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Valley Medical Pharmacy
630 Main Street (Store open 8.30to 5.30pm)
Brawley, CA 92227 eRx ID#0585957

1-800-322-0808/760-344-6303/FAX-760-344-6321 Toll Free Fax#855-322-0808 Store Op
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Prescription Drugs-C > Carafate > Carafate 1gm/10ml Suspension 1X414 ml Mfg.by: Axcan Pharma Us Inc USA

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Carafate 1gm/10ml Suspension 1X414 ml Mfg.by: Axcan Pharma Us Inc USA

This item requires a valid order from a physician licensed in the USA. Item No.: RXD3590288/RXB10025151 NDC No.: 58914-0170-14 Compare to: UPC No.: 358914170143 Mfg.Item No.:017014

$ 120.34         

Please Provide Us The Name, Address, Phone #, Fax #, State Lic.#, Name Of State, Dea#, And Npi# Of Ordering Physician. Please Provide All Information Available And Ask Your Physician To Fax Us The Prescription At 760-344-6321 For The Quantity.

Quantity:    

DESCRIPTION CARAFATE Tablets contain sucralfate and sucralfate is an a-D-glucopyranoside, β-D-fructofuranosyl-, octakis-(hydrogen sulfate), aluminum complex.

Click Here for Prescribing Information

INDICATIONS CARAFATE® (sucralfate) is indicated in: * Short-term treatment (up to 8 weeks) of active duodenal ulcer. While healing with sucralfate may occur during the first week or two, treatment should be continued for 4 to 8 weeks unless healing has been demonstrated by x-ray or endoscopic examination. * Maintenance therapy for duodenal ulcer patients at reduced dosage after healing of acute ulcers. DOSAGE AND ADMINISTRATION Active Duodenal Ulcer. The recommended adult oral dosage for duodenal ulcer is 1 g four times per day on an empty stomach. Antacids may be prescribed as needed for relief of pain but should not be taken within one-half hour before or after sucralfate. While healing with sucralfate may occur during the first week or two, treatment should be continued for 4 to 8 weeks unless healing has been demonstrated by x-ray or endoscopic examination. Maintenance Therapy: The recommended adult oral dosage is 1 g twice a day. Elderly: In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. (See PRECAUTIONS Geriatric Use) SIDE EFFECTS Adverse reactions to sucralfate in clinical trials were minor and only rarely led to discontinuation of the drug. In studies involving over 2700 patients treated with sucralfate tablets, adverse effects were reported in 129 (4.7%). Constipation was the most frequent complaint (2%). Other adverse effects reported in less than 0.5% of the patients are listed below by body system: Gastrointestinal: diarrhea, nausea, vomiting, gastric discomfort, indigestion, flatulence, dry mouth Dermatological: pruritus, rash Nervous System: dizziness, insomnia, sleepiness, vertigo Other: back pain, headache Postmarketing reports of hypersensitivity reactions, including urticaria (hives), angioedema, respiratory difficulty, rhinitis, laryngospasm, and facial swelling have been reported in patients receiving sucralfate tablets. Similar events were reported with sucralfate suspension. However, a causal relationship has not been established. Bezoars have been reported in patients treated with sucralfate. The majority of patients had underlying medical conditions that may predispose to bezoar formation (such as delayed gastric emptying) or were receiving concomitant enteral tube feedings. Inadvertent injection of insoluble sucralfate and its insoluble excipients has led to fatal complications, including pulmonary and cerebral emboli. Sucralfate is not intended for intravenous administration.

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