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Топ 20 лекарств с такими-же компонентами:
Treatment Of Gastroesophageal Reflux Disease (GERD)
Healing Of Erosive Esophagitis
Esomepra is indicated for the short-term treatment (4 to 8 weeks) in the healing and symptomatic resolution of diagnostically confirmed erosive esophagitis. For those patients who have not healed after 4 to 8 weeks of treatment, an additional 4 to 8 week course of Esomepra may be considered.
In infants 1 month to less than 1 year, Esomepra is indicated for short-term treatment (up to 6 weeks) of erosive esophagitis due to acid-mediated GERD.
Maintenance Of Healing Of Erosive Esophagitis
Esomepra is indicated to maintain symptom resolution and healing of erosive esophagitis. Controlled studies do not extend beyond 6 months.
Symptomatic Gastroesophageal Reflux Disease
Esomepra is indicated for short-term treatment (4 to 8 weeks) of heartburn and other symptoms associated with GERD in adults and children 1 year or older.
Risk Reduction Of NSAID-Associated Gastric Ulcer
Esomepra is indicated for the reduction in the occurrence of gastric ulcers associated with continuous NSAID therapy in patients at risk for developing gastric ulcers. Patients are considered to be at risk due to their age ( ≥ 60) and/or documented history of gastric ulcers. Controlled studies do not extend beyond 6 months.
H. pylori Eradication To Reduce The Risk Of Duodenal Ulcer Recurrence
Triple Therapy (Esomepra plus amoxicillin and clarithromycin): Esomepra, in combination with amoxicillin and clarithromycin, is indicated for the treatment of patients with H. pylori infection and duodenal ulcer disease (active or history of within the past 5 years) to eradicate H. pylori. Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.
In patients who fail therapy, susceptibility testing should be done. If resistance to clarithromycin is demonstrated or susceptibility testing is not possible, alternative antimicrobial therapy should be instituted.
Pathological Hypersecretory Conditions Including Zollinger-Ellis On Syndrome
Esomepra is indicated for the long-term treatment of pathological hypersecretory conditions, including Zollinger-Ellison Syndrome.
Esomepra strontium is used to treat conditions where there is too much acid in the stomach. It is used to treat duodenal and gastric ulcers, erosive esophagitis, gastroesophageal reflux disease (GERD), and the Zollinger-Ellison syndrome. Esomepra is also used with antibiotics (eg, amoxicillin, clarithromycin) to treat ulcers that are caused by the H. pylori bacteria. Esomepra strontium is also used to prevent stomach ulcers and stomach irritation in patients taking pain and arthritis drugs called NSAIDs, such as aspirin or ibuprofen, for long periods of time.
Esomepra strontium is a proton pump inhibitor (PPI). It works by decreasing the amount of acid that is produced by the stomach.
Esomepra strontium is available only with your doctor’s prescription.
Usual Adult Dose for Gastroesophageal Reflux Disease:
Esomepra Magnesium:
-20 mg orally once a day for 4 weeks
Esomepra Strontium:
-24.65 mg orally once a day for 4 to 8 weeks.
Comment:
-If symptoms do not resolve after 4 weeks, an additional 4 weeks may be considered.
GERD with Erosive Esophagitis:
Esomepra Sodium:
-20 mg or 40 mg IV injection once a day, over no less than 3 minutes; or IV infusion once a day, over no less than 10 to 30 minutes
Comment: Safety and efficacy of Esomepra sodium IV for Injection for more than 10 days have not been demonstrated.
Uses: Short term treatment of heartburn and symptomatic gastroesophageal reflux disease; short term treatment of GERD with erosive esophagitis, inclusively as an alternative to oral therapy, if unable to use oral route
Usual Adult Dose for Erosive Esophagitis:
Healing:
-Esomepra Magnesium: 20 to 40 mg orally once a day for 4 to 8 weeks
-Esomepra Strontium: 24.65 to 49.3 mg orally once a day for 4 to 8 weeks
-An additional 4 to 8 week course of therapy may be considered in patients not healed after initial treatment.
Maintenance of healing:
-Esomepra Magnesium: 20 mg orally once a day
-Esomepra Strontium: 24.65 mg orally once a daily
Comments:
-Esomepra Sodium injection may be used as an alternative to oral therapy, if unable to use oral route.
-Maintenance of healing: Controlled studies did not extend beyond six months.
