Antidiabetic Agents CHAPTER BIGUANIDES

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ajt/shutterstock, Inc. CHAPTER 2 Antidiabetic Agents Charles Ruchalski, PharmD, BCPS BIGUANIDES For newly diagnosed patients with type 2 diabetes, the biguanide metformin is the drug of choice for initial therapy, adjunctive to diet and exercise. It is often used in combination with other oral antidiabetic agents and/or insulin in patients who do not reach glycemic goals on those therapies. HbA1c reductions with metformin are generally between 1.5% and 2%. Metformin is contraindicated in certain patients to prevent lactic acidosis, a rare but serious side effect (approximately 0.03 cases per 1000 patient-years, with approximately 0.015 fatal cases per 1000 patient-years). Biguanides improve glucose tolerance by lowering both basal and postprandial plasma glucose. They decrease hepatic glucose production and intestinal absorption of glucose and improve insulin sensitivity by increasing peripheral glucose uptake and utilization through the activation of adenosine monophosphate-activated protein kinase (AMPK). Metformin Fortamet, Glucophage, Glucophage XR, Glumetza, Riomet, D-Care DM2 s Metformin, metformin extended-release, extended-release tablet, oral solution Usage Type 2 diabetes mellitus, prevention of type 2 diabetes mellitus, gestational diabetes, polycystic ovary syndrome, antipsychotic-induced weight gain Initial dose: 500 mg twice daily with morning and evening meals, 850 mg once daily with a meal, or 500 mg extended-release once daily with a meal Maintenance dose: 2000 2550 mg daily in divided doses or 2000 mg extended-release once daily (2500 mg daily with Fortamet) Renal dosage adjustment: GFR: > 45 ml/min: no dosage adjustment necessary, GFR: 30 45 ml/min: 50% dose reduction, GFR < 30 ml/min, Use is contraindicated Adverse Reactions: Most Common Diarrhea, vomiting, dyspepsia, flatulence, metallic taste, weight loss Adverse Reactions: Rare/Severe/Important Lactic acidosis, megaloblastic anemia Major Drug Interactions Drugs Affecting Metformin Alcohol potentiates the effect on lactate metabolism Cimetidine increases plasma concentrations (use alternative H2 blocker) Iodinated contrast media can lead to acute renal failure and metformin toxicity Contraindications GFR < 30 ml/min, acute or chronic metabolic acidosis Essential Monitoring Parameters HbA1c at least twice a year, serum glucose, renal function Counseling Point Discontinue immediately and promptly notify healthcare practitioner if unexplained myalgia, malaise, hyperventilation, or unusual somnolence occur because those are symptoms of lactic acidosis 29

Key Points Black Box Warnings: Lactic acidosis. (This rare but serious metabolic complication can occur; when it occurs, it is fatal 50% of the time) Temporarily withhold in patients undergoing radiologic procedures involving the parenteral administration of iodinated contrast media because it may result in acute alteration of renal function. Do not restart for at least 48 hours or until renal function appears adequate. DI-PEPTIDYL PEPTIDASE-4 INHIBITORS Di-peptidyl peptidase-4 (DPP-4) inhibitors inhibit the breakdown of active Glucagon-Like Peptide-1 (GLP-1) to inactive GLP-1 through the inhibition of the DPP-4 enzyme. Active GLP-1 is released from the alpha cells of the pancreas in response to food intake. GLP-1 plays a role in regulating blood glucose by increasing the secretion of insulin from the pancreas in a glucose-dependent manner. GLP-1 also helps regulate glucagon secretion and decreases hepatic glucose production. Those drugs are used as monotherapy as an adjunct to diet and exercise or in combination with other oral antidiabetic agents in patients who do not reach glycemic goals. Average HbA1c reductions are between 0.7% and 1%. Inhibition of DPP-4 enhances the activity of active GLP-1, thus increasing glucose-dependent insulin secretion and decreasing levels of circulating glucagon and hepatic glucose production Members of the Drug Class In this section: