Тагамет инструкция по применению

Препарат представляет собой антисекреторное противоязвенное лекарственное средство.Тагамет представляет собой антисекреторное противоязвенное лекарственное средство, Н2-блокатор рецепторов гистаминовых. Назначается при изжоге и ряде заболеваний, ее вызывающих.

Способствует уменьшению пептической активности сока желудочного и секреции в желудке соляной кислоты. Ускоряет процессы заживления и грануляции.

Вещества, входящие в состав препарата Тагамет, проникают в организм и всасываются из ЖКТ. Спустя несколько часов, концентрация данных компонентов в крови достигает своего максимального значения.

Содержание[Скрыть]

    • 1. Инструкция по применению
    • 2. Побочные действия
    • 3. Условия и сроки хранения
    • 4. Цена
    • 5. Аналоги
    • 6. Отзывы
    • 7. Итог

1. Инструкция по применению

Фармакологическое действие

Медикамент является антисекреторным противоязвенным лекарственным препаратом, Н2-блокатором гистаминовых рецепторов. Применяется для лечения людей с изжогой и некоторыми вызывающими ее заболеваниями. Уменьшает выработку соляной кислоты в желудке, а также пептическую активность желудочного сока. Ускоряет процессы грануляции, заживления.

Находящиеся в Тагамете компоненты попадают в организм, всасываются из ЖКТ. По прошествии нескольких часов их содержание в крови становится максимальным.

Показания к применению

Тагамет принимают при:

  • Медикамент используются при изжоге и некоторых заболеваниях, которые ее вызывают.язвенной болезни кишки 12-перстной, желудка;
  • профилактике и лечении повреждений слизистой ЖКТ язвенных (в том числе лекарственных и стрессовых);
  • рецидивирующих послеоперационных язвах;
  • изжоге, которая связана с гиперхлоргидрией;
  • рефлюкс-эзофагите;
  • системном мастоцитозе;
  • Золлингера-Эллисона синдроме;
  • эрозивном гастрите;
  • полиэндокринном аденоматозе;
  • профилактике пневмонита аспирационного;
  • кровотечениях из отделов ЖКТ верхних (в том числе послеоперационных).

Также Тагамет назначают в качестве вспомогательной терапии: при ревматоидном артрите, недостаточности ферментов железы поджелудочной, острой форме крапивницы.

Способ применения

Существует 3 способа применения Тагамета: перорально (в процессе приема пищи либо до него), в/в и в/м. При обострении язвенной болезни 12-перстной кишки и желудка у взрослых пациентов препарат назначают внутрь. Суточная доза составляет 800 мг, принимаемых в 1 прием ежедневно (перед сном).

Выписывается по рецепту врача, лечебный курс проходит исключительно под его наблюдением.Также допускается применение лекарства в следующих дозах:

  • дважды в день по 400 мг (во время утреннего приема пищи и перед сном);
  • трижды в сутки по 200 мг и дополнительно 400 мг вечером, перед сном (всего 1 г в день).

Максимальная суточная доза составляет 2,4 г. Известны случаи, когда пациентам, страдающим патологическими гиперсекреторными состояниями, назначали до 12 г в сутки.

Первоначальный курс лечения составляет не менее четырех недель. Терапия при язвенной болезни желудка продолжается на протяжении шести недель.

Для профилактики обострений язвенной болезни 12-перстной кишки и желудка назначают пероральное применение препарата, по 400 мг перед сном.

Порядок лечения других заболеваний:

  • Рефлюкс-эзофагит: внутрь, четырежды в сутки по 400 мг. Препарат принимают во время еды и перед отходом ко сну. Продолжительность терапии составляет от 28 до 56 дней (4-8 недель).
  • Наличие кровотечений в верхних отделах ЖКТ: 8-10 раз в день по 200 мг внутривенно (суточная доза составляет 1,6-2 г).
  • Лечение стрессовых повреждений слизистой верхних отделов ЖКТ: инфузионно или в/в медленно, от пяти до десяти раз в день по 200 мг (скорость инфузии максимальная составляет 150 мг в час). Также препарат можно принимать внутрь, каждые четыре-шесть часов по 200-400 мг.
  • Профилактика пневмонита аспирационного: внутримышечно. За час до общей анестезии вводят 300 мг, а затем – по 0,3 г в/в либо в/м каждые четыре часа вплоть до выхода из анестезии.
  • Синдром Золлингера-Эллисона, прочие гиперсекреторные состояния: в суточной дозе от 1,6 до 2 г в несколько приемов.
  • Нарушение почечной функции: внутрь, суточная доза зависит от КК. Для КК от 30 до 50 мл/мин – 0,8 г, для КК от 15 до 30 мл/мин – 0,6 г, для КК 0-15 мл/мин – 0,4 г. Либо внутривенно, каждые двенадцать часов по 300 мг (при необходимости дозу, равную 300 мг, можно вводить каждые восемь часов или чаще). Если имеется сопутствующее нарушение печеночной функции, может потребоваться уменьшение дозы.
  • Крапивница (вспомогательное лечение): внутривенно, на протяжении 15-20 минут 300 мг.

Детям препарат назначают следующим образом:

  • Язвенная болезнь желудка, 12-перстной кишки: внутрь. Суточная доза – от 20 до 40 мг на один килограмм веса, разделенных на 4 приема. Лекарство принимают перед сном и во время еды.
  • Гастроэзофагеальный рефлюкс: по 40-80 мг (суточная доза) на килограмм веса в 4 приема.

Также препарат может вводиться в/в, в/м, каждые шесть-восемь часов по 5-10 мг/кг (при внутривенном введении средство разбавляется совместимым раствором до нужного объема и вводится не менее 15-20 минут при инфузии и не менее 2 минут при инъекции).

При нарушении почечной функции суточная доза на килограмм веса снижается, а интервал между введениями увеличивается.

Форма выпуска, состав

Тагамет продается в виде раствора для в/м, в/в введения, а также в виде белых таблеток несколько выпуклой или круглой формы. Активным действующим ингредиентом препарата является вещество под названием «циметидин».

Циметидин (Tagamet) блокирует выделение желудочного сока и применяется при лечении язвенной болезни и повышенной кислотности.

Циметидин (Tagamet) блокирует выделение желудочного сока и применяется при лечении язвенной болезни и повышенной кислотности.

Взаимодействие с другими препаратами

Тагамет увеличивает эффект БМКК и м-холиноблокаторов, а также выраженность побочных действий опиоидных анальгетиков.

Снижает абсорбцию хлорпромазина, эффект кетоконазола, андрогенов и барбитуратов (взаимно).

Способствует снижению печеночного клиренса лидокаина (необходима скорректировать режим дозирования).

Не рекомендуется совместное применение лекарств, вызывающих нейтропению (в т.ч. цитостатиков).

Метоклопрамид и антациды способствуют уменьшению всасывания.

2. Побочные действия

Возможные побочные реакции
Тракт пищеварительный тошнота, диарея, сухость во рту, уменьшение всасывания витамина B12, рвота, метеоризм; при внезапной отмене препарата – рецидив язвенной болезни. В ряде случаев увеличивается активность трансаминаз «печеночных».
Нервная система сонливость, парестезии, галлюцинации, повышенная утомляемость, головокружение, депрессия, спутанность сознания (обычно у пациентов, страдающих нарушениями печеночной/почечной функции).
Мочеполовая система нефрит интерстициальный (повышение мочевины концентрации, гиперкреатининемия), снижение потенции, отеки.
Органы кроветворения тромбоцитопения, панцитопения, лейкопения, апластическая анемия, агранулоцитоз.
Реакции аллергического характера зуд, ангионевротический отек, кожные высыпания, гиперемия.
Иные гиперпролактинемия, снижение концентрации паратгормона, артралгия, алопеция, иммунодепрессия, гинекомастия, миалгия, ксеродермия.

Передозировка

Сопровождается тревожностью, брадикардией, угнетением дыхательного центра, иногда – сухостью во рту, тахикардией.

В течение первых 4 часов после приема таблетки следует промыть желудок. Если есть необходимость, врач проводит гемодиализ, назначает симптоматическую терапию, устанавливает наблюдение за пациентом.

Противопоказания

Запрещено принимать Тагамет при:

  • нейтропении;
  • недостаточности печеночной/почечной;
  • гиперчувствительности;
  • лактации, беременности.

С осторожностью применяют в детском возрасте (менее 16 лет), а также при:

  1. циррозе печени (если в анамнезе имеется портосистемная энцефалопатия);
  2. ХСН;
  3. заболеваниях органов кроветворения.

При беременности

Противопоказано.

Особые указания

  • Составляя схему лечения пожилого человека, нужно учитывать состояние ССС и почечного аппарата.
  • Использование Тагамета у людей с ИВЛ чревато ростом некоторых микроорганизмов в содержимом желудка. Данные микроорганизмы способны вызывать инфекции дыхательных путей и пневмонию.
  • Нередко лечение маскирует симптомы и вызывает временное улучшение самочувствия у людей, страдающих раком желудка.
  • Принимать блокаторы H2-гистаминовых рецепторов необходимо, когда с момента приема кетоконазола или итраконазола пройдет два часа. Это позволяет предотвратить уменьшение их всасывания.
  • Отмена Тагамета проводится постепенно.
  • Гинекомастия при прекращении лечения обратима практически всегда.
  • При длительной терапии нужно контролировать показатели периферической крови, а также функции почек и печени.
  • Некоторые напитки, лекарства и продукты питания способны раздражать слизистую оболочку желудка. Употреблять их во время терапии не рекомендуется.
  • Тагамет способен подавлять реакцию кожи на гистамин, приводя к ложноотрицательным результатам.
  • Тагамет может противодействовать влиянию гистамина и пентагастрина на кислотообразующую желудочную функцию. Принимать его в течение суток, предшествующих тесту, не рекомендуется.

Влияние на способность к вождению автотранспорта, управлению механизмами

Детям, подросткам, также женщинам в периоды беременности и лактации продукт назначают только по строгим показаниям.

Неизвестно, как влияет Тагамет на способность управлять транспортом и прочими механизмами. Однако во время лечения могут возникать периодические головокружения, что непременно нужно учитывать.

Беременность и лактация

В данные периоды (лактация, беременность) Тагамет не применяют.

Применение в педиатрии

Лекарство противопоказано лицам до 14 лет.

При нарушенной функции почек

При почечной недостаточности медикамент не назначают. Дозу для людей с нарушенной почечной функцией нужно подбирать, основываясь на значениях клиренса креатинина. Если человек находится на гемодиализе, препарат назначают по окончании процедуры. Это связано с тем, что циметидин при гемодиализе выводится из организма.

При нарушенной функции печени

При печеночной недостаточности Тагамет не применяют.

Условия продажи в аптеках

Для покупки лекарства в аптеке нужно обзавестись рецептом доктора.

