Initial U.S. Approval: 2005
BYETTA is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
Facts about exenatide Injection
Approval Date: 2005
Proprietary Name: BYETTA (exenatide) Injection
Active Ingredient(s): exenatide
FDA-approved use: 2 diabetes mellitus.
Dosage Form: BYETTA is supplied as 250 mcg/mL exenatide in: • 5 mcg per dose, 60 doses, 1.2 mL prefilled pen • 10 mcg per dose, 60 doses, 2.4 mL prefilled pen.
Medicine Approved By: Food and Drug Administration (FDA)
Manufacturer: Amylin Pharmaceuticals, Inc.
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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Query For exenatide Injection
Exenatide is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type Exenatide, is a medication used to treat diabetes mellitus type 2. Note: (see Drugs@FDA for complete indication)
What is BYETTA? • BYETTA is an injectable prescription medicine that may improve blood sugar (glucose) control in adults with type 2 diabetes mellitus, when used with a diet and exercise program. • BYETTA is not insulin. • You should not take BYETTA instead of insulin. • The use of BYETTA with insulin is not recommended. • BYETTA is not for people with type 1 diabetes or people with diabetic ketoacidosis. • It is not known if BYETTA is safe and effective in children. • BYETTA has not been studied in people who have pancreatitis. • BYETTA should not be used in people who have severe kidney problems. Active Ingredient: exenatide Inactive Ingredients: metacresol, mannitol, glacial acetic acid, and sodium acetate trihydrate in water for injection.
How To access exenatide Injection?
BYETTA (exenatide) Injection Initial U.S. Approval: 2005
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