The usual dose is 40 mg daily with amoxycillin 1.5 g (750 mg b.d.) for 2 weeks. Up to 2 g/day of amoxycillin has been used in clinical trials.

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Name Gasec - 2 Gastrocaps Composition Gasec-20 Gastrocaps Each Gastrocaps contains: Omeprazole 20 mg (in the form of enteric-coated pellets) Properties, effects Proton Pump Inhibitor Omeprazole belongs to the group of proton pump inhibitors, and inhibits both the basal and stimulated secretion of stomach acid and reduces the amount of pepsin. The duration of effect for stimulated and non-stimulated acid secretion is at least 24 hours. Reduction in acid secretion excludes a major aggressive factor in the pathogenesis of peptic ulcers and other gastrointestinal disorders, leading to relief of pain and to accelerated healing of the mucous membrane defect. Pharmacokinetics Gasec-20 Gastrocaps contain an enteric-coated pellet formulation of omeprazole (because omeprazole is acid-labile, so that absorption of omeprazole only begins after the pellets leave the stomach. Absorption is rapid after oral intake on an empty stomach), with peak plasma levels occurring within 0.5 to 3.5 hours. Absorption may be delayed by food. The plasma half-life is 0.5 to 1 hour. Omeprazole has a limited volume of distribution of 0.3-0.4 l/kg and is initially confined to extracellular fluids; plasma protein binding is approximately 95%. Following absorption, omeprazole is almost completely metabolized in the liver and rapidly eliminated, mostly in the urine. Although the elimination half-life from plasma is short reported to be about 0.5 to 3 hours, its duration of action with regard to acid secretion is much longer, allowing it to be used in single daily doses. Distribution is rapid, and by 4 hours is limited to gastric mucosa, liver and gallbladder. After 48 hours, omeprazole remains only in the gastric mucosa. Passage across the blood-brain barrier appears to be limited. Following single-dose oral administration, the major part of the dose (about 77%) is eliminated in urine as at least six metabolites. Two have been identified as hydroxymeprazole and the corresponding carboxylic acid. The remainder of the dose is recoverable in faeces. This implies considerable biliary excretion of the metabolites of omeprazole. Three metabolites have been identified in plasma - the sulphide and sulphone derivatives of omeprazole. These metabolites have little or no antisecretory activity. In patients with chronic hepatic disease, the bioavailability increases to approximately 100% compared to an IV dose, reflecting decreased first-pass effect, and the plasma half-life of the drug increases to nearly 3 hours compared to the half-life in normal subjects of 0.5-1 hour. In patients with chronic renal impairment, there is a slight increase in bioavailability. Because urinary excretion is a primary route of omeprazole metabolites, their elimination slows in proportion to the decreased creatinine clearance and their concentration increases.

Indications Gasac-20 is used in conditions in which acid reduction is appropriate, with once-daily administration: - Gastroduodenal ulceration: peptic ulcer; duodenal ulcer, benign stomach ulcer, relapsing ulcer, including NSAID-induced peptic ulcer; peptic ulcer after surgery; duodenal ulcer associated with Helicobacter pylori. - Gastritis - Hyper acidic, irritable stomach - Gastroesophageal reflux - Bleeding from ulcerations or erosions in the oesophagus, stomach or duodenum. - Prophylaxis against ulceration and bleeding in the upper gastrointestinal tract in risk patients. - Acute mucosal stress ulceration. - Aspiration syndrome. - Zollinger-Ellison Syndrome. Dosage, application usual dosage Duodenal ulcers, benign gastric ulcers, postoperative ulcers, recurring ulcers: - For short-term management the normal daily dose is 20 mg increasing to 40 mg once daily in severe or refractory cases. A single daily dose of 20 mg before breakfast or before the evening meal produces effective gastric suppression for 16 to 18 hours. This dose can be doubled when the response is not satisfactory. - Duration of treatment. Duodenal ulcer: at least 4 weeks.. Gastric ulcer: at least 6-8 weeks Duodenal ulcer associated with Helicobacter pylori: The usual dose is 40 mg daily with amoxycillin 1.5 g (750 mg b.d.) for 2 weeks. Up to 2 g/day of amoxycillin has been used in clinical trials. Gastroesophageal reflux / erosive oesophagitis: - Usual daily dosage: 20 mg to 40 mg. depending on the severity of the lesion. - Duration of treatment: 4 to 8 weeks, depending on the severity of the lesion. At the beginning of treatment, and in case of continuing pain, antacids may be prescribed. Both in recurrent peptic ulcer and chronic gastroesophageal reflux, pulsed maintenance treatment giving 20 mg of omeprazole for 3 days each week, instead of continuous H2-blocker maintenance therapy, is a promising alternative.