Uses: Short-term treatment in the healing and symptomatic resolution of diagnostically confirmed erosive esophagitis; to maintain symptom resolution and healing of erosive esophagitis
Usual Adult Dose for Helicobacter pylori Infection:
Esomepra Magnesium:
Triple therapy:
-40 mg orally once a day for 10 days, along with amoxicillin 1000 mg and clarithromycin 500 mg orally twice a day for 10 days
Esomepra Strontium:
Triple therapy:
-49.3 mg orally once a day for 10 days, along with amoxicillin 1000 mg and clarithromycin 500 mg orally twice a day for 10 days
Comments:
-Susceptibility testing should be done in patients who fail therapy.
-If resistance to clarithromycin is demonstrated or susceptibility testing is not possible, alternative antimicrobial therapy should be instituted.
-Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.
Use: Triple therapy (Esomepra plus amoxicillin and clarithromycin): Treatment of H. pylori infection and duodenal ulcer disease (active or history of within the past 5 years) to eradicate H. pylori
Usual Adult Dose for NSAID-Induced Gastric Ulcer:
Esomepra Magnesium:
-20 mg to 40 mg orally once daily for up to 6 months
Esomepra Strontium:
-24.65 mg to 49.3 mg orally once a day for up to 6 months
Comment:
-Patients older than 60 years and/or with history of gastric ulcers are considered to be at risk for developing gastric ulcers.
-Controlled studies do not extend beyond 6 months
Use: Reduction in the occurrence of gastric ulcers associated with continuous NSAID therapy in patients at risk for developing gastric ulcers.
Usual Adult Dose for Zollinger-Ellison Syndrome:
Esomepra Magnesium:
-40 mg orally twice a day
Esomepra Strontium:
-49.3 mg orally twice a day
Comment: Doses up to 240 mg daily have been used.
Use: Long term treatment of pathological hypersecretory conditions, including Zollinger-Ellison Syndrome
Usual Adult Dose for Pathological Hypersecretory Conditions:
Esomepra Magnesium:
-40 mg orally twice a day
Esomepra Strontium:
-49.3 mg orally twice a day
Comment: Doses up to 240 mg daily have been used.
Use: Long term treatment of pathological hypersecretory conditions, including Zollinger-Ellison Syndrome
Usual Adult Dose for Duodenal Ulcer Prophylaxis:
Esomepra Sodium:
-Initial dose: 80 mg IV infusion over 30 minutes
-Maintenance dose: 8 mg/hr IV continuous infusion for a total of 72 hours (includes initial 30 minute dose plus 71.5 hours of continuous infusion)
Comments:
-Intravenous therapy is aimed solely at the acute initial management of bleeding gastric or duodenal ulcers and does not constitute full treatment.
-Intravenous therapy should be followed by oral acid-suppressive therapy.
Use: Risk reduction of rebleeding of gastric or duodenal ulcers following therapeutic endoscopy
Usual Adult Dose for Gastric Ulcer Prophylaxis:
Esomepra Sodium:
-Initial dose: 80 mg IV infusion over 30 minutes
-Maintenance dose: 8 mg/hr IV continuous infusion for a total of 72 hours (includes initial 30 minute dose plus 71.5 hours of continuous infusion)
Comments:
-Intravenous therapy is aimed solely at the acute initial management of bleeding gastric or duodenal ulcers and does not constitute full treatment.
-Intravenous therapy should be followed by oral acid-suppressive therapy.
Use: Risk reduction of rebleeding of gastric or duodenal ulcers following therapeutic endoscopy
Usual Pediatric Dose for Gastroesophageal Reflux Disease:
Esomepra Magnesium:
Less than 1 year:
-Data not available
1 to 11 years:
-10 mg once a day for up to 8 weeks
-Comment: Doses over 1 mg/kg/day have not been studied.
12 to 17 years:
-20 mg once a day for 4 weeks
Esomepra Sodium:
GERD with Erosive Esophagitis:
Less than 1 month:
-Not recommended.
1 month to less than 1 year:
-0.5 mg/kg IV infused over 10 to 30 minutes
1 to 17 years:
-Less than 55 kg: 10 mg IV infused over 10 to 30 minutes
-55 kg or more: 20 mg IV infused over 10 to 30 minutes
Esomepra Strontium: Not recommended.