Sitagliptin Others: Alogliptin, linagliptin, saxagliptin Sitagliptin Januvia Sitagliptin Usage Type 2 diabetes mellitus 100 mg once daily with or without food Renal dosage adjustment: 50 mg once daily: GFR 30 to < 50 ml/min 25 mg once daily: GFR < 30 ml/min Adverse Reactions: Most Common Nasopharyngitis, nausea, diarrhea, vomiting, hypoglycemia, weight loss Adverse Reactions: Rare/Severe/Important Acute pancreatitis, arthralgia, bullous pemphigoid, rash (Stevens-Johnson syndrome) Major Drug Interactions Sitagliptin s Effect on Other Drugs Digoxin: Increased levels Contraindications Severe hypersensitivity reactions Essential Monitoring Parameters HbA1c at least twice a year, serum glucose, renal function Counseling Point Discontinue immediately and promptly notify healthcare practitioner if unexplained persistent nausea and vomiting occur (signs of acute pancreatitis) 30 CHAPTER 2 Antidiabetic Agents

GLUCAGON-LIKE PEPTIDE-1 AGONIST Active Glucagon-Like Peptide-1 (GLP-1) is released from the alpha cells of the pancreas in response to food intake. GLP-1 plays a role in regulating blood glucose by increasing the secretion of insulin from the pancreas in a glucose-dependent manner. GLP-1 also helps regulate glucagon secretion and decreases hepatic glucose production. These drugs are used as monotherapy as an adjunct to diet and exercise or in combination with other oral antidiabetic agents in patients who do not reach glycemic goals. Average HbA1c reductions are between 0.5% and 1% with immediate release and 1.5% to 2% with extended release. Glucagon-Like Peptide-1 (GLP-1) agonist enhances glucosedependent insulin secretion and decreases levels of circulating glucagon and hepatic glucose production Usage Type 2 diabetes mellitus Adverse Reactions for the Drug Class: Most Common Hypoglycemia (when used with other oral antidiabetic drugs that may cause hypoglycemia), nausea, diarrhea, vomiting, hyperhidrosis, constipation, injection-site reactions Adverse Reactions for the Drug Class: Rare/Severe/Important Increased incidence of Thyroid C-Cell tumors, acute pancreatitis, acute renal failure Major Drug Interactions for the Drug Class Glucagon-Like Peptide-1 (GLP-1) Effects on Other Drugs Oral contraceptives: Decreased efficacy Warfarin: Enhanced efficacy Contraindications for the Drug Class Family history of medullary thyroid carcinoma or patients with multiple endocrine neoplasia syndrome Essential Monitoring Parameters HbA1c at least twice a year, serum glucose, renal function, GI distress, injection-site reactions Key Point Black Box Warning: Dose-dependent and treatment-duration- dependent Thyroid C-cell tumors, including medullary thyroid carcinoma Counseling Point for the Drug Class Discontinue immediately and promptly notify healthcare practitioner if unexplained persistent nausea and vomiting occur (signs of acute pancreatitis) Members of the Drug Class In this section: Exenatide and liraglutide Others: Albiglutide, dulaglutide, and lixisenatide Exenatide Byetta, Bydureon s Exenatide and Exenatide ER Sub-Q injection Initial dose: Immediate-release: (Byetta) 5 µg twice daily within 60 minutes prior to a meal, extendedrelease: (Bydureon) 2 mg once weekly Maintenance dose: Immediate-release: (Byetta) 10 µg twice daily; extended-release: (Bydureon) 2 mg once weekly Renal dosage adjustment: GFR < 30 ml/min, Use is contraindicated Liraglutide Victoza, Saxenda Liraglutide Sub-Q injection Usage Type 2 diabetes mellitus (Victoza), weight loss as an adjunct to diet and exercise (Saxenda) Initial dose: 0.6 mg once daily for 1 week, then 1.2 mg once weekly Maintenance dose: 1.2 mg to 1.8 mg once weekly Renal dosage adjustment: No dosage adjustment necessary 2 Antidiabetic Agents Glucagon-Like Peptide-1 Agonist 31

