Tag Archives: DiaBeta

Metformin Hydrochloride

  By admin | June 20, 2010 - 6:49 am | Diabetes drugs
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Drug Approvals (British Approved Name Modified, US Adopted Name, rINN) International Nonproprietary Names (INNs) in main languages (French, Latin, and Spanish): Hidrocloruro de metformina; LA-6023 (metformin or metformin hydrochloride); Metformiinihydrokloridi; Metformin Hidroklorur; Metformin hydrochlorid; Metformine, chlorhydrate de; Metformin-hidroklorid; Metforminhydroklorid; Metformini hydrochloridum; Metformino hidrochloridas. C4H11N5,HCI = 165,6. CAS — 657-24-9 (metformin); 1115-70-4 (metformin hydrochloride). ATC — A10BA02. Pharmacopoeias. In China, Europe, Japan, and US. European Pharmacopoeia, 6th ed. (Metformin Hydrochlonde). White or almost white crystals. Freely soluble in water slightly soluble in alcohol practically insoluble in acetone and in dichloromethane. The United States Pharmacopeia 31, 2008 (Metformin Hydrochloride). A white crystalline powder. Freely soluble in … Continue reading →

Glibenclamide

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  By admin | June 17, 2010 - 6:26 am | Diabetes drugs
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Drug Approvals (British Approved Name, rINN) International Nonproprietary Names (INNs) in main languages (French, Latin, and Spanish): Glibenclamida; Glibenclamidum; Glibenklamid; Glibenklamidas; Glibenklamidi; Glybenclamide; Glybenzcyclamide; Glyburide (US-AN); HB-419; U-26452 C23H28CIN305S = 494.0. CAS — 10238-21-8. ATC — A10BB01. Note. The name glibornuride has frequently but erroneously been applied to glibenclamide. Pharmacopoeias. In China, Europe, International, Japan, and US. European Pharmacopoeia, 6th ed. (Glibenclamide). A white or almost white, crystalline powder. Practically insoluble in water slightly soluble in alcohol and in methyl alcohol sparingly soluble in dichloromethane. The United States Pharmacopeia 31, 2008 (Glyburide). Store in airtight containers. Adverse Effects, Treatment, and Precautions As for … Continue reading →

Current Oral Antidiabetic Therapy: Sulfonylureas

  By admin | March 5, 2010 - 6:57 am | Drugs
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These agents are derivatives of sulfonic acid and urea, and produce their effects by binding to receptors on the surface of pancreatic beta cells. The binding of sulfonylureas results in depolarization of the cell membrane, the influx of calcium ions, and subsequent release of insulin. The sulfonylureas were developed in 1954 and continue to be the most widely prescribed oral agents for the treatment of type 2 diabetes. Early evidence of associated increased cardiovascular morbidity has not been reproduced, and today sulfonylureas are considered relatively safe agents that have proven effective over long-term use. Sulfonylureas: First-Generation Sulfonylureas consists of two groups or generations of agents. The first-generation agents are … Continue reading →

Type 2 Diabetes: Antidiabetic Agents

  By admin | December 26, 2009 - 6:18 am | Type 2 diabetes
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All patients with type 1 diabetes are dependent on exogenous insulin administration, whereas patients with type 2 diabetes have a relative, not an absolute, insulin deficiency. If monitoring and lifestyle changes alone do not produce adequate glucose control of type 2 diabetes, oral antidiabetic agents will be prescribed. Diet, exercise, and optimal use of oral antidiabetic agents (alone or in combination) may be enough to counteract insulin resistance and thus achieve effective glycemic control. However, due to progressive pancreatic b-cell deterioration, many patients with type 2 diabetes eventually become unable to produce sufficient insulin. In such cases daily insulin self-injections will be needed. Oral antidiabetic drugs fall … Continue reading →