Uses: Short term treatment of symptomatic GERD; short term treatment of GERD with erosive esophagitis, inclusively as an alternative to oral therapy, if unable to use oral route
Usual Pediatric Dose for Erosive Esophagitis:
Esomepra Magnesium:
Healing:
Less than 1 year:
-Data not available
1 to 11 years:
-Less than 20 kg: 10 mg once a day for 8 weeks
-20 kg or more: 10 mg or 20 mg once a day for 8 weeks
12 to 17 years:
-20 or 40 mg once a day for 4 to 8 weeks
Comment: Doses over 1 mg/kg/day have not been studied.
Erosive Esophagitis due to acid-mediated GERD:
Less than 1 month:
-Data not available
1 month to less than 1 year old:
-3 kg to 5 kg: 2.5 mg once a day
-Greater than 5 kg to 7.5 kg: 5 mg once a day
-Greater than 7.5 kg to 12 kg: 10 mg once a day
Duration of therapy: For up to 6 weeks
Comment: Doses over 1.33 mg/kg/day have not been studied.
1 year and older:
-Data not available
Uses: Short-term treatment in the healing and symptomatic resolution of diagnostically confirmed erosive esophagitis; short term treatment of erosive esophagitis due to acid-mediated GERD in infants
See also:
What is the most important information I should know about Esomepra?
Esomepra is rapidly absorbed after oral doses, with peak plasma levels occurring after about 1-2 hrs. It is acid labile and an enteric-coated formulation has been developed. Bioavailability of Esomepra increases with both dose and repeated administration to about 68% and 89% for doses of 20 mg and 40 mg, respectively. Food delays and decreases the absorption of Esomepra, but this does not significantly change its effect of intragastric acidity. Esomepra is about 97% bound to plasma proteins. It is extensively metabolized in the liver by the cytochrome P450 (CYP450) isoenzyme CYP2C19 to hydroxy and desmethyl metabolites, which have no effect on gastric acid section. The remainder is metabolized by the CYP450 isoenzyme CYP3A4 to Esomepra sulfone. With repeated dosage, there is a decrease in first-pass metabolism and systemic clearance, probably caused by an inhibition of the CYP2C19 isoenzyme. However, there is no accumulation during once daily use. The plasma elimination half-life (t½) is about 1.3 hrs. Almost 80% of an oral dose is eliminated as metabolites in the urine, the remainder in the feces.
Use Esomepra suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.
- Esomepra suspension comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Esomepra suspension refilled.
- Take Esomepra suspension by mouth on an empty stomach at least 1 hour before a meal.
- You will need to mix Esomepra suspension in a small amount of water before taking your dose. You should use an oral syringe to measure the amount of water needed to mix your dose. Ask your pharmacist for an oral syringe. The recommended amount of water for the mixing of each dose is as follows:
- If your dose of Esomepra suspension is 2.5 or 5 mg, add 1 teaspoon (5 mL) of water to a container.
- If your dose of Esomepra suspension is 10, 20, or 40 mg, add 1 tablespoon (15 mL) of water to a container
- Tear open the medicine packet and add the contents of the packet to the container. Stir well. Allow the mixture to thicken for 2 to 3 minutes. Stir again. Drink the mixture within 30 minutes. If it is not used within 30 minutes, throw away this dose and mix a new dose. If any medicine remains in the glass after drinking, add more water. Stir and then drink right away.
- If the patient is taking Esomepra suspension through a nasogastric (NG) tube or gastric tube, follow the instructions for use in the extra patient leaflet.
- If your doctor has instructed you to use more than 1 packet for your dose, follow the mixing instructions provided by your doctor or pharmacist.
- You may take antacids while you are using Esomepra suspension if you are directed to do so by your doctor.
- Continue to take Esomepra suspension even if you feel well. Do not miss any doses.
- If you miss a dose of Esomepra suspension, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.
Ask your health care provider any questions you may have about how to use Esomepra suspension.