3. Условия и сроки хранения

Тагамет хранят в месте, защищенном от повышенной влажности и света, при температуре, которая варьируется от 15 до 25 градусов.

4. Цена

Средняя цена в России

В настоящее время действие разрешения на применение Тагамета на территории РФ закончилось.

Средняя стоимость в Украине

Упаковка Тагамета обходится жителям Украины примерно в 40 гривен.

Видео на тему: Tagamet ‘Future’ Commercial Dir:Simon Gargette

5. Аналоги

Препарат Тагамет имеет большое число аналогов, в частности: Цинамет; Циметидин; Цемидин; Примамет; Улкузал; Йенаметидин; Ново-Циметин; Беломет; Альтрамет; Ало-Циметидин.

  • Если у вас появились какие-то симптомы заболевания необходимо срочно обратиться к врачу. Посмотреть список гастроэнтерологических клиник можно у нас на сайте https://gastrocure.net/kliniki.html
  • Вам будет интересно! В статье описаны симптомы, дающие возможность заподозрить на ранних стадиях наличие заболеваний печени https://gastrocure.net/bolezni/gepatit.html
  • Также вам будет интересно узнать побольше про лечение разных заболеваниях желудочно-кишечного тракта https://gastrocure.net/bolezni.html

6. Отзывы

В связи с тем, что разрешение на продажу препарата на территории РФ истекло, отзывы о лекарственном средстве найти достаточно трудно.

Пациенты, которым удалось испробовать на себе действие Тагомета, говорят о данном ЛС в положительном ключе.

Ознакомиться с отзывами пациентов о препарате можно в конце статьи.

7. Итог

  1. Выбирая режим дозирования для пенсионеров нужно учитывать состояние ССС и функции почек.
  2. У лиц, страдающих онкологией желудка, лечение может скрывать симптомы болезни, вызывая временное улучшение состояния.
  3. Применение препарата у лиц с ИВЛ может стать причиной роста в желудке микроорганизмов, способных вызывать пневмонию и прочие инфекционные недуги дыхательных путей.
  4. Во время терапии желательно отказаться от употребления напитков и пищи, способных раздражать слизистую оболочку желудка.
  5. Таким образом, Тагамет позиционируется как эффективный противоязвенный препарат. Из аптек отпускается исключительно по рецепту врача, а процесс лечения проходит строго под наблюдением специалиста.

Гастроэнтеролог, Терапевт

Врач проводит общую диагностику внутренних органов. Делает заключения о нарушениях в ЖКТ по результатам проведенного обследования и назначает соответствующее лечение. Среди диагнозов, которыми занимается специалист: язва желудка и 12-ти перстной кишки, гастрит, дисбактериоз и т.д.Другие авторы

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    cimetidine will increase the level or effect of darifenacin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • darolutamide

    darolutamide will increase the level or effect of cimetidine by Other (see comment). Avoid or Use Alternate Drug. Darolutamide is a BCRP inhibitor. Avoid coadministration with BCRP inhibitors. If use is unavoidable, closely monitor for adverse reactions and consider dose reduction of BCRP substrate drug (refer BCRP substrate prescribing information).

  • darunavir

    cimetidine will increase the level or effect of darunavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • dasatinib

    cimetidine will increase the level or effect of dasatinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.cimetidine will decrease the level or effect of dasatinib by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • dexamethasone

    cimetidine will increase the level or effect of dexamethasone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • diazepam

    cimetidine will increase the level or effect of diazepam by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • difenoxin hcl

    cimetidine increases effects of difenoxin hcl by decreasing metabolism. Avoid or Use Alternate Drug.

  • dihydroergotamine

    cimetidine will increase the level or effect of dihydroergotamine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • dihydroergotamine intranasal

    cimetidine will increase the level or effect of dihydroergotamine intranasal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • diphenoxylate hcl

    cimetidine increases effects of diphenoxylate hcl by decreasing metabolism. Avoid or Use Alternate Drug.

  • dofetilide

    cimetidine will increase the level or effect of dofetilide by basic (cationic) drug competition for renal tubular clearance. Avoid or Use Alternate Drug.

  • dronedarone

    cimetidine will increase the level or effect of dronedarone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • duloxetine

    cimetidine will increase the level or effect of duloxetine by affecting hepatic enzyme CYP1A2 metabolism. Avoid or Use Alternate Drug.

  • eletriptan

    cimetidine will increase the level or effect of eletriptan by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • eliglustat

    cimetidine increases levels of eliglustat by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. Moderate CYP3A4 inhibitors are not recommended with eliglustat poor or intermediate metabolizers; reduce eliglustat dose from 84 mg BID to 84 mg once daily in extensive metabolizers .

  • enasidenib

    enasidenib will increase the level or effect of cimetidine by Other (see comment). Avoid or Use Alternate Drug. Avoid coadministration of enasidenib with sensitive OATP1B1, OATP1B3, or BCRP substrates, for which minimal concentration changes may lead to serious toxicities. If unavoidable, decrease the substrate(s) dosage in accordance with their Prescribing Information.

  • erdafitinib

    erdafitinib will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Avoid or Use Alternate Drug. If coadministration unavoidable, separate administration by at least 6 hr before or after administration of P-gp substrates with narrow therapeutic index.

  • ergotamine

    cimetidine will increase the level or effect of ergotamine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • erythromycin base

    cimetidine will increase the level or effect of erythromycin base by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • erythromycin ethylsuccinate

    cimetidine will increase the level or effect of erythromycin ethylsuccinate by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • erythromycin lactobionate

    cimetidine will increase the level or effect of erythromycin lactobionate by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • erythromycin stearate

    cimetidine will increase the level or effect of erythromycin stearate by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • estradiol

    cimetidine will increase the level or effect of estradiol by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • estrogens conjugated synthetic

    cimetidine will increase the level or effect of estrogens conjugated synthetic by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • estropipate

    cimetidine will increase the level or effect of estropipate by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • etravirine

    cimetidine will increase the level or effect of etravirine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • everolimus

    cimetidine will increase the level or effect of everolimus by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • fedratinib

    cimetidine will increase the level or effect of fedratinib by Other (see comment). Avoid or Use Alternate Drug. Avoid coadministration of fedratinib (a CYP3A4 and CYP2C19 substrate) with dual CYP3A4 and CYP2C19 inhibitor. Effect of coadministration of a dual CYP3A4 and CYP2C19 inhibitor with fedratinib has not been studied.

  • felodipine

    cimetidine will increase the level or effect of felodipine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • fentanyl

    cimetidine will increase the level or effect of fentanyl by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If coadministration of CYP3A4 inhibitors with fentanyl is necessary, monitor patients for respiratory depression and sedation at frequent intervals and consider fentanyl dose adjustments until stable drug effects are achieved.

  • fentanyl intranasal

    cimetidine will increase the level or effect of fentanyl intranasal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If coadministration of CYP3A4 inhibitors with fentanyl is necessary, monitor patients for respiratory depression and sedation at frequent intervals and consider fentanyl dose adjustments until stable drug effects are achieved.

  • fentanyl transdermal

    cimetidine will increase the level or effect of fentanyl transdermal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If coadministration of CYP3A4 inhibitors with fentanyl is necessary, monitor patients for respiratory depression and sedation at frequent intervals and consider fentanyl dose adjustments until stable drug effects are achieved.

  • fentanyl transmucosal

    cimetidine will increase the level or effect of fentanyl transmucosal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If coadministration of CYP3A4 inhibitors with fentanyl is necessary, monitor patients for respiratory depression and sedation at frequent intervals and consider fentanyl dose adjustments until stable drug effects are achieved.

  • fesoterodine

    cimetidine will increase the level or effect of fesoterodine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • fludrocortisone

    cimetidine will increase the level or effect of fludrocortisone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • fluoxetine

    fluoxetine will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Avoid or Use Alternate Drug.

  • fluvoxamine

    fluvoxamine will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Avoid or Use Alternate Drug.

  • fosamprenavir

    cimetidine will increase the level or effect of fosamprenavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • fosaprepitant

    cimetidine will increase the level or effect of fosaprepitant by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • hydrocortisone

    cimetidine will increase the level or effect of hydrocortisone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • hydromorphone

    cimetidine increases effects of hydromorphone by decreasing metabolism. Avoid or Use Alternate Drug.

  • hydroxyprogesterone caproate (DSC)

    cimetidine will increase the level or effect of hydroxyprogesterone caproate (DSC) by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • iloperidone

    cimetidine will increase the level or effect of iloperidone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • infigratinib (DSC)

    cimetidine will decrease the level or effect of infigratinib (DSC) by inhibition of GI absorption. Applies only to oral form of both agents. Avoid or Use Alternate Drug. If use with an acid-reducing agent cannot be avoided, administer infigratinib 2 hr before or 10 hr after administration of a H2-antagonist.

  • irinotecan

    cimetidine will increase the level or effect of irinotecan by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • irinotecan liposomal

    cimetidine will increase the level or effect of irinotecan liposomal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • ivabradine

    cimetidine will increase the level or effect of ivabradine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. Avoid coadministration of ivabradine with moderate CYP3A4 inhibitors.

  • ivacaftor

    ivacaftor increases levels of cimetidine by P-glycoprotein (MDR1) efflux transporter. Avoid or Use Alternate Drug. Ivacaftor and its M1 metabolite has the potential to inhibit P-gp; may significantly increase systemic exposure to sensitive P-gp substrates with a narrow therapeutic index.

  • ixabepilone

    cimetidine will increase the level or effect of ixabepilone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • ketoconazole

    cimetidine will decrease the level or effect of ketoconazole by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • lasmiditan

    lasmiditan increases levels of cimetidine by Other (see comment). Avoid or Use Alternate Drug.
    Comment: Lasmiditan inhibits BCRP in vitro. Avoid coadministration of lasmiditan with BCRP substrates.

  • leniolisib

    leniolisib will increase the level or effect of cimetidine by Other (see comment). Avoid or Use Alternate Drug. Leniolisib, a BCRP inhibitor, may increase systemic exposure of BCRP substrates

  • levoketoconazole

    cimetidine will decrease the level or effect of levoketoconazole by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • levorphanol

    cimetidine increases effects of levorphanol by decreasing metabolism. Avoid or Use Alternate Drug.

  • lonafarnib

    cimetidine will increase the level or effect of lonafarnib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If coadministration of lonafarnib (a sensitive CYP3A substrate) with weak CYP3A inhibitors is unavoidable, reduce to, or continue lonafarnib at starting dose. Closely monitor for arrhythmias and events (eg, syncope, heart palpitations) since lonafarnib effect on QT interval is unknown.

  • lopinavir

    cimetidine will increase the level or effect of lopinavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • loratadine

    cimetidine will increase the level or effect of loratadine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • lovastatin

    cimetidine will increase the level or effect of lovastatin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • lumefantrine

    cimetidine will increase the level or effect of lumefantrine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • maraviroc

    cimetidine will increase the level or effect of maraviroc by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • meperidine

    cimetidine increases effects of meperidine by decreasing metabolism. Avoid or Use Alternate Drug.