INSULIN The hormone insulin is endogenously released from the beta cells of the pancreas. Patients with type 1 diabetes mellitus have an absolute deficiency of insulin; patients with type 2 diabetes mellitus may also have decreased production of endogenous insulin. Type 1 diabetics require insulin as a lifelong treatment. Insulin is commonly used in type 2 diabetic patients as either adjunct therapy to oral antidiabetic agents or as monotherapy as the disease progresses. Various substitutions on the insulin molecule and other modifications have led to multiple types of insulin. They are characterized and administered based on their pharmacodynamic and pharmacokinetic characteristics, such as onset, peak, and duration of action. The various types of insulin are classified as rapid-acting, short-acting, intermediate-acting, or long-acting insulin. Insulin lowers blood glucose by stimulating peripheral glucose uptake, especially in skeletal muscle and fat, and by inhibiting hepatic glucose production Usage for the Drug Class Type 1 diabetes mellitus, type 2 diabetes mellitus, hyperkalemia, diabetic ketoacidosis/diabetic coma for the Drug Class Initial dose: 0.5 1 unit/kg per day SUB-Q (high interpatient variability) Maintenance dose: Adjust doses to achieve premeal blood glucose levels of 80 130 mg/dl Renal dosage adjustment: GFR 10 50 ml/min: Administer 75% of normal dose GFR < 10 ml/min: Administer 25 50% of normal dose; monitor closely Adverse Reactions for the Drug Class: Most Common Hypoglycemia (anxiety, blurred vision, palpitations, shakiness, slurred speech, sweating), weight gain Adverse Reactions for the Drug Class: Rare/Severe/Important Severe hypoglycemia (seizure/coma), edema, lipoatrophy or lipohypertrophy at injection site Major Drug Interactions for the Drug Class Drugs Affecting Insulin (Decreased Hypoglycemic Effect) Acetazolamide Diuretics Oral contraceptives Albuterol Epinephrine Phenothiazines Asparaginase Estrogens Terbutaline Corticosteroids HIV antivirals Thyroid hormones Diltiazem Lithium Drugs Affecting Insulin (Increased Hypoglycemic Effect) Alcohol Fluoxetine Anabolic steroids Lithium Beta blockers Sulfonamides Clonidine Contraindications for the Drug Class Severe hypoglycemia; allergy or sensitivity to any ingredient of the product Essential Monitoring Parameters for the Drug Class HbA1c at least twice a year, serum glucose, renal function, injection-site reactions Counseling Points for the Drug Class Follow a prescribed diet and exercise regularly Rotate injection sites to prevent lipodystrophy Insulin requirements may change during times of illness, vomiting, fever, and emotional stress Wear diabetic identification Insulin stored at room temperature will be less painful to inject compared with refrigerator-stored insulin Mild episodes of hypoglycemia may be treated with oral glucose or carbohydrates Members of the Drug Class In this section: Insulin inhalation powder, insulin glulisine, insulin lispro, insulin NPH, insulin (R), insulin glargine, insulin detemir, insulin aspart, various mixtures are also available Insulin inhalation powder Afrezza Insulin inhalation powder Powder, inhalation (4-unit, 8-unit, and 12-unit cartridges) 32 CHAPTER 2 Antidiabetic Agents

Administer inhalation at the beginning of each meal. Start with four units for insulin-naïve patients. Adverse Reactions: Most Common Hypoglycemia, cough, throat irritation Contraindications Hypersensitivity to regular insulin, chronic lung disease (such as asthma or COPD) Key Points Black Box Warnings: Acute bronchospasm has been observed in patients with asthma and COPD. Contraindicated in patients with chronic lung disease (such as asthma or COPD). Before initiating, perform spirometry (FEV1) in all patients and assess every 6 months to 1 year. Avoid use in patients with active lung cancer. Insulin Glulisine Apidra, Apidra SoloSTAR Insulin glulisine (rapid-acting insulin) Administer SUB-Q 15 minutes before or immediately after starting a meal May be administered by continuous subcutaneous infusion (insulin pump) Insulin Lispro Humalog, Humalog KwikPen Insulin lispro (rapid-acting insulin) Injection 100 units/ml, 200 units/ml (10 ml vial and 3 ml cartridge for Administer SUB-Q 15 minutes before or immediately after starting a meal May be administered by continuous subcutaneous