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Analysis and mining of adverse events associated with vorapaxar: A FAERS database-based study
published 13 Feb 2026
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Safety population size and duration of exposure prior to approval of new medicines: A database analysis of medicines centralised approved in the European Union between 2011 and 2023
published 09 Feb 2026
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Disproportionality analysis of drug-associated progressive multifocal leukoencephalopathy using spontaneous reports: A 20-year signal detection study based on the FAERS database
published 03 Feb 2026
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Systematic analysis of proton pump inhibitors-related adverse reactions using the FDA adverse event reporting system database
published 02 Feb 2026
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An interpretable machine learning framework for adverse drug reaction prediction from drug-target interactions
published 30 Jan 2026
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Exploring adverse events associated with vosoritide monotherapy: Insights from the FDA Adverse Event Reporting System
published 29 Jan 2026
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SmUDo (Smart Unit-Dose): Redefining efficiency, quality, and staffing strategies for optimized processes
published 16 Jan 2026
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Endocrine advantages of PD-1/PD-L1 therapy: Comparative analysis of FAERS-JADER
published 09 Jan 2026
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Suicide adverse events associated with zopiclone and eszopiclone: A pharmacovigilance analysis based on FAERS, JADER and CVARD
published 08 Jan 2026
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Adverse events associated with cyclophosphamide: A pharmacovigilance study using the FDA adverse event reporting system
published 06 Jan 2026
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Collaborative and co-Ordinated action for Medication Safety (COMS): Experience-based co-design of an intervention blueprint to improve general practice and community pharmacy collaboration
published 26 Dec 2025
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Patient safety risk associated with synchronous telehealth: A scoping review
published 16 Dec 2025
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Safety profile of TNF- alpha Inhibitors in pediatric patients: A post-marketing surveillance study based on the FAERS database
published 02 Dec 2025
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