  • mestranol

    cimetidine will increase the level or effect of mestranol by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • methadone

    cimetidine will increase the level or effect of methadone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.cimetidine increases effects of methadone by decreasing metabolism. Avoid or Use Alternate Drug.

  • midazolam

    cimetidine will increase the level or effect of midazolam by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • morphine

    cimetidine increases effects of morphine by decreasing metabolism. Avoid or Use Alternate Drug.

  • nalbuphine

    cimetidine increases effects of nalbuphine by decreasing metabolism. Avoid or Use Alternate Drug.

  • nelfinavir

    cimetidine will increase the level or effect of nelfinavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • neratinib

    cimetidine will decrease the level or effect of neratinib by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • nicardipine

    cimetidine will increase the level or effect of nicardipine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • nilotinib

    cimetidine will increase the level or effect of nilotinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • nimodipine

    cimetidine will increase the level or effect of nimodipine by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • nisoldipine

    cimetidine will increase the level or effect of nisoldipine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.cimetidine will increase the level or effect of nisoldipine by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • olaparib

    cimetidine will increase the level or effect of olaparib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If coadministration with moderate CYP3A inhibitors cannot be avoided, reduce olaparib dose to 200 mg (capsule) or 150 mg (tablet) PO BID. Do not substitute tablets with capsules.

  • opium tincture

    cimetidine increases effects of opium tincture by decreasing metabolism. Avoid or Use Alternate Drug.

  • oxycodone

    cimetidine increases effects of oxycodone by decreasing metabolism. Avoid or Use Alternate Drug.

  • oxymorphone

    cimetidine increases effects of oxymorphone by decreasing metabolism. Avoid or Use Alternate Drug.

  • papaveretum

    cimetidine increases effects of papaveretum by decreasing metabolism. Avoid or Use Alternate Drug.

  • pazopanib

    cimetidine will decrease the level or effect of pazopanib by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug. Avoid coadministration of pazopanib with drugs that raise gastric pH; consider short-acting antacids in place of PPIs and H2 antagonists; separate antacid and pazopanib dosing by several hours

  • pentazocine

    cimetidine increases effects of pentazocine by decreasing metabolism. Avoid or Use Alternate Drug.

  • pexidartinib

    cimetidine will increase the level or effect of pexidartinib by inhibition of GI absorption. Applies only to oral form of both agents. Avoid or Use Alternate Drug. Separate pexidartinib by 2 hr before or 10 hr after taking an H2-antagonist.

  • pirfenidone

    cimetidine will increase the level or effect of pirfenidone by affecting hepatic enzyme CYP1A2 metabolism. Avoid or Use Alternate Drug. Avoid; coadministration of pirfenidone and moderate CYP1A2 inhibitors result in moderately increased exposure to pirfenidone; if unable to avoid, decrease dose of moderate CYP1A2 inhibitor

  • ponatinib

    cimetidine decreases levels of ponatinib by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug.

  • prednisone

    cimetidine will increase the level or effect of prednisone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • procainamide

    cimetidine will increase the level or effect of procainamide by basic (cationic) drug competition for renal tubular clearance. Avoid or Use Alternate Drug.

  • quetiapine

    cimetidine will increase the level or effect of quetiapine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • quinidine

    cimetidine will increase the level or effect of quinidine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.quinidine will increase the level or effect of cimetidine by basic (cationic) drug competition for renal tubular clearance. Avoid or Use Alternate Drug.

  • ranolazine

    cimetidine will increase the level or effect of ranolazine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • repaglinide

    cimetidine will increase the level or effect of repaglinide by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • risedronate

    cimetidine will increase the level or effect of risedronate by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug. Applies only to delayed release formulation; accelerates pH-sensitive dissolution of delayed release risedronate

  • ritonavir

    cimetidine will increase the level or effect of ritonavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • romidepsin

    cimetidine will increase the level or effect of romidepsin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • secretin

    cimetidine, secretin. Other (see comment). Avoid or Use Alternate Drug.
    Comment: Concomitant use of H2-receptor antagonists may cause a hyperresponse in gastrin secretion in response to stimulation testing with secretin, falsely suggesting gastrinoma. Discontinue H2-receptor antagonists at least 2 days before administering secretin to aid in the diagnosis of gastrinoma.

  • silodosin

    cimetidine will increase the level or effect of silodosin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • simvastatin

    cimetidine will increase the level or effect of simvastatin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • sirolimus

    cimetidine will increase the level or effect of sirolimus by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • solifenacin

    cimetidine will increase the level or effect of solifenacin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • sotorasib

    cimetidine will decrease the level or effect of sotorasib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If use with an acid-reducing agent cannot be avoided, administer sotorasib 4 hr before or 10 hr after administration of a locally-acting antacid.sotorasib will decrease the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Avoid or Use Alternate Drug. If use is unavoidable, refer to the prescribing information of the P-gp substrate for dosage modifications.

  • sparsentan

    cimetidine decreases effects of sparsentan by increasing gastric pH. Applies only to oral form of both agents. Avoid or Use Alternate Drug. H2-antagonists may decrease sparsentan exposure which may reduce efficacy of sparsentan.

  • sufentanil

    cimetidine increases effects of sufentanil by decreasing metabolism. Avoid or Use Alternate Drug.

  • sunitinib

    cimetidine will increase the level or effect of sunitinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • tacrolimus

    cimetidine will increase the level or effect of tacrolimus by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • tafenoquine

    tafenoquine will increase the level or effect of cimetidine by Other (see comment). Avoid or Use Alternate Drug. Tafenoquine inhibits organic cation transporter-2 (OCT2) and multidrug and toxin extrusion (MATE) transporters in vitro. Avoid coadministration with OCT2 or MATE substrates. If coadministration cannot be avoided, monitor for substrate-related toxicities and consider dosage reduction if needed based on product labeling of the coadministered drug.

  • tapentadol

    cimetidine increases effects of tapentadol by decreasing metabolism. Avoid or Use Alternate Drug.

  • temsirolimus

    cimetidine will increase the level or effect of temsirolimus by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • tepotinib

    tepotinib will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Avoid or Use Alternate Drug. If concomitant use unavoidable, reduce the P-gp substrate dosage if recommended in its approved product labeling.

  • theophylline

    cimetidine will increase the level or effect of theophylline by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • thioridazine

    cimetidine will increase the level or effect of thioridazine by affecting hepatic enzyme CYP2D6 metabolism. Avoid or Use Alternate Drug.

  • tipranavir

    cimetidine will increase the level or effect of tipranavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • tizanidine

    cimetidine will increase the level or effect of tizanidine by affecting hepatic enzyme CYP1A2 metabolism. Avoid or Use Alternate Drug.

  • tofacitinib

    cimetidine increases levels of tofacitinib by decreasing metabolism. Avoid or Use Alternate Drug. Reduce tofacitinib dose to 5 mg qDay when coadministered with 1 or more concomitant medications that result in both moderate CYP3A4 inhibition and potent CYP2C19 inhibition.

  • tolterodine

    cimetidine will increase the level or effect of tolterodine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • tolvaptan

    cimetidine will increase the level or effect of tolvaptan by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • triamcinolone acetonide injectable suspension

    cimetidine will increase the level or effect of triamcinolone acetonide injectable suspension by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • triazolam

    cimetidine will increase the level or effect of triazolam by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • trilaciclib

    trilaciclib will decrease the level or effect of cimetidine by Other (see comment). Avoid or Use Alternate Drug. Avoid coadministration of trilaciclib (OCT2, MATE1, and MATE-2K inhibitor) with substrates where minimal increased concentration in kidney or blood may lead to serious or life-threatening toxicities.

  • verapamil

    cimetidine will increase the level or effect of verapamil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug.

  • vilazodone

    cimetidine increases levels of vilazodone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Avoid or Use Alternate Drug. If intolerable adverse effects occur when coadministered with moderate CYP3A4 inhibitors, reduce daily dose to 20 mg.

  • warfarin

    cimetidine increases effects of warfarin by unspecified interaction mechanism. Avoid or Use Alternate Drug.

  • acalabrutinib

    cimetidine decreases levels of acalabrutinib by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Acalabrutinib solubility decreases with increasing gastric pH. Administer acalabrutinib 2 hr before an H2-receptor antagonist.acalabrutinib increases levels of cimetidine by Other (see comment). Use Caution/Monitor.
    Comment: Acalabrutinib may increase exposure to coadministered BCRP substrates by inhibition of intestinal BCRP.

  • alfentanil

    cimetidine will increase the level or effect of alfentanil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • alfuzosin

    cimetidine will increase the level or effect of alfuzosin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • alosetron

    cimetidine will increase the level or effect of alosetron by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • amitriptyline

    cimetidine will increase the level or effect of amitriptyline by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • apalutamide

    apalutamide will decrease the level or effect of cimetidine by increasing elimination. Use Caution/Monitor. Apalutamide weakly induces BCRP and may decrease systemic exposure of drugs that are BCRP substrates.

  • armodafinil

    cimetidine will increase the level or effect of armodafinil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • atazanavir

    cimetidine will increase the level or effect of atazanavir by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • atogepant

    cimetidine will increase the level or effect of atogepant by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • atomoxetine

    cimetidine will increase the level or effect of atomoxetine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • avanafil

    cimetidine will increase the level or effect of avanafil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. CYP3A4 inhibitors may reduce avanafil clearance increasing systemic exposure to avanafil; increased levels may result in increased associated adverse events; the maximum recommended dose of STENDRA is 50 mg, not to exceed once every 24 hours for patients taking concomitant moderate CYP3A4 inhibitors

  • avapritinib

    cimetidine will increase the level or effect of avapritinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • azelastine

    cimetidine increases effects of azelastine by decreasing metabolism. Use Caution/Monitor.

  • bendamustine

    cimetidine increases levels of bendamustine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor. Consider alternate therapy due to risk of increased bendamustine exposure and adverse effects. In vitro, bendamustine is a CYP1A2 substrate.

  • benzhydrocodone/acetaminophen

    cimetidine will increase the level or effect of benzhydrocodone/acetaminophen by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor. Hydromorphone (<3% of the circulating parent hydrocodone [benzhydrocodone is prodrug of hydrocodone]) is mainly formed by CYP2D6 mediated O-demethylation of hydrocodone. Hydromorphone may contribute to the total analgesic effect of hydrocodone.

  • berotralstat

    berotralstat will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Monitor or titrate P-gp substrate dose if coadministered.

  • bexarotene

    cimetidine will increase the level or effect of bexarotene by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • bortezomib

    cimetidine will increase the level or effect of bortezomib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • bosentan

    cimetidine will increase the level or effect of bosentan by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • bosutinib

    bosutinib increases levels of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor.

