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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">vedomostiregmed</journal-id><journal-title-group><journal-title xml:lang="ru">Регуляторные исследования и экспертиза лекарственных средств</journal-title><trans-title-group xml:lang="en"><trans-title>Regulatory Research and Medicine Evaluation</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">3034-3062</issn><issn pub-type="epub">3034-3453</issn><publisher><publisher-name>Federal State Budgetary Institution ‘Scientific Centre for Expert Evaluation of Medicinal Products’ of the Ministry of Health of the Russian Federation (FSBI ‘SCEEMP’)</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">vedomostiregmed-144</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Римские критерии IV функциональных заболеваний желудочно-кишечного тракта в оценке взаимозаменяемости лекарственных препаратов: взгляд врача - клинического фармаколога</article-title><trans-title-group xml:lang="en"><trans-title>Rome IV criteria of functional gastrointestinal diseases in evaluation of drugs interchangeability: through the eyes of a clinical pharmacologist</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Сереброва</surname><given-names>С. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Serebrova</surname><given-names>S. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Прокофьев</surname><given-names>А. Б.</given-names></name><name name-style="western" xml:lang="en"><surname>Prokofiev</surname><given-names>A. B.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Журавлева</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Zhuravleva</surname><given-names>M. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Еременко</surname><given-names>Н. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Eremenko</surname><given-names>N. N.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Научный центр экспертизы средств медицинского применения</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Scientific Centre for Expert Evaluation of Medicinal Products</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2017</year></pub-date><pub-date pub-type="epub"><day>13</day><month>02</month><year>2018</year></pub-date><volume>7</volume><issue>4</issue><fpage>221</fpage><lpage>227</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Сереброва С.Ю., Прокофьев А.Б., Журавлева М.В., Еременко Н.Н., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Сереброва С.Ю., Прокофьев А.Б., Журавлева М.В., Еременко Н.Н.</copyright-holder><copyright-holder xml:lang="en">Serebrova S.Y., Prokofiev A.B., Zhuravleva M.V., Eremenko N.N.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.vedomostincesmp.ru/jour/article/view/144">https://www.vedomostincesmp.ru/jour/article/view/144</self-uri><abstract><p>Проанализированы факторы, приводящие к утрате взаимозаменяемости воспроизведенных лекарственных препаратов у пациентов с функциональными расстройствами желудочно-кишечного тракта (ФР ЖКТ). Обоснована актуальность обновления законодательной базы и государственного регулирования обращения воспроизведенных лекарственных препаратов в Российской Федерации. На основании представленной современной классификации ФР ЖКТ, согласно Римским критериям IV, выявлены проблемные аспекты надежности неадаптивных оценочных признаков взаимозаменяемости воспроизведенных лекарственных препаратов. В статье подробно рассмотрены генетически детерминированные различия функциональной активности желудка и кишечника у здоровых людей и пациентов с ФР ЖКТ, которые не позволяют переносить уже установленную взаимозаменяемость на популяцию больных с ФР ЖКТ. Также отмечается возможность взаимодействия лекарственных препаратов, применяемых пациентами с ФР ЖКТ по прямым показаниям или для лечения сопутствующих заболеваний. Доказано, что Римские критерии IV могут ограниченно применяться в исследованиях терапевтической эквивалентности воспроизведенных лекарственных препаратов при функциональных расстройствах желудочно-кишечного тракта как по прямым показаниям, так и при сопутствующей терапии.</p></abstract><trans-abstract xml:lang="en"><p>The article analyses the factors likely leading to the lack of interchangeability of generic drugs for patients with functional gastrointestinal disorders (FGID). It substantiates the need for improvement of the legal basis and regulatory framework underlying drugs circulation in the Russia. Based on the modern classification of FGIDs, laid down in the article, and according to Rome IV criteria the authors formulated major concerns related to the reliability of non-adaptive assessment parameters of generics interchangeability. The article looks into genetically determined differences in the functional activity of the stomach and bowel in healthy people and people with FGIDs that preclude extrapolation of already established interchangeability to the population of patients with FGIDs. The article also highlights potential interaction of drugs that are prescribed to patients with FGIDs either for the treatment of the underlying disease or co-morbidities. It was shown that Rome IV criteria can be used (to a limited extent) in therapeutic equivalence studies of generic drugs used either as primary or concomitant medications in patients with FGIDs.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>функциональные расстройства</kwd><kwd>Римские критерии IV</kwd><kwd>взаимозаменяемость</kwd><kwd>воспроизведенные лекарственные средства</kwd><kwd>синдром раздраженной кишки</kwd><kwd>functional disorders</kwd><kwd>Rome IV criteria</kwd><kwd>interchangeability</kwd><kwd>generic drugs</kwd><kwd>irritable bowel syndrome</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Федеральный закон Российской Федерации от 12 апреля 2010 г. № 61-ФЗ «Об обращении лекарственных средств». 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