infusion (insulin pump) Insulin NPH Humulin N, Novolin N Insulin NPH (intermediate-acting insulin) OTC Injection, suspension, 100 units/ml (10 ml vial and 3 ml cartridge for NPH should only be mixed with regular insulin Draw regular insulin into the syringe first, then add the NPH insulin to the syringe Insulin Regular Humulin R, Novolin R Insulin regular (short-acting insulin) OTC Injection 500 units/ml (20 ml vial and 3 ml cartridge for (Humulin R) Administer SUB-Q 30 minutes before a meal May be administered by continuous subcutaneous infusion (insulin pump) Humulin R U-500 should be prescribed only for patients who require more than 200 units of insulin per day 2 Antidiabetic Agents Insulin 33

70% NPH and 30% Regular Insulin Mixture Humulin 70/30, Novolin 70/30 70% NPH and 30% regular insulin mixture OTC Injection, suspension, 100 units/ml (10 ml vial and 3 ml cartridge for 50% NPH and 50% Regular Insulin Mixture Humulin 50/50 50% NPH and 50% regular insulin mixture OTC Injection, suspension, 100 units/ml (10 ml vial and 3 ml cartridge for 75% Intermediate-Acting Lispro Suspension and 25% Rapid-Acting Lispro Solution Humalog Mix 75/25 75% intermediate-acting lispro suspension and 25% rapid-acting lispro solution Insulin Glargine Basaglar, Lantus, Lantus SoloSTAR, Toujeo SoloSTAR Insulin glargine Injection 300 units/ml (1.5 ml disposable pen) (Tuejo) When changing to insulin glargine from once-daily NPH, the initial dose of insulin glargine should be the same. When changing to insulin glargine from twicedaily NPH, the initial dose of insulin glargine should be reduced by 20% and adjusted according to patient response. Administer once daily Starting dose in a type 2 diabetic patient is 10 units at bedtime and then titrate according to patient response Insulin Detemir Levemir, Levemir FlexPen, Levemir FlexTouch Insulin detemir (long-acting insulin) Indicated for once-daily or twice-daily dosing Once daily is dosed with the evening meal or at bedtime Twice daily is dosed every 12 hours Insulin Aspart NovoLog, NovoLog FlexPen, NovoLog FlexTouch Insulin aspart (rapid-acting insulin) 34 CHAPTER 2 Antidiabetic Agents

Administer SUB-Q 15 minutes before or immediately after starting a meal May be administered by continuous subcutaneous infusion (insulin pump) 70% Intermediate-Acting Insulin Aspart Suspension and 30% Rapid-Acting Aspart Solution NovoLog Mix 70/30 70% Intermediate-Acting Insulin Aspart Suspension and 30% Rapid-Acting Aspart Solution Comparison of Insulin Products Refer to Table 2-1. 2 TABLE 2 1 Comparison of Insulin Products Product Onset (Hours) Peak (Hours) Duration (Hours) Appearance Rapid-Acting Insulin Insulin aspart (NovoLog) 0.25 1 2 3 5 Clear Insulin glulisine (Apidra) 0.25 1 3 4 Clear Insulin lispro (Humalog) 0.25 0.5 1.5 3 4 Clear Insulin Inhalation (Afrezza) 0.25 1 3 Powder Short-Acting Insulin Regular Insulin (Humulin R, Novolin R) 0.5 1 2 3 3 6 Clear Intermediate-Acting Insulin NPH insulin (Humulin N, Novolin N) 2 4 6 10 10 16 Cloudy Long-Acting Insulin Insulin detemir (Levemir) 4 N/A 12 24 Clear Insulin glargine (Basaglar, Lantus, Toujeo) 4 N/A 24 Clear Antidiabetic Agents SODIUM-GLUCOSE COTRANSPORTER 2 (SGLT-2) INHIBITORS The sodium-glucose cotransporter 2 (SGLT-2) inhibitors decrease plasma glucose by increasing urinary excretion of glucose. They are used as adjuncts to diet and exercise in patients with type 2 diabetes mellitus. Recent clinical data suggest that patients taking empagliflozin demonstrated a reduction in the risk of cardiovascular death. Average HbA1c reductions are between 0.7% and 1%. Sodium-glucose Cotransporter 2 (SGLT-2) inhibitors reduce reabsorption of filtered glucose from the proximal tubular lumen and decreases the renal threshold for glucose, thereby reducing plasma glucose concentrations Usage for the Drug Class Type 2 diabetes mellitus Adverse Reactions for the Drug Class: Most Common Hypoglycemia (when used with other oral antidiabetic drugs that may cause hypoglycemia), urinary tract infection, increased urine output, increased LDL cholesterol, nausea, genitourinary fungal infections Adverse Reactions for the Drug Class: Rare/Severe/Important Increased serum creatinine, hypotension, ketoacidosis, urosepsis Sodium-Glucose Cotransporter 2 (SGLT-2) Inhibitors 35

