Nateglinide

Table of contents

  • Brand Names
  • Chemistry
  • Pharmacologic Category
  • Mechanism of Action
  • Therapeutic Use
  • Pregnancy and Lactation Implications
  • Contraindications
  • Warnings and Precautions
  • Adverse Reactions
  • Caution and personalized dose adjustment in patients with the following genotypes
  • Other genes that may be involved
  • Substrate of
  • Inhibits
  • Drug Interactions
  • Nutrition/Nutraceutical Interactions
  • Dosage
  • Pharmacokinetics and Pharmacodynamics
  • Special Considerations

Brand Names

Europe

Austria: Starlix; Bulgaria: Starlix; Cyprus: Starlix; Czech Republic: Starlix; Estonia: Starlix; Finland: Starlix; France: Starlix; Germany: Starlix; Greece: Starlix; Hungary: Starlix; Ireland: Starlix; Italy: Starlix; Latvia: Starlix; Lithuania: Starlix; Luxembourg: Starlix; Malta: Starlix; Netherlands: Starlix; Poland: Starlix; Portugal: Starlix; Romania: Starlix; Slovakia: Starlix; Slovenia: Starlix; Spain: Starlix; Sweden: Starlix; UK: Starlix.

North America

Canada: Starlix; USA: Starlix.

Latin America

Argentina: Starlix; Brazil: Starlix; Mexico: Starlix.

Asia

Japan: Fastic, Starsis.

Drug combinations

Chemistry

Nateglinide: C~19~H~27~NO~3~. Mw: 317.42. (1) D-Phenylalanine, N-[[trans-4-(1-methylethyl)cyclohexyl]carbonyl]-; (2)(-)-N-[(trans-4-Isopropylcyclohexyl)carbonyl-D-phenylalanine. CAS-105816-04-4 (2000).

Pharmacologic Category

Antidiabetic Agents; Meglitinides. (ATC-Code: A10BX03).

Mechanism of action

Stimulates insulin release from pancreatic β-cells to reduce postprandial hyperglycemia.

Therapeutic use

Management of type 2 diabetes mellitus (non-insulin-dependent) as monotherapy. In combination with metformin or a thiazolidinedione to lower blood glucose in hyperglycemia.

Pregnancy and lactiation implications

Should not be used during pregnancy. Abnormal blood glucose levels associated with higher incidence of congenital abnormalities. Insulin is drug of choice for control of diabetes mellitus during pregnancy. Not recommended in nursing women.

Unlabeled use

Contraindications

Hypersensitivity to nateglinide or any component of the formulation. Diabetic ketoacidosis, with or without coma. Type 1 diabetes mellitus (insulin-dependent).

Warnings and precautions

May cause hypoglycemia. Use with caution in adrenal and/or pituitary impairment (may be more susceptible to glucose-lowering effects), in moderate-to-severe hepatic impairment, and in severe renal impairment (may be more susceptible to glucose-lowering effects). It may be necessary to discontinue nateglinide and administer insulin if patient exposed to stress (i.e. fever, trauma, infection, surgery). Patients not adequately controlled on oral agents which stimulate insulin release (e.g. glyburide) should not be switched to nateglinide or have nateglinide added to therapy. Indicated for adjunctive therapy with metformin (not to be used as substitute for metformin monotherapy). Combination treatment with sulfonylureas not recommended (no additional benefit). Use with caution in the elderly and in malnourished patients (may be more susceptible to glucose-lowering effects).

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