There are specific as well as general uses of a drug or medicine. A medicine can be used to prevent a disease, treat a disease over a period or cure a disease. It can also be used to treat the particular symptom of the disease. The drug use depends on the form the patient takes it. It may be more useful in injection form or sometimes in tablet form. The drug can be used for a single troubling symptom or a life-threatening condition. While some medications can be stopped after few days, some drugs need to be continued for prolonged period to get the benefit from it.Use: Labeled Indications
Oral:
Esomepra magnesium and Esomepra strontium:
Gastroesophageal reflux disease (Rx only):
Healing of erosive esophagitis: Short-term (4 to 8 weeks) treatment of erosive esophagitis
Maintenance of healing of erosive esophagitis: Maintaining symptom resolution and healing of erosive esophagitis
Symptomatic gastroesophageal reflux disease: Short-term (4 to 8 weeks) treatment of symptomatic gastroesophageal reflux disease (GERD)
Helicobacter pylori eradication (Rx only): As part of a multidrug regimen for Helicobacter pylori eradication in patients with duodenal ulcer disease (active or history of within the past 5 years)
Risk reduction of nonsteroidal anti-inflammatory drug-associated gastric ulcer (Rx only): Prevention of gastric ulcers associated with continuous NSAID therapy in patients at risk (age ≥60 years and/or history of gastric ulcer)
Pathological hypersecretory conditions, including Zollinger-Ellison syndrome (Rx only): Treatment (long-term) of pathological hypersecretory conditions including Zollinger-Ellison syndrome
Esomepra magnesium:
Heartburn (OTC labeling): Treatment of frequent heartburn (≥2 days per week).
IV: Esomepra sodium:
Gastroesophageal reflux disease (Rx only): Short-term (≤10 days) treatment of gastroesophageal reflux disease (GERD) with erosive esophagitis in pediatric patients 1 month to 17 years of age and adults when oral therapy is not possible or appropriate
Risk reduction of ulcer rebleeding postprocedure (Rx only): Decrease the risk of rebleeding postendoscopy for acute bleeding gastric or duodenal ulcers in adults
Off Label Uses
Barrett esophagus
Data from a meta-analysis of observational studies evaluating acid suppressive therapy and the risk of esophageal adenocarcinoma or high-grade dysplasia in patients with Barrett esophagus showed that proton pump inhibitors were associated with a reduction in the risk of esophageal adenocarcinoma and high-grade dysplasia associated with Barrett esophagus; a longer duration of PPI use was associated with a greater protective effect.
See also:
What other drugs will affect Esomepra?
Esomepra is extensively metabolized in the liver by CYP2C19 and CYP3A4.
In vitro and in vivo studies have shown that Esomepra is not likely to inhibit CYPs 1A2, 2A6, 2C9, 206, 2E1 and 3A4. No clinically relevant interactions with drugs metabolized by these CYP enzymes would be expected. Drug interaction studies have shown that Esomepra does not have any clinically significant interactions with phenytoin, warfarin, quinidine, clarithromycin or amoxicillin. Post-marketing reports of changes in prothrombin measures have been received among patients on concomitant warfarin and Esomepra therapy. Increases in INR and prothrombin time may lead to abnormal bleeding and even death. Patients treated with proton pump inhibitors and warfarin concomitantly may need to be monitored for increases in INR and prothrombin time.
Esomepra may potentially interfere with CYP2C19, the major Esomepra metabolizing enzyme. Coadministration of Esomepra 30 mg and diazepam, a CYP2C19 substrate, resulted in a 45% decrease in clearance of diazepam. Increased plasma levels of diazepam were observed 12 hours after dosing and onwards. However, at that time, the plasma levels of diazepam were below the therapeutic interval, and thus this interaction is unlikely to be of clinical relevance.
Concomitant administration of Esomepra and a combined inhibitor of CYP2C19 and CYP3A4, such as voriconazole, may result in more than doubling of the Esomepra exposure. Dose adjustment of Esomepra is not normally required for the recommended doses. However, in patients who may require higher doses, dose adjustment may be considered.
Esomepra acts as an inhibitor of CYP2C19. Esomepra given in doses of 40 mg daily for one week to 20 healthy subjects in cross-over study, increased Cmax and AUC of cilostazol by 18% and 26% respectively. Cmax and AUC of one of its active metabolites, 3,4-dihydro-cilostazol, which has 4-7 times the activity of cilostazol, were increased by 29% and 69% respectively. Co-administration of cilostazol with Esomepra is expected to increase concentrations of cilostazol and its above mentioned active metabolite. Therefore a dose reduction of cilostazol from 100 mg b.i.d. to 50 mg b.i.d. should be considered.
Co-administration of' oral contraceptives, diazepam, phenytoin, or quinidine did not seen to change the pharmacokinetic profile of Esomepra.
Antiretroviral Agents: Concomitant use of atazanavir and nelfinavir with proton pump inhibitors is not recommended. Co-administration of atazanavir with proton pump inhibitors is expected to substantially decrease atazanavir plasma concentrations and thereby reduce its therapeutic effect.