  • brexpiprazole

    cimetidine will increase the level or effect of brexpiprazole by affecting hepatic enzyme CYP2D6 metabolism. Modify Therapy/Monitor Closely. Administer a quarter of brexpiprazole dose if coadministered with a moderate CYP2D6 inhibitor PLUS a strong/moderate CYP3A4 inhibitor. cimetidine will increase the level or effect of brexpiprazole by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Administer a quarter of brexpiprazole dose if coadministered with a moderate CYP3A4 inhibitor PLUS a strong/moderate CYP2D6 inhibitor.

  • budesonide

    cimetidine decreases effects of budesonide by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Enteric-coated budesonide dissolves at pH >5.5. Also, dissolution of extended-release budesonide tablets is pH dependent. Coadministration with drugs that increase gastric pH may cause these budesonide products to prematurely dissolve, and possibly affect release properties and absorption of the drug in the duodenum.

  • cabazitaxel

    cimetidine will increase the level or effect of cabazitaxel by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. Caution should be exercised with concomitant use of moderate CYP3A4 inhibitors.

  • cabozantinib

    cimetidine will increase the level or effect of cabozantinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • carbamazepine

    cimetidine will increase the level or effect of carbamazepine by decreasing metabolism. Modify Therapy/Monitor Closely. Monitor plasma levels when used concomitantly

  • carbonyl iron

    cimetidine will decrease the level or effect of carbonyl iron by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • carmustine

    cimetidine, carmustine. Mechanism: decreasing metabolism. Use Caution/Monitor. Enhanced myelotoxicity.

  • carvedilol

    cimetidine will increase the level or effect of carvedilol by affecting hepatic enzyme CYP2C9/10 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of carvedilol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • cefdinir

    cimetidine will decrease the level or effect of cefdinir by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • cefditoren

    cimetidine will decrease the level or effect of cefditoren by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • cefpodoxime

    cimetidine will decrease the level or effect of cefpodoxime by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • cefuroxime

    cimetidine will decrease the level or effect of cefuroxime by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • cevimeline

    cimetidine will increase the level or effect of cevimeline by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • chlordiazepoxide

    cimetidine increases levels of chlordiazepoxide by decreasing metabolism. Use Caution/Monitor.

  • cilostazol

    cimetidine increases toxicity of cilostazol by affecting hepatic enzyme CYP2C19 metabolism. Modify Therapy/Monitor Closely. Consider decreasing cilostazol dose; moderate CYP2C19 inhibitors may increase serum levels of 3,4-dehydrocilostazol (active metabolite).

  • citalopram

    cimetidine increases levels of citalopram by affecting hepatic enzyme CYP2C19 metabolism. Use Caution/Monitor. Citalopram 20 mg/day is the maximum recommended dose for patients taking CYP2C19 inhibitors because of the risk of QT prolongation.

  • clarithromycin

    cimetidine will increase the level or effect of clarithromycin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.clarithromycin will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor.

  • clomipramine

    cimetidine will increase the level or effect of clomipramine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of clomipramine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of clomipramine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • clonazepam

    cimetidine increases levels of clonazepam by decreasing metabolism. Use Caution/Monitor.

  • clopidogrel

    cimetidine decreases effects of clopidogrel by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. Clopidogrel efficacy may be reduced by drugs that inhibit CYP3A4. Inhibition of platelet aggregation by clopidogrel is entirely due to an active metabolite. Clopidogrel is metabolized to this active metabolite in part by CYP3A4. .

  • clorazepate

    cimetidine increases levels of clorazepate by decreasing metabolism. Use Caution/Monitor.

  • clozapine

    cimetidine will increase the level or effect of clozapine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.

  • codeine

    cimetidine will increase the level or effect of codeine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor. Prevents conversion of codeine to its active metabolite morphine.

  • conivaptan

    cimetidine will increase the level or effect of conivaptan by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • crizotinib

    cimetidine decreases levels of crizotinib by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor. Drugs that elevate the gastric pH may decrease the solubility of crizotinib and subsequently reduce its bioavailability. However, no formal studies have been conducted. .

  • dabrafenib

    cimetidine will decrease the level or effect of dabrafenib by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor. Drugs that alter upper GI tract pH (eg, PPIs, H2-blockers, antacids) may decrease dabrafenib solubility and reduce its bioavailability

  • danicopan

    danicopan will increase the level or effect of cimetidine by Other (see comment). Use Caution/Monitor. Danicopan increases plasma concentrations of BCRP substrates; consider dose reduction of BCRP substrate according to its prescribing information.danicopan will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Danicopan increases plasma concentrations of P-gp substrates; consider dose reduction of P-gp substrates where minimal concentration changes may lead to serious adverse reactions.

  • desipramine

    cimetidine will increase the level or effect of desipramine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • dexmethylphenidate

    cimetidine will increase the level or effect of dexmethylphenidate by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Applies only to extended release formulation

  • dienogest/estradiol valerate

    cimetidine will increase the level or effect of dienogest/estradiol valerate by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. Monitor for potential adverse effects such as nausea, irregular uterine bleeding, breast tenderness and headache.

  • diltiazem

    cimetidine will increase the level or effect of diltiazem by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Consider alternatives to cimetidine in patients receiving diltiazem. If no alternative is available, monitor for the effects of diltiazem following cimetidine initiation/discontinuation.cimetidine will increase the level or effect of diltiazem by basic (cationic) drug competition for renal tubular clearance. Modify Therapy/Monitor Closely. Exercise caution when concomitantly using diltiazem with atazanavir. Consider reducing the diltiazem dose by 50%. ECG monitoring is recommended.

  • disopyramide

    cimetidine will increase the level or effect of disopyramide by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • docetaxel

    cimetidine will increase the level or effect of docetaxel by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • donepezil

    cimetidine will increase the level or effect of donepezil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • doxepin

    cimetidine will increase the level or effect of doxepin by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • doxepin cream

    cimetidine increases levels of doxepin cream by decreasing metabolism. Use Caution/Monitor.

  • doxorubicin

    cimetidine will increase the level or effect of doxorubicin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • doxorubicin liposomal

    cimetidine will increase the level or effect of doxorubicin liposomal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • duloxetine

    cimetidine will increase the level or effect of duloxetine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • dutasteride

    cimetidine will increase the level or effect of dutasteride by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • elagolix

    elagolix will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor.

  • eliglustat

    eliglustat increases levels of cimetidine by P-glycoprotein (MDR1) efflux transporter. Modify Therapy/Monitor Closely. Monitor therapeutic drug concentrations, as indicated, or consider reducing the dosage of the P-gp substrate and titrate to clinical effect.

  • eluxadoline

    cimetidine increases levels of eluxadoline by affecting hepatic enzyme CYP2C19 metabolism. Use Caution/Monitor. As a precautionary measure due to incomplete information on the metabolism of eluxadoline, use caution when coadministered with strong CYP2C19 inhibitors.eluxadoline increases levels of cimetidine by decreasing metabolism. Use Caution/Monitor. Eluxadoline may increase the systemic exposure of coadministered BCRP substrates.

  • encorafenib

    encorafenib will increase the level or effect of cimetidine by Other (see comment). Modify Therapy/Monitor Closely. Encorafenib (a BCRP inhibitor) may increase the concentration and toxicities of BCRP substrates. Closely monitor for signs and symptoms of increased exposure and consider adjusting the dose of these substrates.

  • epirubicin

    cimetidine increases levels of epirubicin by decreasing metabolism. Use Caution/Monitor. Cimetidine increased the AUC of epirubicin by 50%. Cimetidine treatment should be stopped during treatment with epirubicin.

  • eplerenone

    cimetidine will increase the level or effect of eplerenone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • erdafitinib

    erdafitinib increases levels of cimetidine by decreasing renal clearance. Modify Therapy/Monitor Closely. Consider alternatives that are not OCT2 substrates or consider reducing the dose of OCT2 substrates based on tolerability.

  • erlotinib

    cimetidine decreases levels of erlotinib by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Separate administration by taking erlotinib 2 hr before or 10 hr after H2 blockers. Coadministration of H2-blockers and erlotinib may decrease erlotinib exposure and reduce its efficacy.

  • eslicarbazepine acetate

    eslicarbazepine acetate will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Use Caution/Monitor.

  • estrogens esterified

    cimetidine will increase the level or effect of estrogens esterified by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • ethinylestradiol

    cimetidine will increase the level or effect of ethinylestradiol by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • etoposide

    cimetidine will increase the level or effect of etoposide by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • etravirine

    cimetidine will increase the level or effect of etravirine by affecting hepatic enzyme CYP2C9/10 metabolism. Use Caution/Monitor.

  • eucalyptus

    cimetidine will increase the level or effect of eucalyptus by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • ferric maltol

    cimetidine will decrease the level or effect of ferric maltol by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • ferrous fumarate

    cimetidine will decrease the level or effect of ferrous fumarate by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • ferrous gluconate

    cimetidine will decrease the level or effect of ferrous gluconate by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • ferrous sulfate

    cimetidine will decrease the level or effect of ferrous sulfate by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • finerenone

    cimetidine will increase the level or effect of finerenone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Monitor serum potassium during initiation and dosage adjustment of either finererone or weak CYP3A4 inhibitors. Adjust finererone dosage as needed.

  • flecainide

    cimetidine will increase the level or effect of flecainide by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor. Flecainide dosage should be carefully titrated on initiation of therapy. Careful monitoring of flecainide plasma concentration should be instituted when cimetidine is coadministered or discontinued.

  • flibanserin

    cimetidine will increase the level or effect of flibanserin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. Increased flibanserin adverse effects may occur if coadministered with multiple weak CYP3A4 inhibitors.

  • fluoxetine

    cimetidine will increase the level or effect of fluoxetine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • fluvastatin

    cimetidine increases levels of fluvastatin by decreasing metabolism. Use Caution/Monitor.

  • fluvoxamine

    cimetidine will increase the level or effect of fluvoxamine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • fosamprenavir

    cimetidine will decrease the level or effect of fosamprenavir by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • fosphenytoin

    cimetidine will increase the level or effect of fosphenytoin by affecting hepatic enzyme CYP2C9/10 metabolism. Use Caution/Monitor.

  • fostamatinib

    fostamatinib will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Concomitant use of fostamatinib may increase concentrations of P-gp substrates. Monitor for toxicities of the P-gp substrate drug that may require dosage reduction when given concurrently with fostamatinib.

  • fostemsavir

    fostemsavir will increase the level or effect of cimetidine by Other (see comment). Modify Therapy/Monitor Closely. Fostemsavir inhibits BCRP transporters. If possible, avoid coadministration or modify dose of BCRP substrate coadministered with fostemsavir.

  • gefitinib

    cimetidine decreases levels of gefitinib by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor. Separate gefitinib and H2-antagonist doses by at least 6 hr.

  • glecaprevir/pibrentasvir

    glecaprevir/pibrentasvir will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor.