Major Drug Interactions for the Drug Class Drugs Affecting SGLT-2 Inhibitors Thiazides and Thiazide-like diuretics: Decreased efficacy SGLT-2 Inhibitors Effects on Other Drugs Loop diuretics: Increased risk for hypotension Contraindications for the Drug Class GFR < 30 ml/min, ESRD, hemodialysis Essential Monitoring Parameters for the Drug Class HbA1c at least twice a year, serum glucose, renal function Key Points Black Box Warnings: Increased risk of bone mineral loss and bone fractures Increased risk of acute kidney injury Members of the Drug Class In this section: Canagliflozin, Dapagliflozin, Empagliflozin Canagliflozin Invokana Canagliflozin Initial dose: 100 mg once daily prior to the first meal of the day Maximum recommended dose: 300 mg once daily in patients with GFR > 60 ml/min Renal dosage adjustment: GFR 45 ml/min to < 60 ml/min: Maximum 100 mg once daily GFR 30 ml/min to 45 ml/min: Not recommended for initiation of therapy GFR < 30 ml/min: Use is contraindicated Dapagliflozin Farxiga Dapagliflozin Initial dose: 5 mg once daily Maximum recommended dose: 10 mg once daily Renal dosage adjustment: GFR 30 60 ml/min: Drug is not recommended GFR < 30 ml/min: Use is contraindicated Empagliflozin Jardiance Empagliflozin Pregnancy Category: (Not recommended During Second or Third Trimester) Initial dose: 10 mg once daily Maximum recommended dose is 25 mg once daily Renal dosage adjustment: GFR 30 ml/min to 45 ml/min: Not recommended for initiation of therapy GFR < 30 ml/min: Use is contraindicated SULFONYLUREAS The sulfonylureas are used as adjunctive therapy to diet and exercise in patients with type 2 diabetes mellitus. Although periodically used as monotherapy, sulfonylureas are more commonly used in combination with other oral antidiabetic agents, sometimes in the same formulation, in patients who do not reach glycemic goals. General dosing guidelines are to start with a low dose and titrate upward according to patient response while monitoring for signs and symptoms of hypoglycemia, which is a common adverse effect 36 CHAPTER 2 Antidiabetic Agents

of the drug class. Those drugs should be used cautiously in patients with renal or hepatic impairment. Average HbA1c reductions are between 1% and 2%. Lowers blood glucose by stimulating insulin release from the beta cells of the pancreatic islets Usage for the Drug Class Type 2 diabetes mellitus for the Drug Class Exception: glyburide (pregnancy category B) Adverse Reactions for the Drug Class: Most Common Hypoglycemia, GI distress, dizziness Adverse Reactions for the Drug Class: Rare/Severe/Important SIADH (most commonly with chlorpropamide); disulfiramlike reactions Major Drug Interactions for the Drug Class Drugs Affecting Sulfonylureas Anticoagulants, azole antifungals, gemfibrozilenhanced hypoglycemic effects Beta blockers cause decreased hypoglycemic effects; also, may mask signs and symptoms of hypoglycemia Sulfonylureas Effects on Other Drugs Digoxin: Increased levels Contraindications for the Drug Class Diabetes complicated by ketoacidosis, with or without coma; Type 1 diabetes mellitus; diabetes complicated by pregnancy Essential Monitoring Parameters for the Drug Class HbA1c at least twice a year, serum glucose, renal function Counseling Point for the Drug Class Monitor glucose as directed and be aware of the signs and symptoms of hypoglycemia Members of the Drug Class In this section: Glimepiride, glipizide, glyburide Others: Chlorpropamide, tolazamide, tolbutamide Glimepiride Amaryl Glimepiride Initial dose: 1 2 mg once daily at breakfast Maintenance dose: 1 8 mg once daily Glipizide Glucotrol, Glucotrol XL s Glipizide, glipizide extended-release, extended-release tablet Initial dose: Glucotrol: 2.5 5 mg once daily 30 minutes before breakfast Glucotrol XL: 5 mg extended-release once daily with breakfast Maintenance dose: Glucotrol: 10 40 mg daily (> 15 mg/day should be divided) Glucotrol XL: 5 20 mg extended-release once daily Glyburide DiaBeta, Micronase, Glynase PresTab Glyburide DiaBeta and Micronase Initial dose: 1.25 5 mg once daily with breakfast Maintenance dose: 1.25 20 mg once daily; may give as single or divided doses Glynase PresTab Initial dose: 1.5 3 mg once daily with breakfast Maintenance dose: 1.5 12 mg once daily; may give as single or divided doses 2 Antidiabetic Agents Sulfonylureas 37

