Author(s):
Vineetha Menon, Ahmed Mohamed Elgendy, Jisha Myalil Lucca
Email(s):
dr.vineetha@gmu.ac.ae
DOI:
10.52711/0974-360X.2026.00256
Address:
Vineetha Menon1*, Ahmed Mohamed Elgendy2, Jisha Myalil Lucca3
1Assistant Professor, Department of Pharmacy Practice, College of Pharmacy, Gulf Medical University, Ajman, United Arab Emirates.
2Postgraduate Research Student, Department of Pharmacy Practice, College of Pharmacy, Gulf Medical University, Ajman, United Arab Emirates.
3Assistant Professor, Department of Pharmacy Practice, College of Pharmacy, Gulf Medical University, Ajman, United Arab Emirates.
*Corresponding Author
Published In:
Volume - 19,
Issue - 4,
Year - 2026
ABSTRACT:
Introduction: Antithrombotic agents, including anticoagulants and antiplatelet drugs, are vital for preventing and managing thromboembolic events but pose risks of adverse drug reactions, drug-drug interactions, and dosing challenges. Limited real-world data from the United Arab Emirates warrant evaluation of prescribing and monitoring practices. This study aimed to assess prescribed daily doses of antithrombotic agents against World Health Organization-defined daily doses, evaluate related adverse drug reactions and drug-drug interactions, and analyze clinical outcomes. Methods: A prospective observational study was conducted over seven months at a private academic hospital in Ajman, United Arab Emirates. Adult inpatients receiving antithrombotic therapy were included. Data on demographics, medications, laboratory results, adverse drug reactions, and drug-drug interactions were collected. The World Health Organization Anatomical Therapeutic Chemical/Defined Daily Dose methodology was applied. Results: Of 130 patients screened, 100 were included. Antiplatelet drugs were prescribed to 67% and anticoagulants to 33%, with enoxaparin being the most frequent agent. Deviations from World Health Organization-defined daily doses were common, including overprescription of enoxaparin and aspirin and underdosing of apixaban. Adverse drug reactions occurred in 17% of patients, most commonly hematuria and thrombocytopenia; all were mild and 90% were preventable. Drug-drug interactions occurred in 10%, mainly pharmacodynamic, with 67% classified as major. Monitoring of coagulation parameters was inconsistent, with most patients not achieving therapeutic targets. Conclusion: The study revealed significant dosing variability, frequent adverse drug reactions and drug-drug interactions, and inadequate monitoring. Enhanced adherence to dosing guidelines and improved medication safety practices are essential to optimize outcomes in antithrombotic therapy.
Cite this article:
Vineetha Menon, Ahmed Mohamed Elgendy, Jisha Myalil Lucca. Drug Utilization, Safety, and Clinical Outcomes of Antithrombotic Agents: Insights from Real-World Hospital Data. doi: 10.52711/0974-360X.2026.00256
Cite(Electronic):
Vineetha Menon, Ahmed Mohamed Elgendy, Jisha Myalil Lucca. Drug Utilization, Safety, and Clinical Outcomes of Antithrombotic Agents: Insights from Real-World Hospital Data. doi: 10.52711/0974-360X.2026.00256 Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2026-19-4-45
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