  • glipizide

    cimetidine will increase the level or effect of glipizide by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • glyburide

    cimetidine will increase the level or effect of glyburide by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • haloperidol

    cimetidine will increase the level or effect of haloperidol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • hydrocodone

    cimetidine will increase the level or effect of hydrocodone by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor. Hydromorphone (<3% of the circulating parent hydrocodone) is mainly formed by CYP2D6 mediated O-demethylation of hydrocodone. Hydromorphone may contribute to the total analgesic effect of hydrocodone.

  • hydromorphone

    cimetidine will increase the level or effect of hydromorphone by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • iloperidone

    cimetidine will increase the level or effect of iloperidone by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • imatinib

    cimetidine will increase the level or effect of imatinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • imipramine

    cimetidine will increase the level or effect of imipramine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of imipramine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of imipramine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • iron dextran complex

    cimetidine will decrease the level or effect of iron dextran complex by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • iron sucrose

    cimetidine will decrease the level or effect of iron sucrose by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • isavuconazonium sulfate

    cimetidine will increase the level or effect of isavuconazonium sulfate by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • isoniazid

    isoniazid will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Use Caution/Monitor.

  • isradipine

    cimetidine will increase the level or effect of isradipine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • istradefylline

    istradefylline will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Istradefylline 40 mg/day increased peak levels and AUC of P-gp substrates in clinical trials. Consider dose reduction of sensitive P-gp substrates.

  • itraconazole

    cimetidine will decrease the level or effect of itraconazole by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Administer acid neutralizing medicines at least 2 hours before or 2 hours after itraconazole. When taking with cimetidine, administer with non-diet cola to increase GI acidity.

  • ivacaftor

    cimetidine increases levels of ivacaftor by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. Reduce ivacaftor dose if coadministered with moderate CYP3A4 inhibitors. See specific ivacaftor-containing product for precise dosage modification. .

  • ketoconazole

    cimetidine will increase the level or effect of ketoconazole by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • lapatinib

    cimetidine will decrease the level or effect of lapatinib by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • ledipasvir/sofosbuvir

    cimetidine decreases levels of ledipasvir/sofosbuvir by Other (see comment). Use Caution/Monitor.
    Comment: Ledipasvir solubility decreases as pH increases; drugs that increase gastric pH are expected to decrease levels of ledipasvir; H2-receptor antagonists may be administered simultaneously with or 12 hr apart from ledipasvir/sofosbuvir at a dose that does not exceed doses comparable to famotidine 40 mg BID.

  • lemborexant

    cimetidine will increase the level or effect of lemborexant by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Lower nightly dose of lemborexant recommended if coadministered with weak CYP3A4 inhibitors. See drug monograph for specific dosage modification.

  • levoketoconazole

    cimetidine will increase the level or effect of levoketoconazole by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • lidocaine

    cimetidine will increase the level or effect of lidocaine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.

  • lomitapide

    lomitapide increases levels of cimetidine by P-glycoprotein (MDR1) efflux transporter. Modify Therapy/Monitor Closely. Consider reducing dose when used concomitantly with lomitapide.

  • lomustine

    cimetidine, lomustine. Mechanism: decreasing metabolism. Use Caution/Monitor. Enhanced myelotoxicity.

  • lonafarnib

    lonafarnib will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Modify Therapy/Monitor Closely. Lonafarnib is a weak P-gp inhibitor. Monitor for adverse reactions if coadministered with P-gp substrates where minimal concentration changes may lead to serious or life-threatening toxicities. Reduce P-gp substrate dose if needed.

  • lurasidone

    cimetidine increases levels of lurasidone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Manufacturer recommends decreasing starting dose of lurasidone to 20 mg/day and maximum daily dose of lurasidone 80 mg when coadministered with moderate CYP3A4 inhibitors. Concurrent use may increase risk of lurasidone-related adverse reactions.

  • mavacamten

    cimetidine increases levels of mavacamten by affecting hepatic enzyme CYP2C19 metabolism. Modify Therapy/Monitor Closely. Modify mavacamten dose if coadministered with weak or moderate CYP2C19 inhibitors.

  • mavorixafor

    mavorixafor will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Caution if mavorixafor (a P-gp inhibitor) is coadministered with a sensitive P-gp substrate where minimal substrate concentration changes may lead to serious adverse effects.

  • mebendazole

    cimetidine increases levels of mebendazole by decreasing metabolism. Use Caution/Monitor.

  • mefloquine

    cimetidine will increase the level or effect of mefloquine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • melatonin

    cimetidine will increase the level or effect of melatonin by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor. Monitor melatonin effects if coadministered with moderate CYP1A2 inhibitors

  • memantine

    cimetidine will increase the level or effect of memantine by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • metformin

    cimetidine will increase the level or effect of metformin by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • methamphetamine

    cimetidine will increase the level or effect of methamphetamine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • methylphenidate

    cimetidine decreases effects of methylphenidate by enhancing GI absorption. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Since the characteristics of methylphenidate extended release capsules (Ritalin LA) are pH dependent, coadministration of antacids or acid suppressants could alter the release of methylphenidate. Consider separating the administration of the antacid and the methylphenidate extended-release capsules may be avoided.

  • metoprolol

    cimetidine will increase the level or effect of metoprolol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • mexiletine

    cimetidine will increase the level or effect of mexiletine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of mexiletine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • midazolam intranasal

    cimetidine will increase the level or effect of midazolam intranasal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. Coadministration of mild CYP3A4 inhibitors with midazolam intranasal may cause higher midazolam systemic exposure, which may prolong sedation.

  • midodrine

    cimetidine will increase the level or effect of midodrine by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • mizolastine

    cimetidine increases levels of mizolastine by decreasing metabolism. Use Caution/Monitor.

  • momelotinib

    momelotinib increases toxicity of cimetidine by plasma protein binding competition. Modify Therapy/Monitor Closely. Momelotinib (BCRP inhibitor) may increase exposure of BCRP substrates, which may increase the risk of BCRP substrate adverse reactions. Dose adjustment of other BCRP substrates may necessary.

  • morphine

    cimetidine will increase the level or effect of morphine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • nateglinide

    cimetidine will increase the level or effect of nateglinide by affecting hepatic enzyme CYP2C9/10 metabolism. Use Caution/Monitor.

  • nebivolol

    cimetidine will increase the level or effect of nebivolol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • nelfinavir

    cimetidine will increase the level or effect of nelfinavir by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • nicotine inhaled

    cimetidine increases levels of nicotine inhaled by decreasing renal clearance. Use Caution/Monitor.

  • nicotine intranasal

    cimetidine increases levels of nicotine intranasal by decreasing metabolism. Use Caution/Monitor.cimetidine increases levels of nicotine intranasal by decreasing renal clearance. Use Caution/Monitor.

  • nifedipine

    cimetidine will increase the level or effect of nifedipine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • nilotinib

    cimetidine decreases levels of nilotinib by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Avoid this interaction by administering H2 antagonists 10 hr after or 2 hr before nilotinib.

  • nimodipine

    cimetidine will increase the level or effect of nimodipine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • nortriptyline

    cimetidine will increase the level or effect of nortriptyline by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • olanzapine

    cimetidine will increase the level or effect of olanzapine by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.

  • oliceridine

    cimetidine will increase the level or effect of oliceridine by affecting hepatic enzyme CYP2D6 metabolism. Modify Therapy/Monitor Closely. If concomitant use is necessary, may require less frequent oliceridine dosing. Closely monitor for respiratory depression and sedation and titrate subsequent doses accordingly. If inhibitor is discontinued, consider increase oliceridine dosage until stable drug effects are achieved. Monitor for signs of opioid withdrawal.

  • oteseconazole

    oteseconazole will increase the level or effect of cimetidine by Other (see comment). Modify Therapy/Monitor Closely. Otesezonale, a BCRP inhibitor, may increase the effects and risk of toxicities of BCRP substrates. Use lowest starting dose of BCRP substrate, or consider reducing BCRP substrate dose.

  • oxybutynin

    cimetidine will increase the level or effect of oxybutynin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • oxycodone

    cimetidine will increase the level or effect of oxycodone by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • oxymorphone

    cimetidine will increase the level or effect of oxymorphone by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • paclitaxel

    cimetidine will increase the level or effect of paclitaxel by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • paclitaxel protein bound

    cimetidine will increase the level or effect of paclitaxel protein bound by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • palbociclib

    cimetidine will increase the level or effect of palbociclib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • parecoxib

    cimetidine will increase the level or effect of parecoxib by affecting hepatic enzyme CYP2C9/10 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of parecoxib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • paroxetine

    cimetidine will increase the level or effect of paroxetine by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • pentoxifylline

    cimetidine will increase the level or effect of pentoxifylline by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.

  • phenytoin

    cimetidine will increase the level or effect of phenytoin by affecting hepatic enzyme CYP2C9/10 metabolism. Use Caution/Monitor.

  • pimozide

    cimetidine will increase the level or effect of pimozide by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • pioglitazone

    cimetidine will increase the level or effect of pioglitazone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • polysaccharide iron

    cimetidine will decrease the level or effect of polysaccharide iron by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • ponatinib

    ponatinib increases levels of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor.ponatinib increases levels of cimetidine by Other (see comment). Use Caution/Monitor.

  • posaconazole

    cimetidine will decrease the level or effect of posaconazole by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • pramipexole

    cimetidine will increase the level or effect of pramipexole by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • praziquantel

    cimetidine increases levels of praziquantel by decreasing metabolism. Use Caution/Monitor.

  • propafenone

    cimetidine will increase the level or effect of propafenone by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of propafenone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • propranolol

    cimetidine will increase the level or effect of propranolol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • quinine

    cimetidine will increase the level or effect of quinine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of quinine by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • rabeprazole

    cimetidine will increase the level or effect of rabeprazole by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • ramelteon

    cimetidine will increase the level or effect of ramelteon by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.cimetidine will increase the level or effect of ramelteon by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • rasagiline

    cimetidine will increase the level or effect of rasagiline by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor. Recommended dose of rasagiline is 0.5mg daily in combination with CYP1A2 inhibitors.

  • regorafenib

    regorafenib will increase the level or effect of cimetidine by Other (see comment). Modify Therapy/Monitor Closely. Regorafenib likely inhibits BCRP (ABCG2) transport. Coadministration with a BCRP substrate may increase systemic exposure to the substrate and related toxicity.

  • rilpivirine

    cimetidine will decrease the level or effect of rilpivirine by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Concurrent use, may cause treatment failure and/or the development of rilpivirine or NNRTI resistance owing to decreased levels. Administer H2 antagonists at least 12 hours before or at least 4 hours after rilpivirine.

  • roflumilast

    cimetidine increases levels of roflumilast by Other (see comment). Modify Therapy/Monitor Closely.
    Comment: Coadministration with dual inhibitors of CYP3A4 and CYP1A2 may increase systemic exposure and result in increased adverse reactions.

