Катрен Стиль
Минздрав отменил государственную регистрацию одной из лекарственных форм «Тамифлю»
Министерство здравоохранения приняло решение отменить государственную регистрацию и исключить из Государственного реестра лекарственных средств для медицинского применения препарат «Тамифлю» (МНН: осельтамивир) в форме порошка для приготовления суспензии для приема внутрь. Соответствующая информация была опубликована в Государственном реестре лекарственных средств 9 января 2017 г.
Регистрация была отменена на основании заявления, поданного российским представительством производителя лекарства, компанией Рош (Roche Holding AG). Это связано с тем, что «Тамифлю» больше не производится именно в этой лекарственной форме. Срок годности последней ввезенной в Россию серии истек в августе 2016 года. В настоящее время препарат имеет регистрацию на территории РФ в лекарственной форме «капсулы».
Осельтамивир, выпускаемый в форме порошка для суспензии и капсул, включен в Перечень жизненно необходимых и важнейших лекарственных препаратов, а также в минимальный ассортимент лекарственных препаратов, необходимых для оказания медицинской помощи.
Согласно Государственному реестру лекарственных средств «Тамифлю» был единственным препаратом, содержащим осельтамивир и выпускающимся в форме порошка для приготовления суспензии для приема внутрь.
Источники:
Государственный реестр лекарственных средств (PDF)Распоряжение Правительства РФ от 26.12.2015 N 2724-р (Об утверждении перечней ЖНВЛП и минимального ассортимента для аптек) (PDF)
11 января 2017
Фото: www.istockphoto.com/KatarzynaBialasiewicz
Выпуск: №156, январь 20171466 просмотров
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