Esomepra has been reported to interact with some antiretroviral drugs. The clinical importance and the mechanisms behind these interactions are not always known. Increased gastric pH during Esomepra treatment may change the absorption of the antiretroviral drug. Other possible interaction mechanisms are via CYP2C19. For some antiretroviral drugs, such as atazanavir and nelfinavir, decreased serum levels have been reported when given together with omeprazole. Following multiple doses of nelfinavir (1250 mg, bid) and Esomepra (40 mg qd). AUC was decreased by 36% and 92%, Cmax by 37% and 89% and Cmin by 39% and 75% respectively for nelfinavir and M8. Following multiple doses of atazanavir (400 mg, qd) and Esomepra (40 mg, qd, 2 hr before atazanavir), AUC was decreased by 94%, Cmax by 96%, and Cmin by 95%. Concomitant administration with Esomepra and drugs such as atazanavir and nelfinavir is therefore not recommended. For other antiretroviral drugs, such as saquinavir, elevated serum levels have been reported with an increases in AUC by 82%, in Cmax by 75% and in Cmin by 106% following multiple dosing of saquinavir/ritonavir (1000/100 mg) bid for 15 days with Esomepra 40 mg qd coadministered days 11 to 15. Therefore, clinical and laboratory monitoring for saquinavir toxicity is recommended during concurrent use with Esomepra.
Dose reduction of saquinavir should be considered from the safety perspective for individual patients. There are also some antiretroviral drugs of which unchanged serum levels have been reported when given with Esomepra.
Studies evaluating concomitant administration of Esomepra and either naproxen (non-selective NSAID) or rofecoxib (COX-2 selective NSAID) did not identify any clinically relevant changes in the pharmacokinetic profiles of Esomepra or these NSAIDs.
Esomepra inhibits gastric acid secretion. Therefore, Esomepra may interfere with the absorption of drugs where gastric pH is an important determinant of bioavailability (eg, ketoconazole, iron salts and digoxin).
Смотрите также:
Каковы возможные побочные эффекты Эсомепры?
Клинические испытания Опыт с
Внутривенная Эсомепра
Поскольку клинические испытания проводятся в широко варьирующихся условиях, частота побочных реакций, наблюдаемая в клинических испытаниях лекарственного средства, не может быть напрямую сопоставлена с частотой клинических испытаний другого лекарственного средства и может не отражать показатели, наблюдаемые на практике.
Взрослые
Безопасность внутривенного эзомепры основана на результатах клинических испытаний, проведенных в четырех различных группах населения, включая пациентов с симптоматической ГЭРБ с или без эрозивного эзофагита в анамнезе (n = 199), пациентов с эрозивным эзофагитом (n = 160), здоровых субъектов (n = 204) и пациенты с кровоточащей язвой желудка или двенадцатиперстной кишки (n = 375).
Симптоматические исследования ГЭРБ и ерозийного эзофагита
Данные, описанные ниже, отражают воздействие Esomepra I.V. для инъекций у 359 пациентов. Эсомепра И.В. для инъекций изучался только в активно контролируемых испытаниях. Население было от 18 до 77 лет; 45% мужчин, 52% кавказцев, 17% чернокожих, 3% азиатов, 28% других, и имели эрозивный рефлюкс-эзофагит (44%) или ГЭРБ (56%). Большинство пациентов получали дозы 20 или 40 мг либо в виде инфузии, либо в виде инъекции. Побочные реакции, возникающие у ≥1% пациентов, получавших внутривенную эзомепру (n = 359) в клинических испытаниях, перечислены ниже:
Было обнаружено, что внутривенное лечение Эзомепрой 20 и 40 мг, вводимым в виде инъекции или в виде инфузии, имеет профиль безопасности, аналогичный пероральному введению Эсомепры.
Педиатрический
Было проведено рандомизированное открытое многонациональное исследование для оценки фармакокинетики повторных внутривенных доз Эсомепры один раз в день у педиатрических пациентов в возрасте от 1 месяца до 17 лет включительно. Результаты безопасности соответствуют известному профилю безопасности Esomepra, и неожиданных сигналов безопасности не выявлено [см. Клиническая фармакология (12.3)].