  • roflumilast topical

    cimetidine will increase the level or effect of roflumilast topical by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • ropinirole

    cimetidine will increase the level or effect of ropinirole by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.

  • rose hips

    cimetidine will decrease the level or effect of rose hips by increasing gastric pH. Applies only to oral form of both agents. Use Caution/Monitor.

  • ruxolitinib

    cimetidine will increase the level or effect of ruxolitinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • ruxolitinib topical

    cimetidine will increase the level or effect of ruxolitinib topical by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • safinamide

    safinamide will increase the level or effect of cimetidine by Other (see comment). Use Caution/Monitor. Safinamide and its major metabolite may inhibit intestinal BCRP. Monitor BCRP substrates for increased pharmacologic or adverse effects.

  • sarecycline

    sarecycline will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Monitor for toxicities of P-gp substrates that may require dosage reduction when coadministered with P-gp inhibitors.

  • saxagliptin

    cimetidine will increase the level or effect of saxagliptin by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • serdexmethylphenidate/dexmethylphenidate

    cimetidine will increase the level or effect of serdexmethylphenidate/dexmethylphenidate by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Applies only to extended release formulation

  • sildenafil

    cimetidine will increase the level or effect of sildenafil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • sofosbuvir/velpatasvir

    cimetidine will decrease the level or effect of sofosbuvir/velpatasvir by increasing gastric pH. Applies only to oral form of both agents. Modify Therapy/Monitor Closely. Velpatasvir solubility decreases as gastric pH increases (practically insoluble at pH >5). H2 receptor antagonists may be administered simultaneously with or 12 hr apart from sofosbuvir/velpatasvir at a dose that does not exceed doses comparable to famotidine 40 mg BID.sofosbuvir/velpatasvir will increase the level or effect of cimetidine by Other (see comment). Use Caution/Monitor. Velpatasvir is an inhibitor of the drug transporter BCRP. Coadministration may increase systemic exposure of drugs that are BCRP substrates.

  • sonidegib

    cimetidine will increase the level or effect of sonidegib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Avoid coadministration of sonidegib with moderate CYP3A4 inhibitors. If a moderate CYP3A inhibitor must be used, administer the moderate CYP3A inhibitor for <14 days and monitor closely for adverse reactions, particularly musculoskeletal adverse reactions.

  • stiripentol

    stiripentol will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Modify Therapy/Monitor Closely. Consider reducing the dose of P-glycoprotein (P-gp) substrates, if adverse reactions are experienced when administered concomitantly with stiripentol.stiripentol will increase the level or effect of cimetidine by Other (see comment). Modify Therapy/Monitor Closely. Stiripentol is a BCRP transport inhibitor. Consider dosage reduction for BCRP substrates if adverse effects are experienced when coadministered.

  • sufentanil

    cimetidine will increase the level or effect of sufentanil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • sulfamethoxazole

    cimetidine will increase the level or effect of sulfamethoxazole by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • suvorexant

    cimetidine will increase the level or effect of suvorexant by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Modify Therapy/Monitor Closely. Decrease suvorexant starting dose to 5 mg HS if coadministered with moderate CYP3A4 inhibitors

  • tadalafil

    cimetidine will increase the level or effect of tadalafil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • tafamidis

    tafamidis will increase the level or effect of cimetidine by Other (see comment). Use Caution/Monitor. Tafamidis inhibits breast cancer resistant protein (BCRP) in vitro and may increase exposure of BCRP substrates following tafamidis or tafamidis meglumine administration. Dosage adjustment of these BCRP substrates may be necessary.

  • tafamidis meglumine

    tafamidis meglumine will increase the level or effect of cimetidine by Other (see comment). Use Caution/Monitor. Tafamidis inhibits breast cancer resistant protein (BCRP) in vitro and may increase exposure of BCRP substrates following tafamidis or tafamidis meglumine administration. Dosage adjustment of these BCRP substrates may be necessary.

  • tamoxifen

    cimetidine, tamoxifen. affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. CYP3A4 inhibition decreases metabolism of tamoxifen to N-desmethyl tamoxifen (active metabolite with similar biologic activity).

  • tamsulosin

    cimetidine increases levels of tamsulosin by decreasing renal clearance. Use Caution/Monitor. Decreases tamsulosin clearance by 26% resulting in increased AUC (44%).cimetidine increases levels of tamsulosin by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • tazemetostat

    cimetidine will increase the level or effect of tazemetostat by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • tenofovir DF

    cimetidine, tenofovir DF.
    Either increases levels of the other by decreasing renal clearance. Use Caution/Monitor.

  • tetanus toxoid adsorbed or fluid

    cimetidine increases levels of tetanus toxoid adsorbed or fluid by decreasing metabolism. Use Caution/Monitor.

  • theophylline

    cimetidine will increase the level or effect of theophylline by affecting hepatic enzyme CYP1A2 metabolism. Use Caution/Monitor.

  • timolol

    cimetidine will increase the level or effect of timolol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor.

  • tinidazole

    cimetidine will increase the level or effect of tinidazole by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • tofacitinib

    cimetidine increases levels of tofacitinib by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor. No specific dose adjustment recommended when tofacitinib coadministered with moderate CYP3A4 inhibitors; decrease tofacitinib dose if coadministered with both moderate CYP3A4 and potent CYP2C19 inhibitors.cimetidine increases levels of tofacitinib by affecting hepatic enzyme CYP2C19 metabolism. Use Caution/Monitor. No specific dose adjustment recommended when tofacitinib coadministered with potent CYP2C19 inhibitors; decrease tofacitinib dose if coadministered with both moderate CYP3A4 and potent CYP2C19 inhibitors .

  • tramadol

    cimetidine decreases effects of tramadol by affecting hepatic enzyme CYP2D6 metabolism. Use Caution/Monitor. Decreased conversion of tramadol to active metabolite.cimetidine decreases effects of tramadol by decreasing metabolism. Use Caution/Monitor. Decreased conversion of tramadol to active metabolite.

  • trazodone

    cimetidine will increase the level or effect of trazodone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • triamterene

    cimetidine will increase the level or effect of triamterene by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • trimethoprim

    cimetidine will increase the level or effect of trimethoprim by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • tucatinib

    tucatinib will increase the level or effect of cimetidine by P-glycoprotein (MDR1) efflux transporter. Use Caution/Monitor. Consider reducing the dosage of P-gp substrates, where minimal concentration changes may lead to serious or life-threatening toxicities.

  • vadadustat

    vadadustat will increase the level or effect of cimetidine by Other (see comment). Use Caution/Monitor. Vadadustat may increase exposure of BCRP substrates. Monitor for signs of adverse effect of BCRP substrate and reduce substrate dose in accordance with their product labeling.

  • valacyclovir

    cimetidine increases levels of valacyclovir by decreasing renal clearance. Use Caution/Monitor.

  • vandetanib

    vandetanib increases levels of cimetidine by Other (see comment). Modify Therapy/Monitor Closely.
    Comment: Vandetanib inhibits the uptake of substrates of organic cation transporter type 2 (OCT2).

  • vardenafil

    cimetidine will increase the level or effect of vardenafil by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • verapamil

    cimetidine will increase the level or effect of verapamil by basic (cationic) drug competition for renal tubular clearance. Use Caution/Monitor.

  • vinblastine

    cimetidine will increase the level or effect of vinblastine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • vincristine

    cimetidine will increase the level or effect of vincristine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • vincristine liposomal

    cimetidine will increase the level or effect of vincristine liposomal by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • vinorelbine

    cimetidine will increase the level or effect of vinorelbine by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • xanomeline/trospium

    cimetidine, xanomeline/trospium.
    Either increases levels of the other by decreasing elimination. Use Caution/Monitor. Coadministration of trospium with other drugs eliminated by active tubular secretion may increase plasma concentrations of trospium and/or the concomitantly used drug owing to competition for this elimination pathway. Monitor for increased frequency and/or severity of adverse reactions.

  • zaleplon

    cimetidine will increase the level or effect of zaleplon by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • ziprasidone

    cimetidine will increase the level or effect of ziprasidone by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • zolmitriptan

    cimetidine increases levels of zolmitriptan by unknown mechanism. Modify Therapy/Monitor Closely. Half-life and blood levels of zolmitriptan and its active N-desmethyl metabolite are approximately doubled when coadministered with cimetidine; limit zolmitriptan to 2.5 mg/dose and 5 mg/day.

  • zolpidem

    cimetidine will increase the level or effect of zolpidem by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • zonisamide

    cimetidine will increase the level or effect of zonisamide by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Use Caution/Monitor.

  • alosetron

    cimetidine will increase the level or effect of alosetron by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • amobarbital

    amobarbital will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • amphetamine

    cimetidine will increase the level or effect of amphetamine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • antipyrine

    cimetidine will increase the level or effect of antipyrine by affecting hepatic enzyme CYP1A2 metabolism. Minor/Significance Unknown.

  • aripiprazole

    cimetidine will increase the level or effect of aripiprazole by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • armodafinil

    armodafinil will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • asenapine

    cimetidine will increase the level or effect of asenapine by affecting hepatic enzyme CYP1A2 metabolism. Minor/Significance Unknown.

  • blessed thistle

    blessed thistle decreases effects of cimetidine by pharmacodynamic antagonism. Minor/Significance Unknown. Theoretical interaction.

  • bosentan

    cimetidine will increase the level or effect of bosentan by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • butabarbital

    butabarbital will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • butalbital

    butalbital will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • caffeine

    cimetidine will increase the level or effect of caffeine by affecting hepatic enzyme CYP1A2 metabolism. Minor/Significance Unknown.

  • celecoxib

    cimetidine will increase the level or effect of celecoxib by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • chlorpromazine

    cimetidine will increase the level or effect of chlorpromazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • cyanocobalamin

    cimetidine decreases levels of cyanocobalamin by inhibition of GI absorption. Applies only to oral form of both agents. Minor/Significance Unknown.

  • devil’s claw

    devil’s claw decreases effects of cimetidine by pharmacodynamic antagonism. Minor/Significance Unknown.

  • dextroamphetamine

    cimetidine will increase the level or effect of dextroamphetamine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • dextromethorphan

    cimetidine will increase the level or effect of dextromethorphan by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • diclofenac

    cimetidine will increase the level or effect of diclofenac by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • digoxin

    cimetidine will increase the level or effect of digoxin by increasing gastric pH. Applies only to oral form of both agents. Minor/Significance Unknown.cimetidine will increase the level or effect of digoxin by basic (cationic) drug competition for renal tubular clearance. Minor/Significance Unknown.

