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Generic Diamox Acetazolamide 250mg

Your doctor will not prescribe this medication for you if your sodium or potassium levels are low, or if you have kidney or liver disease, including cirrhosis. Diamox may appear in breast milk and could affect a nursing infant. Glaucoma This medication is used as an addition to regular glaucoma treatment. Dosages for open-angle glaucoma range from 250 milligrams to 1 gram per 24 hours in 2 or more smaller doses. Your doctor will supervise your dosage and watch the effect of this medication carefully if you are using it for glaucoma. In secondary glaucoma and before surgery in acute congestive (closed-angle) glaucoma, the usual dosage is 250 milligrams every 4 hours or, in some cases, 250 milligrams twice a day. Some people may take 500 milligrams to start, and then 125 or 250 milligrams every 4 hours.

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Why Should Diamox Not Be Prescribed?

Increasing the dose does not increase the diuresis and may increase the incidence of drowsiness and/or paresthesia. The effects of Diamox during pregnancy have not been adequately studied. If you are pregnant or plan to become pregnant, inform your doctor immediately. The injectable form of this drug is occasionally used in acute cases. In a bacterial mutagenicity assay, Diamox was not mutagenic when evaluated with and without metabolic activation. There are no adequate and well-controlled studies in pregnant women. No specific antidote is known. Treatment should be symptomatic and supportive. Electrolyte imbalance, development of an acidotic state, and central nervous system effects might be expected to occur. Serum electrolyte levels (particularly potassium) and blood pH levels should be monitored.

Important Safety Information:

Symptoms of over dosage of Diamox are made evident by the following: Drowsiness , Decreased appetite , Nausea , Vomiting , Dizziness , Dumbness or tingling , Shaking , Ringing in the ears . To monitor for hematologic reactions common to all sulfonamides, it is recommended that a baseline CBC and platelet count be obtained on patients prior to initiating Diamox therapy and at regular intervals during therapy. If significant changes occur, early discontinuance and institution of appropriate therapy are important.