Снижение риска повторного кровотечения язв желудка или двенадцатиперстной кишки у взрослых
Данные, описанные ниже, отражают воздействие Esomepra I.V. для инъекций у 375 пациентов. Эсомепра И.В. для инъекций был изучен в плацебо-контролируемом исследовании. Пациенты были рандомизированы для получения Esomepra I.V. для инъекций (n = 375) или плацебо (n = 389). Население было от 18 до 98 лет; 68% мужчин, 87% кавказцев, 1% чернокожих, 7% азиатов, 4% других, у которых эндоскопически подтвержденное кровотечение из желудка или двенадцатиперстной кишки. После эндоскопического гемостаза пациенты получали либо 80 мг Эсомепры в виде внутривенной инфузии в течение 30 минут с последующей непрерывной инфузией 8 мг в час, либо плацебо в течение общей продолжительности лечения 72 часа. После начального 72-часового периода все пациенты получали пероральный ингибитор протонной помпы (ИПП) в течение 27 дней.
За исключением реакций в месте инъекции, описанных выше, было обнаружено, что внутривенное лечение Эсомепрой, вводимым в виде инъекции или в виде инфузии, имеет профиль безопасности, аналогичный пероральному введению Эсомепры.
Опыт постмаркетинга
Следующие побочные реакции были выявлены во время использования Esomepra после утверждения. Поскольку об этих реакциях сообщается добровольно от населения неопределенного размера, не всегда возможно надежно оценить их частоту или установить причинную связь с воздействием наркотиков.
Отчеты о постмаркетинге - Были спонтанные сообщения о неблагоприятных событиях с использованием Esomepra после маркетинга. Эти отчеты происходили редко и перечислены ниже по системе организма:
Расстройства крови и лимфатической системы: агранулоцитоз, панцитопения; Нарушения зрения: помутнение зрения; Желудочно-кишечные расстройства: панкреатит; стоматит; микроскопический колит; Гепатобилиарные расстройства: печеночная недостаточность, гепатит с желтухой или без нее; Расстройства иммунной системы: анафилактическая реакция / шок; Инфекции и заражения: кандидоз GI; Нарушения обмена веществ и питания: гипомагниемия с или без гипокальциемии и / или гипокалиемия; Опорно-двигательный аппарат и соединительная ткань: мышечная слабость, миалгия, перелом кости; Расстройства нервной системы: печеночная энцефалопатия, нарушение вкуса; Психические расстройства: агрессия, агитация, депрессия, галлюцинации; Почечные и мочевые расстройства: интерстициальный нефрит; Репродуктивная система и нарушения молочной железы: гинекомастия; Респираторный, Нарушения грудной клетки и средостения: бронхоспазм; Заболевания кожи и подкожной клетчатки: алопеция, мультиформная эритема, гипергидроз, светочувствительность, Синдром Стивенса-Джонсона, токсический эпидермальный некролиз (ДЕСЯТЬ, некоторые смертельные).
Другие побочные эффекты, не наблюдаемые с Esomepra, но встречающиеся с омепразолом, можно найти в вкладыше пакета омепразола, раздел «КОНЕЧНЫЕ РЕАКЦИИ».
Каждая таблетка содержит 20 или 40 мг эсомепры (в виде тригидрата магния).
Каждая таблетка содержит эсомепразол в виде гранул с энтеросолюбильным покрытием (MUPS).
Esomepra MUPS является ингибитором протонной помпы. Активным ингредиентом Esomepra MUPS является тригидрат магния Esomepra, замещенный бензимидазол. Эсомепра является S-изомером омепразола. Это оптически стабильно in vivoс незначительным преобразованием в R-изомер. Химическое название ди- (S) -5-метокси-2 - [[4-метокси-3,5-диметил-2-пиридинил) метил] сульфинил] -1H- тригидрат соли магния бензимидазола.
Его молекулярная формула C34H36N6O6S2Mg · 3H2O и имеет молекулярную массу 767,2 (тригидрат).
Вспомогательные вещества / Неактивные ингредиенты: Глицерин моностеарат 40-55, гипролоза, гипромеллоза, оксид железа (Е 172) ,(Таблетка 20 мг, красновато-коричневый CI 77491, желтый, CI 77492) ,(Таблетка 40 мг, красновато-коричневый CI 77491) стеарат магния, этилакрилатный сополимер метакриловой кислоты (1: 1) дисперсия 30 процентов, целлюлоза микрокристаллическая, синтетический парафин, макроголы, полисорбат 80, кросповидон, стеарилфумарат натрия, сахарные сферы (сахароза и кукурузный крахмал) тальк, диоксид титана (Е 171) триэтилцитрат.
Эсомепра 20 мг : Сахароза 28 мг.
Эсомепра 40 мг : Сахароза 30 мг.
Однако мы предоставим данные по каждому действующему веществу