THIAZOLIDINEDIONES The thiazolidinediones decrease insulin resistance by enhancing insulin-receptor sensitivity. They are used as adjuncts to diet and exercise in patients with type 2 diabetes mellitus. Although periodically used as monotherapy, thiazolidinediones are more frequently used in combination with other oral antidiabetic agents in patients who do not reach glycemic goals. Clinical data suggest that patients taking thiazolidinediones may be at an increased risk of myocardial infarction and death; thus, they should be used with caution in patients with a history of previous cardiac disease. They are contraindicated in patients with NYHA class III or IV heart failure. A structurally similar thiazolidinedione, troglitazone, was removed from the market due to cases of liver failure and death. The current agents are recommended to avoid use in patients with hepatic dysfunction. Average HbA1c reductions are between 1% and 1.5%. Thiazolidinediones increase insulin sensitivity by affecting the peroxisome proliferator-activated receptor gamma (PPAR-γ). Acting as an agonist to this receptor, thiazolidinediones decrease insulin resistance in adipose tissue, skeletal muscle, and the liver. Usage for the Drug Class Type 2 diabetes mellitus Adverse Reactions for the Drug Class: Most Common Weight gain, edema, hypoglycemia (when used with other oral antidiabetic drugs that may cause hypoglycemia) Adverse Reactions for the Drug Class: Rare/Severe/Important Hepatic failure, heart failure, anemia, ovulation in anovulatory premenopausal women, bone loss, bladder cancer, macular edema Major Drug Interactions for the Drug Class Drugs Affecting Thiazolidinediones Gemfibrozil: Increased levels Rifampin: Decreased levels Thiazolidinediones Effects on Other Drugs Oral contraceptives: Decreased efficacy Contraindications for the Drug Class Patients with NYHA class III and IV heart failure; active liver disease (alanine aminotransferase [ALT] > 2.5 times the upper limit of normal) Essential Monitoring Parameters for the Drug Class HbA1c at least twice a year, serum glucose, liver function Key Points Black Box Warnings: Can exacerbate congestive heart failure in some patients. May be linked to an increased risk of bladder cancer Counseling Point for the Drug Class Report signs and symptoms of liver dysfunction and/or shortness of breath immediately Members of the Drug Class In this section: Pioglitazone Others: Rosiglitazone Pioglitazone Actos Pioglitazone Initial dose: 15 30 mg once daily without regard to meals Limit initial dose to 15 mg once daily in patients with NYHA class I and II heart failure Maintenance dose: 15 45 mg once daily Maximum recommended dose: 15 mg once daily in patients taking strong CYP2C8 inhibitors (e.g., gemfibrozil) 38 CHAPTER 2 Antidiabetic Agents

REVIEW QUESTIONS 1. Which of the following medications has a warning about a rare but serious metabolic complication called lactic acidosis? a. Sitagliptin b. Metformin c. Exenatide d. Pioglitazone 2. What is the maximum daily dose of immediate-release metformin? a. 1000 mg b. 1500 mg c. 2000 mg d. 2550 mg 3. A patient s GFR is 20 ml/min; what is the starting dose of metformin? a. 500 mg BID b. 1000 mg BID c. 2000 mg once daily d. Use is contraindicated 4. What is the mechanism of action of dapagliflozin? a. Inhibits di-peptidyl peptidase-4 b. Inhibits sodium-glucose Cotransporter-2 c. Acts as a direct GLP-1 agonist d. Stimulates insulin release from the pancreas 5. Which of the following is a brand