jcm-logo

Journal Browser

Journal Browser

Clinical Advances in Drug Safety and Polypharmacy

A Special Issue of Journal of Clinical Medicine (ISSN 2077-0383) belonging to the section "Pharmacology".

Deadline for manuscript submissions: 20 November 2026 | Viewed by 1243

Editors


E-Mail Website
Guest Editor
Department of Neurosciences, Psychology, Drug Research and Child Health, Section of Pharmacology and Toxicology, University of Florence, 50141 Florence, Italy
Interests: pharmacovigilance; pharmacology; toxicology; pharmacoepidemiology; drug safety; clinical pharmacy; medical pharmacology
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
1. Department of Neurosciences, Psychology, Drug Research and Child Health, Section of Pharmacology and Toxicology, University of Florence, 50141 Florence, Italy
2. Tuscan Regional Centre of Pharmacovigilance, 50122 Florence, Italy
Interests: clinical pharmacology and toxicology; pharmacovigilance and pharmacoepidemiology; drug safety; clinical pharmacology
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Polypharmacy has become an increasingly prevalent phenomenon in modern healthcare, which has largely been driven by the global population aging, the rising burden of chronic diseases, and the growing complexity of therapeutic strategies. While the use of multiple medications is often necessary to achieve optimal disease management, it also introduces significant safety challenges. Polypharmacy is strongly associated with an increased risk of adverse drug reactions, drug–drug interactions, and reduced treatment adherence. These issues are particularly relevant in vulnerable populations such as older adults, patients with multiple comorbidities, and individuals receiving long-term or complex therapeutic regimens. Consequently, ensuring drug safety in the context of polypharmacy represents a critical priority for clinicians, researchers, and healthcare systems worldwide.

In recent years, advances in clinical pharmacology, pharmacovigilance, and real-world data analysis have presented new opportunities to better understand and mitigate medication-related risks. Emerging approaches such as personalized medicine, pharmacogenomics, clinical decision support systems, and structured deprescribing strategies are helping clinicians to balance the therapeutic benefits with potential harm. Moreover, the growing integration of artificial intelligence (AI) and machine learning into healthcare is creating new possibilities to improve medication safety. AI-based tools can support clinicians in identifying potential drug–drug interactions, predicting adverse drug reactions, analyzing large healthcare datasets, and optimizing prescribing practices in complex polypharmacy scenarios. In parallel, the increasing availability of real-world evidence from healthcare databases and pharmacovigilance systems is providing valuable insights into prescribing patterns, medication safety, and patient outcomes across diverse clinical settings. These developments highlight the urgent need for multidisciplinary research aimed at improving medication safety and optimizing therapeutic strategies in patients who are exposed to multiple treatments.

This Special Issue aims to present and disseminate the most recent advances related to drug safety and polypharmacy in clinical practice. We welcome contributions addressing pharmacological, clinical, epidemiological, and technological aspects that may improve the safe and rational use of medications in patients receiving multiple therapies. Submissions may include original research articles and literature reviews that provide novel insights into medication safety and optimization.

Topics of interest for publication include, but are not limited to, the following:

  • Adverse drug reactions associated with polypharmacy.
  • Drug–drug interactions and their clinical management.
  • Polypharmacy in multimorbid patients.
  • Deprescribing strategies and medication optimization.
  • Pharmacovigilance and real-world evidence in drug safety.
  • Artificial intelligence and machine learning applications in medication safety.
  • Medication adherence and patient-centered approaches.

Dr. Alfredo Vannacci
Dr. Giada Crescioli
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 250 words) can be sent to the Editorial Office for assessment.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-anonymized peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Journal of Clinical Medicine is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • polypharmacy
  • medication safety
  • adverse drug reactions
  • drug–drug interactions
  • pharmacovigilance
  • artificial intelligence in healthcare
  • precision medicine
  • deprescribing
  • pharmacoepidemiology

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • Reprint: MDPI Books provides the opportunity to republish successful Special Issues in book format, both online and in print.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

