EDITORIAL
REVIEWS AND ORIGINAL ARTICLES
This review presents information on pharmaceuticals that have the properties of inverse agonists. The article describes the features of the interaction of the ligand - receptor with constitutive conformational changes. Many of ligands, assumed to be neutral antagonists, behave as inverse agonists displaying negative efficacy in experimental systems. This suggests that their therapeutic actions may involve not only receptor blockade, but also the decrease of spontaneous receptor activity. Examples of inverse agonists that influence the processes of excitation of adrenergic, histaminergic, opioid and benzodiazepine receptors are presented. The existence of constitutive activity in vivo and its pathophysiological relevance are also discussed
This review presents information on pharmaceuticals that have the properties of inverse agonists. The article describes the features of the interaction of the ligand - receptor with constitutive conformational changes. Many of ligands, assumed to be neutral antagonists, behave as inverse agonists displaying negative efficacy in experimental systems. This suggests that their therapeutic actions may involve not only receptor blockade, but also the decrease of spontaneous receptor activity. Examples of inverse agonists that influence the processes of excitation of adrenergic, histaminergic, opioid and benzodiazepine receptors are presented. The existence of constitutive activity in vivo and its pathophysiological relevance are also discussed
This article describes herpes zoster (HZ) manifestation in RA patient treated with Methotrexate (MTX). The possibility of effective continuation of MTX therapy after the symptoms of HZ resolve is demonstrated. The possibility of a causal relationshi p between the use of the MT and the manifestation HZ infection, and treatment options are discussed
The article presents the results of a comparative analysis of Good
pharmacovigilance practices (GVP), developed by experts of the regulatory bodies
of the European Union (EU) and the United States. It is shown that the EU GVP cover almost all possible aspects of pharmacovigilance. It is noted that the disadvantages of EU GVP are difficulties in the correct understanding and interpretation of certain definitions and processes, as well as the complexity of the implementation in practice of a number of provisions, mainly related to the organization of the quality management system, including audit and inspection. As the basis for development of the Russian Rules GVP is recommended to use the GVP EU
In article results pharmacoepidemiology researches on studying of knowledge of pharmacists (n=187) on safety issues medicinal and pharmacovigilance are resulted. 28 % of pharmacists have adverse drug reactions to medicines in the practice, however submit spontaneous messages only 5 % of respondents. Princi pal causes of low activity of pharmacists - a lack of time for drawing up of reports and low level of knowledge in the field of safety of medical products. 89 % of pharmacists need educational programs on pharmacovigilance
RELEVANT INFORMATION
ISSN 2619-1164 (Online)