Приостановлено применение двух серий офтальмологического анестетика
Федеральная служба по надзору в сфере здравоохранения сообщает о решении производителя приостановить применение двух серий препарата «Оксибупрокаин». Информационное письмо об этом опубликовано на сайте ведомства 3 мая.
Речь идёт о препарате «Оксибупрокаин, капли глазные, 0,4 % 5 мл, флаконы-капельницы (1), пачки картонные» серий 10622, 20922 производства ФГУП «Московский эндокринный завод». Причиной для приостановления применения является развитие нежелательной реакции на фоне использования препарата.
Напомним, что согласно пункту 30 приказа № 646н «О правилах надлежащей практики хранения и перевозки ЛС» лекарственные препараты, обращение которых приостановлено, должны быть изолированы и помещены в карантинную зону хранения, чтобы исключить их дальнейший оборот. Это касается всех субъектов обращения ЛС, в том числе аптек и медицинских учреждений.
«Катрен-Стиль» ежемесячно составляет перечень лекарственных средств, оборот которых был прекращён Росздравнадзором или производителем, а также препаратов, которые были отозваны производителями или лишены государственной регистрации. Последний обзор информационных писем регулятора со списком таких ЛС читайте по этой ссылке.
В октябре прошлого года Минздрав увеличил количество причин, по которым может быть приостановлено применение ЛС на территории России.
4 мая 2023
Фото: © evrim ertik (istockphoto.com
Выпуск: №233, май 20231986 просмотров
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