  • donepezil

    cimetidine will increase the level or effect of donepezil by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • efavirenz

    efavirenz will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • eltrombopag

    cimetidine will increase the level or effect of eltrombopag by affecting hepatic enzyme CYP1A2 metabolism. Minor/Significance Unknown.cimetidine will increase the level or effect of eltrombopag by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • encainide

    cimetidine will increase the level or effect of encainide by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • etravirine

    etravirine will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • famciclovir

    cimetidine, famciclovir. aldehyde dehydrogenase inhibition. Minor/Significance Unknown. The conversion of 6-deoxy penciclovir to penciclovir is catalyzed by aldehyde oxidase. Interactions with other drugs metabolized by this enzyme and/or inhibiting this enzyme could potentially occur. Clinical interaction studies of famciclovir with cimetidine did not show relevant effects on the formation of penciclovir.

  • felbamate

    felbamate will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • felodipine

    felodipine will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • fesoterodine

    cimetidine will increase the level or effect of fesoterodine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • fluconazole

    fluconazole will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • fluphenazine

    cimetidine will increase the level or effect of fluphenazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • flurbiprofen

    cimetidine will increase the level or effect of flurbiprofen by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • fluvastatin

    cimetidine will increase the level or effect of fluvastatin by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • green tea

    cimetidine will increase the level or effect of green tea by affecting hepatic enzyme CYP1A2 metabolism. Minor/Significance Unknown. Green tea may contain caffeine. CYP1A2 inhibitors may inhibit the hepatic oxidative metabolism of caffeine.

  • ibuprofen

    cimetidine will increase the level or effect of ibuprofen by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • ibuprofen IV

    cimetidine will increase the level or effect of ibuprofen IV by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • isavuconazonium sulfate

    isavuconazonium sulfate will increase the level or effect of cimetidine by Other (see comment). Minor/Significance Unknown. Isavuconazonium sulfate, an OCT2 inhibitor, may increase the effects or levels of OCT2 substrates.

  • loratadine

    cimetidine will increase the level or effect of loratadine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • losartan

    cimetidine will increase the level or effect of losartan by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown. May inhibit the conversion of losartan to its active metabolite E-3174. Importance of interaction not established; monitor individual therapeutic response to determine losartan dosage.

  • modafinil

    modafinil will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • ospemifene

    cimetidine increases levels of ospemifene by affecting hepatic/intestinal enzyme CYP3A4 metabolism. Minor/Significance Unknown.

  • oxcarbazepine

    oxcarbazepine will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • parecoxib

    parecoxib will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • pefloxacin

    cimetidine increases levels of pefloxacin by decreasing metabolism. Minor/Significance Unknown.

  • pentobarbital

    pentobarbital will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • perhexiline

    cimetidine will increase the level or effect of perhexiline by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • perphenazine

    cimetidine will increase the level or effect of perphenazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • phenobarbital

    phenobarbital will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • phytoestrogens

    cimetidine decreases levels of phytoestrogens by inhibition of GI absorption. Applies only to oral form of both agents. Minor/Significance Unknown.

  • piroxicam

    cimetidine will increase the level or effect of piroxicam by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • primidone

    primidone will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • prochlorperazine

    cimetidine will increase the level or effect of prochlorperazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • promazine

    cimetidine will increase the level or effect of promazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • promethazine

    cimetidine will increase the level or effect of promethazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • ramelteon

    cimetidine will increase the level or effect of ramelteon by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • rifampin

    rifampin will decrease the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.

  • riluzole

    cimetidine will increase the level or effect of riluzole by affecting hepatic enzyme CYP1A2 metabolism. Minor/Significance Unknown.

  • risperidone

    cimetidine will increase the level or effect of risperidone by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • sulfamethoxazole

    cimetidine will increase the level or effect of sulfamethoxazole by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • tolterodine

    cimetidine will increase the level or effect of tolterodine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • trifluoperazine

    cimetidine will increase the level or effect of trifluoperazine by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • tropisetron

    cimetidine will increase the level or effect of tropisetron by affecting hepatic enzyme CYP2D6 metabolism. Minor/Significance Unknown.

  • varenicline

    cimetidine increases levels of varenicline by decreasing renal clearance. Minor/Significance Unknown.

  • voriconazole

    voriconazole will increase the level or effect of cimetidine by affecting hepatic enzyme CYP2C19 metabolism. Minor/Significance Unknown.cimetidine will increase the level or effect of voriconazole by affecting hepatic enzyme CYP2C9/10 metabolism. Minor/Significance Unknown.

  • Премиум таблетки антацид HB200 200 мг, 30 штук для облегчения жжения и изжоги в желудке Tagamet

    Артикул: 6279988

    Цвет: Нет цвета (no color)

    Описание товара

    Рус Eng

    Переведено автоматически

    Срок годности: 06/2026

    • Таблетки циметидина 200 мг
    • Всего одна таблетка для облегчения
    • Снимает и предотвращает изжогу и кислотное расстройство
    • 30 доз

    Применение:

    • Перед едой
    • Во время еды
    • После еды

    Советы по контролю изжоги:

    • Не ложитесь горизонтально и не наклоняйтесь сразу после еды
    • Не ешьте поздно ночью или прямо перед сном
    • Некоторые продукты или напитки могут вызывать изжогу, такие как жирные, острые, жареные блюда, шоколад, кофеин, алкоголь, а также некоторые фрукты и овощи
    • Ешьте медленно и избегайте больших порций
    • Если у вас избыточный вес, постарайтесь похудеть
    • Если вы курите, бросьте курить
    • Поднимите изголовье вашей кровати
    • Носите свободную одежду вокруг живота

    Использование:

    • Снимает изжогу, связанную с кислотным расстройством и кислым желудком
    • Предотвращает изжогу, вызванную приемом определенных продуктов и напитков

    Рекомендованное использование:

    Взрослым и детям старше 12 лет:

    • Для облегчения симптомов проглотите 1 таблетку с стаканом воды
    • Для предотвращения симптомов проглотите 1 таблетку с стаканом воды за 30 минут до еды или напитков, вызывающих изжогу

    Не принимать более 2 таблеток за 24 часа.

    Детям младше 12 лет: проконсультируйтесь с врачом.

    Есть вопрос? Напишите в чат

    • Все Нарушение пищеварения и повышенная кислотность Tagamet Категория и бренд
    • Tagamet Все товары Tagamet Бренд
    • Все Нарушение пищеварения и повышенная кислотность Категория

    Описание

    • циметидин, таблетки, 200 мг
    • Всего одна таблетка
    • Облегчает и предотвращает изжогу и кислотное несварение
    • 30 порций

    Принимайте в любое время, когда вам это нужно:

    • Перед едой
    • Во время еды
    • После еды

    Советы по избавлению от изжоги

    • Не ложитесь спать и не наклоняйтесь сразу после еды
    • Не ешьте поздно вечером или непосредственно перед сном.
    • Некоторые продукты или напитки, например, жирная, пряная, жирная и жареная пища, шоколад, кофеин, алкоголь и даже некоторые фрукты и овощи, могут с большей вероятностью вызвать изжогу.
    • Ешьте медленно и не ешьте большими порциями
    • Если у вас избыточный вес, похудейте
    • Если вы курите, бросьте курить
    • Поднимите изголовье кровати
    • Носите свободную одежду, закрывающую живот.

    Назначение

    • Уменьшает изжогу, вызванную кислотным несварением и кислотностью в желудке
    • Предотвращает изжогу, связанную с несварением кислоты и кислотностью в желудке, вызванных употреблением определенных продуктов питания и напитков

    Рекомендации по применению

    Взрослым и детям старше 12 лет:

    • Для облегчения симптомов принимать 1 таблетку, запивая стаканом воды.
    • Для предотвращения симптомов принимайте 1 таблетку, запивая стаканом воды, непосредственно перед или в любое время за 30 минут до еды или напитков, вызывающих изжогу.

    Не принимайте более 2 таблеток в течение 24 часов.

    Дети в возрасте до 12 лет: необходимо проконсультироваться с врачом.

    Ингредиенты

    Сведения о действующих веществах
    Активный ингредиент (в каждой таблетке) Назначение
    Циметидин, 200 мг Подавитель кислоты
    Вспомогательные ингредиенты
    Целлюлоза, кукурузный крахмал, гипромеллоза, стеарат магния, полиэтиленгликоль, полисорбат 80, повидон, лаурилсульфат натрия, крахмалгликолят натрия, диоксид титана.

    Предупреждения

    Предупреждение об аллергенах. Не используйте, если у вас аллергия на циметидин или другие препараты, снижающие кислотность.

    Не использовать

    • Если у вас есть проблемы или боль при глотании пищи, рвота с кровью, кровавый или черный стул. Это могут быть признаки серьезного заболевания. Обратитесь к врачу.
    • с другими агентами, снижающими кислотность

    Проконсультируйтесь с врачом перед использованием в таких случаях:

    • частая боль в груди
    • частые хрипы, особенно при изжоге
    • необъяснимое снижение веса
    • тошнота или рвота , боль в желудке .
    • изжога в течение 3 месяцев. Это может быть признаком более серьезного состояния.
    • Изжога с головокружением, потливостью или головокружением. Боль в груди или боль в плече с одышкой. потливость; боль, которая распространяется на руки, шею или плечи; легкости или головокружения;
    • Болезнь почек, болезнь печени

    Проконсультируйтесь с врачом или фармацевтом перед использованием, если вы принимаете:

    • рецептурных препаратов. Понижающие кислотность продукты могут взаимодействовать с некоторыми рецептурными препаратами.

    Прекратите использование и проконсультируйтесь с врачом в указанных ниже случаях.

    • вам необходимо принимать этот продукт более 14 дней.
    • боль в желудке не проходит
    • изжога не проходит или усиливается.

    Перед применением во время беременности или кормления грудью следует проконсультироваться с медицинским работником. Хранить в недоступном для детей месте. В случае передозировки обратитесь за медицинской помощью или немедленно свяжитесь с токсикологическим центром.

    Хранить при температуре 15–30 ℃ (59–86 ºF).

    Сохраните упаковку для получения полной информации.

    Продукт имеет защиту от вскрытия. Каждая таблетка запечатана в отдельный блистер. Не используйте, если блистер или фольга открыты или повреждены.

    Отказ от ответственности

    Компания «Eco-Herb» всегда стремится придерживаться максимальной точности в изображениях и информации о своей продукции. Однако некоторые изменения, вносимые производителями, касающиеся упаковки или списка ингредиентов, могут потребовать определенного времени до того момента, как они будут опубликованы на сайте. Имейте в виду, что даже несмотря на то, что иногда упаковка товаров может изменяться, это никак не влияет на качество и свежесть продуктов. Мы рекомендуем вам внимательно ознакомиться с данными на упаковке, предупреждениями и инструкциями по использованию продуктов перед их применением и не полагаться исключительно на информацию, представленную на сайте «Eco-Herb».
    Обратите внимание, что некоторые из описаний продуктов на нашем сайте выполнены с использованием машинного перевода. Это сделано исключительно для вашего удобства. «Eco-Herb» не гарантирует, что переводы являются полными и безошибочными, и не несет ответственности за ошибки или неточности при переводе.

