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Drug class | Mechanism of action | Indication | Side effects | Contraindications | Weight impact |
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Biguanides (metformin) | (i) Increases peripheral insulin sensitivity and enhances insulin effects (ii) Reduces LDL and increases HDL | Drug of choice in almost all patients with T2DM | (i) Lactic acidosis (ii) GI distress: nausea, vomiting, diarrhea, and abdominal pain (iii) Vitamin B12 deficiency | (i) Renal failure (ii) Severe liver failure (iii) Chronic pancreatitis (iv) Shock (v) Sepsis | Promotes weight loss |
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SGLT-2 inhibitors (dapagliflozin, and empagliflozin) | (i) Decrease in glucose reabsorption by inhibiting SGLT-2 receptor in the kidney | Treatment-compliant patients with T2DM | (i) Urinary tract infections (ii) Dehydration (iii) Diabetic ketoacidosis | (i) Renal failure (ii) Patients with renal tract abnormalities | Promotes weight loss |
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GLP-1 receptor agonist (exenatide, liraglutide, and dulaglutide) | (i) Increased insulin secretion (ii) Decreased glucagon secretion (iii) Delayed gastric emptying | Treatment-compliant patients with T2DM | (i) GI distress: nausea and vomiting (ii) Increased risk of pancreatitis | (i) Pre-existing gastrointestinal motility disorders (ii) Chronic pancreatitis (iii) Medullary thyroid cancer or MEN2 | Promotes weight loss |
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DPP-4 inhibitors (sitagliptin, saxagliptin, and linagliptin) | (i) Inhibits degradation of DPP4 (ii) Increased insulin secretion (iii) Decreased glucagon secretion (iv) Delayed gastric emptying | Treatment-compliant patients with T2DM | (i) GI distress: diarrhea and constipation (ii) Increased risk of pancreatitis (iii) Worsening renal function (iv) Headaches, dizziness | (i) Liver failure (ii) Renal failure | No significant weight changes |
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Thiazolidinediones (pioglitazone and rosiglitazone) | (i) Activation of the transcription factor PPARγ (ii) Increased glucose utilization (iii) Increased fat storage (iv) Decreased hepatic glucose production | T2DM patients with renal failure and/or contraindications to insulin therapy | (i) Increased risk of heart failure (ii) Osteoporosis (iii) Fluid retention | (i) Congestive heart failure (ii) Liver failure | Promotes weight gain |
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Sulfonylureas (glimepiride, glyburide, and glipizide) | (i) Inhibits ATP-sensitive potassium channels in the pancreas leading to increased insulin secretion (ii) Increased insulin sensitivity (iii) Decreased gluconeogenesis | T2DM patients who have normal BMI and do not consume alcohol | (i) Life-threatening hypoglycemia (ii) Renal failure (iii) Alcohol intolerance (iv) Hemolytic anemia | (i) Beta-blockers (ii) Obesity (iii) Severe liver or renal failure (iv) Sulfonamide allergy (v) Cardiovascular comorbidities | Promotes weight gain |
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Alpha-glucosidase inhibitors (acarbose and miglitol) | (i) Inhibit alpha glucosidase (ii) Delayed glucose absorption (iii) Decreased carbohydrate breakdown and no risk of hypoglycemia | Treatment-compliant patients with T2DM | (i) GI distress: flatulence, bloating, abdominal pain, and diarrhea | (i) Renal failure (ii) Inflammatory bowel disease | No significant weight changes |
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Statin (atorvastatin, rosuvastatin, and simvastatin) | (i) Inhibits HMG-CoA reductase enzyme reducing cholesterol synthesis (ii) Upregulates LDL receptors | Treatment of hypercholesterolemia, hyperlipoproteinemia, and hypertriglyceridemia | (i) Myopathy (ii) Rhabdomyolysis (iii) Hepatotoxicity (iv) Increased risk of developing T2DM | (i) Active hepatic disease (ii) Breastfeeding (iii) Other CYP450 inhibitors | Promotes weight gain |
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Cholesterol absorption inhibitors (ezetimibe) | (i) Inhibit the intestinal absorption of dietary and biliary cholesterol (ii) Lowers LDL-C, modestly decreases triglycerides, and raises HDL-C | Primary hypercholesterolemia | (i) Myopathy (ii) Hepatotoxicity | (i) Hypersensitivity to any component of formulation (ii) Unexplained persistent elevation in serum transaminases | No significant weight changes |
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