverse drug events (ADE) or reactions (ADRs). The U.S.
View Article and Find Full Text PDFFront Pharmacol
December 2024
Service of Clinical Pharmacology, Hospital Universitari Germans Trias i Pujol, Barcelona, Spain.
Objectives: We aimed to assess the characteristics of adverse drug reactions (ADRs) collected in a university hospital.
Methods: A retrospective analysis of ADRs spontaneously reported in the Hospital Pharmacovigilance Program database (RutiRAM) over a 13-year period was conducted. The analysis included a description of ADRs [System Organ Class (SOC)] and their seriousness, the drugs involved [level 1 of the Anatomical Therapeutic Chemical (ATC) Classification System], drug-drug interactions, medication errors, drugs 'under additional monitoring', positive rechallenge, and the 'pharmacovigilance interest' of ADRs.
Arch Orthop Trauma Surg
December 2024
School of Medicine and Health Sciences, Division of Orthopaedics at Campus Pius-Hospital, Carl von Ossietzky Universität Oldenburg, Georgstraße 12, 26121, Oldenburg, Germany.
Introduction: Periprosthetic joint infection (PJI) is a serious complication following primary total joint arthroplasty (TJA). PJI accounts for 15-25% of revision surgeries, therefore it is associated with PJI is associated with substantial patient morbidity and mortality as well as increased healthcare expenditures due to complex treatment strategies. Recently, intraoperative local application of vancomycin powder is increasingly being used in primary total hip and knee arthroplasty (THA, TKA) as an additive strategy for PJI prevention.
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