    Оплата

    Вы можете оплатить ваш заказ в рублях по безналичному расчету (пластиковые карты VISA/MasterCard/МИР). Мы работаем по 100% предоплате.

    Доставка

    Способ доставки

     

    Почта России

    Boxberry

     
    Почтовое отделение
    Курьерская доставка
    ПВЗ
    Курьерская доставка
    Описание
    Посылка отправляется ТК из США, до Почты России в Германии. Посылке присваивается трек-номер для отслеживания, который отправляется на Вашу электронную почту Посылка отправляется ТК из США, до Почты России в Германии. Посылке присваевается трек-номер для отслеживания, который отправляется на Вашу электронную почту. После прибытия посылки в службу курьерской доставки Почты России, ее доставит курьер до Вашего адреса. Заказы передаются в транспортную компанию, которая доставляет посылки из США, через Узбекистан и до РФ. Далее, после прохождения таможенного контроля посылки отправляются в транспортную компанию Boxberry. Посылке присваивается трек-номер для отслеживания, который отправляется на Вашу электронную почту. Заказы передаются в транспортную компанию, которая доставляет посылки из США, через Узбекистан и до РФ. Далее, после прохождения таможенного контроля посылки отправляются в транспортную компанию Boxberry. Посылке присваивается трек-номер для отслеживания, который отправляется на Вашу электронную почту.После прибытия посылки в службу курьерской доставки Boxberry, ее доставит курьер до Вашего адреса.
    Срок доставки ТК
    14-25 дней 14-30 дней

    20-30 дней

    Срок доставки от момента поступления посылки на склад Boxberry, 2-3 рaбочих дня, выходные и прaздничные дни не считaются.

    20-30 дней

    Срок доставки от момента поступления посылки на склад Boxberry, 2-3 рaбочих дня, выходные и прaздничные дни не считaются. Для курьерской достaвки срок увеличивaется нa 1 день.

    Стоимость
    Бесплатно 500,00 ₽ Стоимость доставки будет рассчитана при оформлении заказа. 500,00 ₽
    Отслеживание

    На сайте Почты России: https://www.pochta.ru

    Трек-номер будет работать после прохождения таможенной службы в РФ.

    На сайте Почты России: https://www.pochta.ru

    Трек-номер будет работать после прохождения таможенной службы в РФ.

    На сайте Boxberry: https://boxberry.ru

    Для этого вaм не понaдобится регистрaция. Достaточно ввести трек-номер для отслеживaния и нaжaть кнопку «Отследить». Отследить посылку в мобильном приложении или в личном кaбинете.

    Трек-номер будет работать после прохождения таможенной службы в РФ и поступления посылки на склад Boxberry, до этого посылку везет другая ТК.

    На сайте Boxberry: https://boxberry.ru

    Для этого вaм не понaдобится регистрaция. Достaточно ввести трек-номер для отслеживaния и нaжaть кнопку «Отследить». Отследить посылку в мобильном приложении или в личном кaбинете.

    Трек-номер будет работать после прохождения таможенной службы в РФ и поступления посылки на склад Boxberry, до этого посылку везет другая ТК.

    ВНИМАНИЕ:

    • Для доставки Почтой России, трек-номер будет работать после прохождения таможенной службы в РФ;
    • Для доставки Boxberry, трек-номер будет работать после прохождения таможенной службы в РФ и поступления посылки на склад Boxberry, до этого посылку везет другая ТК.
    • Доставка в Крым на данный момент не осуществляется.

    Лимит беспошлинного ввоза в РФ — 200 евро на одну посылку.

    Состав

    В состав препарата входит действующее вещество циметидин и дополнительные компоненты: магния стеарат, повидон, крахмал кукурузный, целлюлоза микрокристаллическая, тальк и так далее.

    Форма выпуска

    Выпускается Циметидин в форме таблеток. Таблетки расфасованы по 10 штук в ячейковые упаковки, по 10 упаковок в пачке.

    Фармакологическое действие

    Циметидин обладает противоязвенным действием.

    Фармакодинамика и фармакокинетика

    Лекарство является блокатором гистаминовых Н2-рецепторов I поколения. При его приеме подавляется выработка соляной кислоты, повышается рН, что позволяет снизить активность пепсина.

    Лечение Циметидином способствует восстановлению защитных механизмов слизистой желудка и заживлению различных повреждений, вызванных влиянием соляной кислоты. Происходит это благодаря повышению выработки желудочной слизи, увеличению содержания в ней гликопротеинов, дополнительному стимулированию секреции гидрокарбоната слизистой желудка и так далее.

    Кроме того, отмечено сокращение концентрации восстановленного цитохрома P450, значительное подавление анилингидроксилазной активности микросомальных ферментов печени. При этом препарат не оказывает воздействия на адренорецепторы, не проявляет местноанестезирующий эффект.

    Во время лечения крапивницы происходит блокирование гистаминовых H2-рецепторов в кровеносных сосудах кожных покровов, частично отвечающих за проявление воспалительных реакций. Также для Циметидина характерен антиандрогенный эффект, блокирующий дигидротестостерон, что приводит к транзиторному повышению концентрации Пролактина – когда препарат вводится струйно в/в.

    Развитие терапевтического действия отмечается спустя 1 час, при условии применения 300 мг лекарства, сохраняется не менее 4-5 часов.

    Внутри организма происходит полноценное всасывание из ЖКТ. Метаболизм происходит преимущественно в печени, в результате чего образуются метаболиты: сульфоксид и гидроксиметил циметидина.

    Распределение Циметидина охватывает достаточно широкое пространство в тканях, связь с белками плазмы составляет почти 20%. Выведение препарата происходит при помощи почек, в неизмененном виде.

    Показания к применению

    Как правило, Циметидин назначается при:

    • обострениях язвенной болезни желудка и 12-перстной кишки;
    • симптоматических язвах;
    • эрозивном и рефлюкс-эзофагите;
    • синдроме Золлингера-Эллисона;
    • изжоге, связанной с гиперхлоргидрией;
    • профилактике язвенных обострений, эрозивно-язвенных поражениях верхних отделов ЖКТ, рецидивов кровотечений данной области, послеоперационных осложнений, системного мастоцитоза, полиэндокринного аденоматоза.

    Также препарат может назначаться в качестве дополнительной терапии, например: при недостаточности ферментов поджелудочной железы, острых формах крапивницы, ревматоидном артрите.

    Противопоказания к применению

    Основным противопоказанием к назначению Циметидина является наличие повышенной чувствительности к нему и его компонентам.

    Побочные эффекты

    При лечении Циметидином могут возникать негативные явления, затрагивающие различные органы и системы, например: пищеварительную, нервную, эндокринную, сердечно-сосудистую, мочевыделительную, костно-мышечную и кроветворения.

    Поэтому возможно развитие: тошноты, рвоты, диареи, гепатита, панкреатита, желтухи, сонливости, утомляемости, депрессии, головокружения, нервозности, головной боли, гинекомастии, тахикардии, брадикардии, нефрита, миалгии и так далее.

    Кроме того, могут проявиться различные виды аллергических реакций, к примеру, в виде: кожной сыпи, зуда, гиперемии, ангионевротического отека, многоформной эритемы, эксфолиативного дерматита. Также отмечены случаи выпадения волос.

    Инструкция по применению Циметидина (Способ и дозировка)

    Как сообщает инструкция по применению Циметидина, терапевтическая схема устанавливается индивидуально.

    Взрослым пациентам таблетки и капсулы назначают в средней разовой дозировке 100-800 мг.

    Дозировка препарата в инъекциях составляет 200-400 мг. При продолжительных в/в инфузиях назначают 50-100 мг/ч.

    В любом случае, независимо от вида введения, максимально допустимая суточная доза составляет до 2,4 г – взрослым пациентам.

    Детям от 1 года суточную дозировку Циметидина рассчитывают с учётом массы тела – 25-30 мг/кг, до года – 20 мг/кг.

    Передозировка

    Установлено, что применение препарата в дозировке менее 20 г не приводит к развитию неблагоприятных эффектов.

    В других случаях может возникать: сонливость, тошнота, брадикардия, сухость во рту.

    Лечение включает промывание желудка – в первые 4 часа, если необходимо проводить гемодиализ. Пациентам требуется постоянное наблюдение и симптоматическая терапия.

    Взаимодействие

    Во время применения Циметидина с другими лекарственными средствами проявляются многочисленные лекарственные взаимодействия.

    Особенно необходимо воздержаться от сочетания:

    • с анальгетиками, противоэпилептическими средствами: Карбамазепином, фенитоином и Вальпроатом;
    • с препаратами, влияющими на деятельность сердечно-сосудистой системы: Амиодароном, Флеканидом, Лигнокаином, Прокаинамидом, Пропафеноном, Хинидином, бета-блокаторами, некоторыми блокаторами кальциевых каналов;
    • с антибактериальными средствами: Метронидазолом и Эритромицином (так как Циметидин способен повысить их плазменную концентрацию).

    Прием с антикоагулянтами повышает противосвертывающий эффект Варфарина и Никумалона. Также данный препарат повышает плазменную концентрацию Теофиллина и Циклоспорина.

    Условия продажи

    В аптеке Циметидин можно приобрести по рецепту, выданному врачом.

    Условия хранения

    Лекарство допускается хранить, в прохладном, темном и сухом месте, недоступном детям.

    Срок годности

    4 года.

    Аналоги Циметидина

    Совпадения по коду АТХ 4-го уровня:

    Основные аналоги Циметидина представлены препаратами:

    • Гистодил
    • Цинамет
    • Тагамет
    • Беломет
    • Примамет
    • Альтрамет
    • Циметигет
    • Безидин
    • Цимедал
    • Гастромет
    • Симетидин
    • Циметар
    • Супрамет
    • Таметин
    • Ульцедон
    • Ульцератил
    • Улькомет
    • Загастрол
    • Симесан
    • Нейтронорм
    • Улькометин
    • Цимегексал

    Алкоголь

    При лечении Циметидином от употребления любых алкогольсодержащих средств нужно отказаться. Подобные комбинации способны усилить эффект алкоголя и повысить его содержание в составе крови.

    Отзывы о Циметидине

    Следует отметить, что отзывы о Циметидине в сети встречаются достаточно редко. Дело в том, что, несмотря на высокую эффективность препарата, пациенты отказываются начинать лечение из-за возможного развития многочисленных побочных эффектов или возникновения лекарственного взаимодействия.

    Как рассказывают специалисты, этот препарат можно действительно отнести к эффективным, а побочные эффекты развиваются только в редких случаях. Тем не менее, в клинической практике они предпочитают использовать другие, более современные средства.

    Цена Циметидина, где купить

    Цена Циметидина в российских аптеках варьируется в пределах 300 рублей за упаковку, в зависимости от формы выпуска и объема препарата.

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