name of exenatide? a. Farxiga b. Jardiance c. Bydureon d. Victoza 6. Which class of drugs may cause decreased bone mineral density and bone fractures? a. Biguanide b. GLP-1 agonist c. SGLT-2 inhibitor d. Sulfonylurea 7. Which of the following drugs can be used in a patient with a GFR of < 30 ml/min? a. Liraglutide b. Exenatide c. Metformin d. Canagliflozin 8. Acute pancreatitis has been reported with which of the following drugs? a. Sitagliptin b. Metformin c. Basaglar insulin d. Glipizide XL 9. Which of the following is a proper counseling point for a patient taking metformin? a. Temporarily withhold in patients undergoing radiologic procedures involving iodinated contrast b. Use proper SUB-Q injection technique c. Monitor for urinary tract infections d. Monitor for signs and symptoms of acute pancreatitis 10. Before initiating, which of the following should you perform spirometry (FEV1)? a. Liraglutide b. Basaglar insulin c. Exenatide d. Afrezza 11. What is the typical starting dose of empagliflozin? a. 5 mg b. 10 mg c. 25 mg d. 100 mg 12. Which of the following is NOT a brand name for insulin glargine? a. Toujeo b. Lantus c. Apidra d. Basaglar 13. Which of the following is the average HbA1c reduction with sulfonylureas? a. 0.7 1% b. 1 1.5% c. 1 2 % d. 1.5 2% 14. Which of the following medications can be dosed once weekly? a. Lantus b. Toujeo c. Afrezza d. Victoza 15. What is the correct dose of sitagliptin in a patient with a GFR of 40 ml/min? a. 100 mg b. 50 mg c. 25 mg d. Use is contraindicated 16. Inhibition of di-peptidyl peptidase-4 is the mechanism of action of which drug? a. Glimepiride b. Metformin c. Insulin d. Sitagliptin 2 Antidiabetic Agents Review Questions 39

17. Insulin inhalation powder is most closely related to which insulin? a. Aspart b. Regular c. NPH d. Detemir 18. All of the following are counseling points regarding insulin EXCEPT a. Rotate injection sites to prevent lipodystrophy b. Wear diabetic identification c. Mild episodes of hypoglycemia should be treated with glucagon d. Insulin stored at room temperature will be less painful 19. All of the following are rapid-acting insulins EXCEPT a. Lispro b. Glulisine c. Aspart d. Detemir 20. Which of the following has been used to treat antipsychotic-induced weight gain? a. Glyburide b. Pioglitazone c. Metformin d. NPH insulin 21. Which class of drugs has rare but serious side effects of arthralgia, bullous pemphigoid, and Stevens-Johnson syndrome? a. Biguanide b. Sulfonylurea c. DPP-4 inhibitor d. SGLT-2 inhibitor 22. Which drug needs to be avoided in a patient with a personal or family history of medullary thyroid carcinoma? a. Canagliflozin b. Glipizide c. Exenatide d. Pioglitazone 23. When a patient is stable on a current dose of insulin, how often should you check the HbA1c? a. Weekly b. Monthly c. Every 6 months d. Every 2 years 24. Hypoglycemia, cough, and throat irritation are side effects of which of the following? a. Afrezza b. Apidra c. Humalog d. NovoLog 25. Which insulin is commercially available in 200 units/ml? a. Aspart b. Lispro c. Glargine d. Detemir 26. Which class of drugs has a rare but serious side effect of causing ketoacidosis? a. SGLT-2 inhibitor b. GLP-1 agonist c. Biguanide d. Insulin 27. What is the maximum recommended dose of Invokana in a patient with a GFR of 80 ml/min? a. 50 mg b. 100 mg c. 250 mg d. 300 mg 28. Humalog Mix 75/25 contains which of the following? a. 75% rapid-acting lispro and 25% intermediateacting lispro suspension b. 25% rapid-acting lispro and 75% intermediate- acting lispro suspension c. 75% regular insulin and 25% NPH insulin d. 25% regular insulin and 75% NPH insulin 29. Toujeo is available in which of the following concentrations? a. 100 units/ml b. 300 units/ml c. 500 units/ml d. Both a and b are correct 30. Which of the following statements regarding Bydureon is FALSE? a. It is a GLP-1 agonist b. It is administered as a SUB-Q injection c. It is dosed twice daily d. It has a rare but serious side effect of acute pancreatitis 40 CHAPTER 2 Antidiabetic Agents