Drug safety is a system of established principles and practical recommendations aimed at ensuring the safe and effective use of medicines. The aim of the study was to develop principles and design a conceptual model of drug safety based on a systematic analysis and an integrated approach. Material and methods. Systematic analysis of literary and Internet sources, a systematic approach, logical analysis, graphical method, modeling. Based on the study of the specifics of the existing pharmaceutical market and its participants, the regulatory framework, literary and Internet sources characterizing the circulation of medicines, drug-related problems of patient treatment, ethical norms and rules and system analysis, the principles of drug safety are proposed. The concept of drug safety is considered as a three-dimensional phenomenon requiring an integrated approach. Taking into account the system analysis, a conceptual model of drug safety has been developed, which includes 6 key elements: ensuring the safety of medicines from the state, manufacturers of medicines, medical and pharmaceutical workers, patients, the need for support and training of specialists, as well as directions for their implementation. The external factors influencing the clinical effectiveness of drugs and improving the quality of work of medical and pharmaceutical specialists are shown.
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