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Amaryl - Glimepiride

Amaryl (Glimepiride) 6.9 (0.3) 7.2 (0.3) 5.8 (0.2) A second-generation sulfonylurea. Blocks ATP-sensitive K-channels in the membrane of beta cells, stimulating the release of insuhn. [Pg.61]

Exenatide (Byetta) Glimepiride (Amaryl) Glimepiride/Pioglitazone (Duetact)... [Pg.44]

Glimepiride (Y) Amaryl Short-acting insulin secretagogues 1,2,4 1-2 0.5-1 2 8 24 hours Metabolized in liver to inactive metabolites... [Pg.229]

Glimepiride (Amaryl) is metabolized to at least one active metabolite. It is quickly absorbed from the gastrointestinal tract within an hour of oral administration and excreted in the urine and feces. Its half-life varies from 5 to 9 hours depending on the frequency of multiple dosing. [Pg.773]

The sulfonylureas stimulate insulin secretion by pancreatic cells. As an old class of diabetes drug, the sulfonylureas have been improved steadily over the years. The original sulfonylurea is tolbutamide (A.66) (Figure A.21). Later and more potent sulfonylureas include glipizide (Glucotrol, A.67), glyburide (A.68), and finally glimepiride (Amaryl, A.69). [Pg.368]

Second Generation o Glimepiride Amaryl o Glipizide Glucotrol... [Pg.6]

See other pages where Amaryl - Glimepiride is mentioned: [Pg.351]    [Pg.45]    [Pg.526]    [Pg.634]    [Pg.44]    [Pg.351]    [Pg.45]    [Pg.526]    [Pg.634]    [Pg.44]    [Pg.500]    [Pg.502]    [Pg.654]    [Pg.178]    [Pg.119]    [Pg.949]    [Pg.178]    [Pg.487]    [Pg.1011]    [Pg.415]    [Pg.958]    [Pg.1373]    [Pg.339]    [Pg.340]    [Pg.655]    [Pg.13]    [Pg.301]    [Pg.500]    [Pg.502]    [Pg.178]    [Pg.1288]    [Pg.196]   


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Amaryl

Glimepiride

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