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        | What other disease besides DM can metformin be used for |  | Definition 
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        | glimepiride/rosiglitazone |  | 
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        | What is sulfonylureas main MOA |  | Definition 
 
        | binds to beta cells and increases secretion of insulin (also has minimal effect on decreasing hepatic gluconeogenesis and increasing insulin sensitivity)
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        | Pts with liver disease are at risk for hypoglycemia while on which sulfonylureas |  | Definition 
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        | Pts which renal insufficiencies (CrCl <50) are at risk for hypoglycemia while on which sulfonylureas |  | Definition 
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        | When should sulfonylureas be taken |  | Definition 
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        | What would be the ideal pt for a sulfonylurea |  | Definition 
 
        | A1c <9% and NOT morbidly obese |  | 
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        | What is the MOA of the meglitinides |  | Definition 
 
        | Closes ATP-sensitive K+ channels on beta cells and increases insulin secretion |  | 
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        | decreases hepatic gluconeogenesis (also increases insulin sensitivity, and decreases GI glucose absorption)
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        | which diabetic agent should be held for imaging studies with contrast dye |  | Definition 
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        | at what SCr levels should metformin be stopped |  | Definition 
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        | which diabetic medication has been shown to reduce macrovascular complications in obese pts |  | Definition 
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        | which diabetic medication is good for pts with central obesity |  | Definition 
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        | what is the MOA of alpha-glucosidase inhibitors |  | Definition 
 
        | prevents the breakdown of complex sugars to glucose |  | 
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        | if a pt on an alpha-glucosidase inhibitor has a hypoglycemic even, how would they treat it |  | Definition 
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        | activates PPAR receptor increasing insulin sensitivity (also decreases hepatic gluconeogenesis)
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        | TZDs are contraindicated in which pts |  | Definition 
 
        | NYHA class III-IV HF liver enzymes 2.5x ULN
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        | what is the MOA of pramlintide |  | Definition 
 
        | mimics exogenous amylin's effects and slows gastric emptying, suppression of glucagon secretion, and promotion of satiety |  | 
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        | how would you adjust a pts insulin dose when starting Symlin |  | Definition 
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        | how do incretin memetics work |  | Definition 
 
        | Binds to and activates GLP1 receptors resulting in enhanced glucose-dependent insulin secretion, slowed gastric emptying, suppression of glucagon secretion, and promotion of satiety |  | 
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        | which diabetic drug class can cause acute pancreatitis |  | Definition 
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        | which diabetic drug can cause thyroid cancer |  | Definition 
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        | which two diabetic drug classes can cause weight LOSS |  | Definition 
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        | what is the MOA of Januvia |  | Definition 
 
        | inhibits DPP-IV preventing the breakdown of endogenous incretins like GLP-1 |  | 
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        | which diabetic drug can cause Steve-Johnson's syndrome |  | Definition 
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        | Which of the following oral diabetic agents is most effective at lowering the A1c? 
 A. Glimepiride
 B. Acarbose
 C. Sitagliptin
 D. They all lower the A1c equally well
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        | what is the only cloudy insulin |  | Definition 
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        | Which insulin is available without a prescription |  | Definition 
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        | what are the rapid acting insulins |  | Definition 
 
        | lispro (Humalog), aspart (Novolog), glulisine (Apidra) |  | 
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        | what is the initial dosing for insulin |  | Definition 
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        | what is the 2/3, 1/3 rule with insuline |  | Definition 
 
        | give 2/3 of the daily dose of insulin in the AM and give 1/3 in the PM |  | 
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        | once opened, how long are insulin vials good for |  | Definition 
 
        | 28 days (execption detemir- 42 days)
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        | which insulins should not be mixed with others |  | Definition 
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