If the drug is discontinued, and if diet alone is inadequate for controlling blood glucose, insulin therapy should be considered.Safety and effectiveness in pediatric patients have not been established.Elderly patients are particularly susceptible to the hypoglycemic action of glucose lowering drugs. If the insulin dose is more than 40 units daily, a transition period is required for conversion to Micronase. USPI Micronase ; See related articles. When transferring patients from oral hypoglycemic agents other than chlorpropamide to Micronase, no transition period and no initial or priming dose are necessary. Use of Micronase or other antidiabetic medications must be viewed by both the physician and patient as a treatment in addition to diet and not as a substitution or as a convenient mechanism for avoiding dietary restraint. If hypoglycemic coma is diagnosed or suspected, the patient should be given a rapid intravenous injection of concentrated (50%) glucose solution. Because Micronase b belongs to the class of sulfonylurea agents, caution should be used in patients with G6PD deficiency and a non-sulfonylurea alternative should be considered.

Hypoglycemia is more likely to occur when caloric intake is deficient, after severe or prolonged exercise, when alcohol is ingested, or when more than one glucose lowering drug is used. In some cases these were transient and disappeared despite continue therapy. These may be transient and may disappear despite continued therapy. "Product Information. The risk of hypoglycemia may be increased with combination therapy.When a patient stabilized on any diabetic regimen is exposed to stress such as fever, trauma, infection or surgery, a loss of control may occur. Cerner Multum, Inc. "UK Summary of Product Characteristics." You may report them to the The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. If the insulin dose is between 20 and 40 units daily, the patient may be placed directly on Micronase Tablets 5 mg daily as a single dose.

A second metabolite, the 3-cishydroxy derivative, also occurs. Primary and secondary failure also should be explained.In initiating treatment for type 2 diabetes, diet should be emphasized as the primary form of treatment. Patient Savings Offers. Dose selection should include assessment of renal function.Cholestatic jaundice and hepatitis may occur rarely which may progress to liver failure; Micronase Tablets should be discontinued if this occurs.Liver function abnormalities, including isolated transaminase elevations, have been reported.Porphyria cutanea tarda and photosensitivity reactions have been reported with sulfonylureas.Leukopenia, agranulocytosis, thrombocytopenia, hemolytic anemia (see Hepatic porphyria and disulfiram-like reactions have been reported with sulfonylureas; however, hepatic porphyria has not been reported with Micronase and disulfiram-like reactions have been reported very rarely.Cases of hyponatremia have been reported with glyburide and all other sulfonylureas, most often in patients who are on other medications or have medical conditions known to cause hyponatremia or increase release of antidiuretic hormone. Some of the dosage forms listed on this page may not apply to the brand name Micronase.. For the Consumer. Inactive ingredients: colloidal silicon dioxide, dibasic calcium phosphate, magnesium stearate, microcrystalline cellulose, sodium alginate, talc. If generic versions of this product have been approved by the FDA, there may be Micronase Tablets contain glyburide, which is an oral blood-glucose-lowering drug of the sulfonylurea class. With concomitant glyburide and metformin therapy, the risk of hypoglycemia associated with sulfonylurea therapy continues and may be increased. Available for Android and iOS devices. Glyburide is a white, crystalline compound, formulated as Micronase Tablets of 1.25, 2.5, and 5 mg strengths for oral administration.

Bullous reactions, erythema multiforme, and exfoliative dermatitis have been reported. Doctors give unbiased, trusted information on whether Glyburide can cause or treat Allergies: Dr. Anand on micronase allergy signs: Allergic too it.See drug insert. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.Some side effects may not be reported. Progressive withdrawal of insulin and increase of Micronase in increments of 1.25 to 2.5 mg every 2 to 10 days is then carried out. Micronase (glyburide)." Mild hypoglycemic symptoms, without loss of consciousness or neurological findings, should be treated aggressively with oral glucose and adjustments in drug dosage and/or meal patterns. Displacement from protein binding sites by other drugs may lead to enhanced hypoglycemic action. Side effects requiring immediate medical attention.

However, attempts should be made to identify the optimal dose of each drug needed to achieve this goal. Caloric restriction and weight loss are essential in the obese diabetic patient. When such drugs are withdrawn from a patient receiving Micronase, the patient should be observed closely for hypoglycemia.A possible interaction between glyburide and ciprofloxacin, a fluoroquinolone antibiotic, has been reported, resulting in a potentiation of the hypoglycemic action of glyburide.

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