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balsalazide disodium |
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balsalazide disodium Colazide (UK), Colazal Pharmacologic class: GI agent Therapeutic class: Anti-inflammatory Pregnancy risk category B ActionMetabolized in colon to mesalamine and then to 5-aminosalicylclic acid, both of which are thought to exert local anti-inflammatory effect by inhibiting prostaglandin and acid metabolites AvailabilityCapsules: 750 mg ⊘Indications and dosages ➣ Mildly to moderately active ulcerative colitis Adults: Usual dosage, three 750-mg capsules P.O. t.i.d. (6.75 g daily) for up to 8 weeks; some patients may require 12 weeks Children ages 5 to 17: Usual dosage, either three 750-mg capsules P.O. t.i.d (6.75 g daily) for up to 8 weeks, or one 750-mg capsule P.O. t.i.d. (2.25 g daily) for up to 8 weeks. Contraindications• Hypersensitivity to balsalazide, salicylates, or mesalamine PrecautionsUse cautiously in: Administration• Advise patient to swallow capsules whole, either always with or always without food.
Adverse reactionsCNS: headache, insomnia, dizziness, anxiety, confusion, agitation, coma EENT: blurred vision, eye irritation, tinnitus, earache, epistaxis, sinusitis, sore throat, nasopharyngitis GI: nausea, vomiting, diarrhea, constipation, abdominal pain, dyspepsia, anorexia, oral blisters, oral candidiasis, GI hemorrhage GU: urinary tract infection Musculoskeletal: arthralgia; myalgia; bone, back, neck, or limb pain Respiratory: cough, upper respiratory tract infection Skin: erythema Other: generalized pain InteractionsDrug-drug. Oral antibiotics: interference with balsalazide action Patient monitoring• Assess character and frequency of stools. Patient teaching• Instruct patient to take drug only as directed. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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| Salix submitted an NDA seeking approval to market an 1100 mg tablet formulation of balsalazide disodium (balsalazide tablet) for the treatment of mildly to moderately active ulcerative colitis to the FDA on July 17, 2007. Most notably, on July 17 the FDA received our New Drug Application seeking approval to market an 1100 mg tablet formulation of balsalazide disodium. Food and Drug Administration (FDA) a New Drug Application (NDA) seeking approval to market a 1100 milligram tablet formulation of balsalazide disodium (balsalazide tablet). |
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