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Patients under intensive care (Important: reports of bezoar formation)Cautions, further information Bezoar formation. Following reports of bezoar formation associated with sucralfate, caution is advised in seriously ill patients, especially those receiving concomitant enteral feeds or those with predisposing conditions such as delayed gastric emptying.


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nausea, vomiting, gas, indigestion; itching, rash; dizziness, drowsiness; sleep problems ( insomnia ); headache; or. back pain. This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.


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To treat duodenal ulcers: Adults—One gram (g) (10 milliliters [mL]) four times a day, taken on an empty stomach for 4 to 8 weeks. Children—Use and dose must be determined by your doctor. For oral dosage form (tablets): To treat duodenal ulcers: Adults—One gram (g) four times a day, taken on an empty stomach for 4 to 8 weeks.


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Sucralfate Oral Suspension contains sucralfate and sucralfate is an α-D-glucopyranoside, β-D-fructofuranosyl-, octakis- (hydrogen sulfate), aluminum complex. Sucralfate Oral Suspension for oral administration contains 1g of sucralfate per 10 mL. Sucralfate Oral Suspension also contains: colloidal silicon dioxide NF, FD&C Red #40, flavor.


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Adjustment of the anti-diabetic treatment dose during the use of sucralfate suspension might be necessary. Special Populations. Chronic Renal Failure and Dialysis Patients. When sucralfate is administered orally, small amounts of aluminum are absorbed from the gastrointestinal tract. Concomitant use of sucralfate with other products that.


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The physician should read the "PRECAUTIONS" section when considering the use of sucralfate oral suspension in pregnant or pediatric patients, or patients of childbearing potential.Duodenal ulcer is a chronic, recurrent disease. While short-term treatment with sucralfate can result in complete healing of the ulcer, a successful course of treatment with sucralfate should not be expected to alter.


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Side Effects. Constipation, dry mouth, upset stomach, gas, and nausea may occur. If any of these effects last or get worse, notify your doctor or pharmacist promptly. Remember that this medication.


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CARAFATE (sucralfate) Suspension 1 g/10 mL is a pink suspension supplied in bottles of 14 fl oz (NDC 58914-170-14). SHAKE WELL BEFORE USING. AVOID FREEZING. Store at controlled room temperature 20-25°C (68-77°F)[see USP]. Aptalis Pharma US, Inc., 100 Somerset Corporate Boulevard, Bridgewater, NJ 08807, USA. Revised: Apr 2014.


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Sucralfate Suspension. What is this medication? SUCRALFATE (SOO kral fate) treats stomach ulcers. It works by helping to form a barrier over the ulcer, which protects it from stomach acid and allows it to heal. This medicine may be used for other purposes; ask your health care provider or pharmacist if you have questions.


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Use sucralfate oral suspension as ordered by your doctor. Read all information given to you. Follow all instructions closely. Take on an empty stomach. Shake well before use. Measure liquid doses carefully. Use the measuring device that comes with sucralfate oral suspension.


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Sucralfate, sold under various brand names, is a medication used to treat stomach ulcers, gastroesophageal reflux disease (GERD), radiation proctitis, and stomach inflammation and to prevent stress ulcers. [3] [4] [5] Its usefulness in people infected by H. pylori is limited. [3] It is used by mouth (for upper GIT ulcers) and rectally (for.


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Sucralfate is used to treat and prevent duodenal ulcers and other conditions as determined by your doctor. It works by forming a barrier or coat over the ulcer. This protects the ulcer from the acid of the stomach, allowing it to heal. Sucralfate contains an aluminum salt.


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Sucralfate is a medication used to treat duodenal ulcers, epithelial wounds, chemotherapy-induced mucositis, radiation proctitis, ulcers in Behcet disease, and burn wounds. Sucralfate exhibits its action by forming a protective layer, increasing bicarbonate production, exhibiting anti-peptic effects, promoting tissue growth, regeneration, and repair. The medication has a relatively safe.


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Deskripsi. SUCRALFATE SUSPENSI 500 MG/5ML bekerja dengan cara berikatan dengan protein positif membentuk lapisan mukus. Lapisan ini secara lokal melindungi lambung dari asam peptik, pepsin, dan garam empedu. Obat ini digunakan untuk pengobatan jangka pendek dan jangka panjang pada tukak lambung dan usus, gastritis kronik dan profilaksis.


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Sucralfate Suspension Description. Sucralfate Oral Suspension contains sucralfate and sucralfate is an α-D-glucopyranoside, β-D- fructofuranosyl-, octakis- (hydrogen sulfate), aluminum complex. Sucralfate Oral Suspension for oral administration contains 1 g of sucralfate per 10 mL. Sucralfate Oral Suspension also contains: colloidal silicon.


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Sucral Suspension is used in the treatment of ulcers in the stomach and intestine. It contains the active ingredient sucralfate which promotes the healing of ulcers by forming a coating over them which acts as a physical barrier. Sucral Suspension is taken one hour before meals preferably at bedtime in the dose and duration advised by the doctor.

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