Jump to: Other

14 pages, 2171 KB  
Article
Drug Safety and Polypharmacy Signals in Ibrutinib-Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma: Age- and Sex-Specific FAERS Analysis of CYP3A Modifier and Antithrombotic Co-Exposure
by Velizar Shivarov
J. Clin. Med. 2026, 15(16), 6370; https://doi.org/10.3390/jcm15166370 - 18 Aug 2026
Viewed by 304
Abstract
Background/Objectives: Ibrutinib is an established treatment for chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), but its use commonly occurs in older patients with polypharmacy, cardiovascular comorbidity and infection vulnerability. CYP3A-modifying drugs and antithrombotic agents are clinically actionable co-exposure domains because they may alter ibrutinib [...] Read more.
Background/Objectives: Ibrutinib is an established treatment for chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), but its use commonly occurs in older patients with polypharmacy, cardiovascular comorbidity and infection vulnerability. CYP3A-modifying drugs and antithrombotic agents are clinically actionable co-exposure domains because they may alter ibrutinib exposure, bleeding risk or the management of atrial arrhythmia. This study evaluated post-marketing reporting patterns for these co-exposures in FAERS. Methods: Adult FAERS reports through 25Q2 with ibrutinib exposure and CLL/SLL-compatible indications were analyzed after false-positive indication captures were removed. Co-exposures were defined at report level using prespecified drug dictionaries, and grouped adverse-event reporting was evaluated using reporting odds ratio, proportional reporting ratio, chi-square and an information-component-style two-by-two metric. Results: The final cohort comprised 20,878 adult CLL/SLL + ibrutinib reports. CYP3A modifier co-exposure was present in 1373 reports (6.6%), and antithrombotic co-exposure in 3701 reports (17.7%). Antithrombotic exposure increased with age, from 9.8% in reports aged 18–64 years to 23.2% in reports aged ≥75 years. CYP3A modifier exposure was associated with enriched reporting of infection and cytopenia phenotypes, particularly severe infection-like events with CYP3A inhibitors and inducers. Antithrombotic exposure showed consistent reporting enrichment for atrial arrhythmia, bleeding and major bleeding-like events, with the strongest grouped signals among anticoagulant-exposed reports. Overlap analyses showed that the co-exposure domains were not mutually exclusive. Conclusions: These findings should be interpreted as reporting disproportionality rather than incidence or causal risk, but they support prioritizing CYP3A-modifying drugs and antithrombotic therapy during medication reconciliation, interaction screening and risk mitigation in older patients receiving ibrutinib. Full article
(This article belongs to the Special Issue Clinical Advances in Drug Safety and Polypharmacy)
Show Figures

Figure 1

Other

Jump to: Research

11 pages, 259 KB  
Perspective
Renal Dose Adjustment in European Primary Care: Clinical Nuances and Practical Challenges
by Anna Maria Dworakowska, Jolanta Małyszko and Magdalena Bujalska-Zadrożny
J. Clin. Med. 2026, 15(12), 4737; https://doi.org/10.3390/jcm15124737 - 18 Jun 2026
Viewed by 555
Abstract
Appropriate dose adjustment of renally eliminated medicines is central to safe pharmacotherapy in patients with chronic kidney disease; yet, in European primary care, it is systematically undermined not by lack of knowledge, but by structural misalignment between laboratory reporting, regulatory product information, and [...] Read more.
Appropriate dose adjustment of renally eliminated medicines is central to safe pharmacotherapy in patients with chronic kidney disease; yet, in European primary care, it is systematically undermined not by lack of knowledge, but by structural misalignment between laboratory reporting, regulatory product information, and clinical guidelines. This Perspective argues that the core barrier to optimal renal dose adjustment is a mismatch between routinely reported indexed eGFR and dosing requirements based on absolute renal function, compounded by persistent regulatory reliance on the Cockcroft–Gault equation despite its known limitations. We show how these structural inconsistencies, together with patient-related factors such as frailty, ageing, and body size, generate uncertainty at the point of prescribing and contribute to persistent variability in dosing decisions. To address this challenge, we propose a structured, context-aware renal dosing framework designed for routine primary care. The framework integrates regulatory guidance, multiple methods of renal function estimation, and patient-specific modifiers into a stepwise decision process. Clinical vignettes illustrate how divergent renal function estimates and regulatory requirements can lead to different dosing decisions in everyday practice. By reframing renal dose adjustment as a context-driven clinical process rather than a purely equation-based task, this Perspective highlights the need for regulatory alignment and pragmatic decision tools to improve prescribing quality in patients with chronic kidney disease. Full article
(This article belongs to the Special Issue Clinical Advances in Drug Safety and Polypharmacy)
Back to TopTop