Gastritis, hyperacidity: - The current recommended adult dosage is 20-40 mg twice a day. - Duration of treatment: 1-2 weeks is usually sufficient. Aspiration syndrome: 40 mg given the night before and again on the morning of elective caesarian section effectively increases gastric ph and reduces gastric volume. Zollinger-Ellison Syndrome: Daily dosage 60 mg. Dosages should be adjusted to individual patient needs and should continue as long as clinically indicated. A dosage range of 20 mg to 120 mg/day may be employed depending on the severity of the disease. Dosages of up to 360 mg/day have been employed in patients with severe disease. With doses in excess of 80 mg daily, the dose should be equally divided and given twice daily. Special dosage Instructions Gasec-20 will be most effective when taken with or shortly before meals; effectiveness is likely to be significantly compromised if taken during a prolonged fasting period. Gasec-20 should not be co-administered with another antisecretory agent. Higher dosages or more frequent administration is indicated if greater antisecretory effectiveness is required. Renal impairment: No dose adjustment is needed. Hepatic impairment: The dose should be adjusted; maximum daily dose is 20 mg. In most subjects, the 20 mg dosage will not become fully effective until after about four days of therapy. Continuing H2-blockers will be counter-productive. In the elderly, safety and efficacy appear similar to those of younger age. Restrictions of use / Contraindications There are no known contraindications to the use of Gasec-20. Precautions (1) Stomach ulcers: it is advisable to establish the benign nature of the ulcer before any treatment. Complaints caused by carcinoma of the stomach can be alleviated by omeprazole, and non-

diagnosed carcinomas, in particular early carcinomas, may appear to heal initially with omeprazole therapy. Therefore, the diagnosis and healing of a stomach ulcer must be checked endoscopically and by biopsy. (2) Helicobacter pylori is associated with hyperacidity and peptic ulcer disease, contributing to gastritis and ulcer recurrence. In patients known to be allergic to amoxycillin, clarithromycin may be a useful alternative in dual therapy. Omeprazole 40 mg daily, amoxycillin 1500 mg daily and metronidazole 1200 mg daily for 14 days achieved an overall Helicobacter eradication rate of 89% to 96%. (3) Pregnancy, lactation. There are no adequate or well-controlled studies in pregnant women and Gasec-20 should only be used when potential benefits outweigh the potential hazards to the fetus. It is not known whether omeprazole is excreted in human milk. Because of the potential for serious adverse reactions in nursing infants from omeprazole, and because of the potential for tumorigenicity shown for omeprazole in rat carcinogenicity studies, patients taking omeprazole should not breast feed. (4) Paediatric use: Safety and effectiveness in children have not been established. Side effects Gasec-20 is a drug with a very low incidence of minor side effects and is generally well tolerated. Occasionally, nausea, vomiting, diarrhoea, constipation, flatulence, abdominal pain, skin disorders, have been reported. These events have been transient and usually mild. Liver enzyme changes, haematological changes, angioedema, fatigue, paraesthesia, insomnia, muscle and joint pains, have also been reported, but are rare, and there has been no consistent relationship with treatment. Interactions Gasec-20 can prolong the elimination of diazepam, phenytoin and warfarin, drugs that are metabolized by oxidation in the liver by subsets of the cytochrome P-450 enzyme system. This effect is minor at clinically relevant doses. However, monitoring of patients also receiving warfarin or phenytoin is recommended and a reduction of dose of phenytoin and warfarin may be necessary. No interaction with propranolol or theophylline has been found, but interactions with other drugs also metabolized via the cytochrome P-450 enzyme system cannot be excluded. No interaction with concomitantly administered antacids has been found. Storage Store dry below 30? C. Keep out of reach of children. Presentation Packings of 7 and 14 Gastrocaps. Company Manufactured by: Medical Union Pharmaceuticals (MUP), Abu Sultan - Ismailia - Egypt In Cooperation with: Mepha Pharma Egypt S.A.E.

Under Supervision of: Mepha Ltd, Basel - Switzerland