Diabetes medications: Difference between revisions

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===Dose===
===Dose===
Metformin 500mg PO BID is first-line agent for type II diabetics
Metformin 500mg PO BID is first-line agent for type II diabetics
*Do not prescribe if Cr > 1.4 (GFR <40), CHF, hepatic insufficiency, ETOH abuse
*Do not prescribe if creatinine > 1.4 (GFR <40), CHF, hepatic insufficiency, ETOH abuse
*Should be withheld for 48hr after IV contrast
*Should be withheld for 48hr after IV contrast
===Side Effects===
===Side Effects===

Revision as of 07:37, 11 August 2016

Background

  • Hypoglycemics
    • Sulfonylureas
    • Benzoic acid derivatives
  • Antihyperglycemics
    • Biguanides
    • Alpha glucosidase inhibitors
    • Thiazolidinediones

Common Anti-hyperglycemic Drugs and Pharmacology

Drug Pharmacology
Onset Peak Duration
Rapid-acting insulin

  • Aspart (Novolog)
  • Lispro (Humalog)
15-30min 1-2h 3-5h
Short-acting insulin

  • Regular
30-60min 2-4h 6-10h
Intermediate-acting insulin

  • NPH (Humulin, Novolin)
1-3h 4-12h 18-24h
Long-acting insulin

  • Glargine (Lantus)
2-4h None 24h
Sulfonylurea

  • Glimepiride
  • Glipizide (Glucotrol)
  • Glyburide (Glycron, Micronase)
2-6h 12-24h

See also GLP-1 agonists

Insulin

Biguanides (Metformin)

Suppresses liver glucose production

Dose

Metformin 500mg PO BID is first-line agent for type II diabetics

  • Do not prescribe if creatinine > 1.4 (GFR <40), CHF, hepatic insufficiency, ETOH abuse
  • Should be withheld for 48hr after IV contrast

Side Effects

  • Lactic acidosis (due to increased lactate production)
    • Seen almost exclusively in patients with renal failure
  • Nausea, diarrhea, crampy abdominal pain

Toxicity

  • Almost never causes hypoglycemia when taken alone, but can exacerbate hypoglycemia when taken in combination with hypoglycemic agents
  • Toxic dose unknown
  • Management: Supportive care

Sulfonylureas

  • Increases insulin secretion (glipizide, glyburide)
  • Hypoglycemia is the major adverse effect (esp with glyburide)

Alpha Glucosidase Inhibitors

  • acarbose, miglitol, voglibose
  • competitively and reversibly inhibit alpha glucosidase brush border hydrolase enzyme- makes postprandial decrease in carbohydrate absorption since complex polysaccharides not broken down into absorbable monosaccharides
  • does not affect lactose absorption
  • if hypoG- sucrose/ table sugar will not work- use glucose- PO or IV
  • taken with first bite of each meal
  • since limited absorption, stays in gut and side effects mostly GI- bloating, gas, diarrhea
  • contraindications- cirrhosis, IBD, malabsorption synd
  • alpha glucs do not cause hypoG when used as monotreatment
  • acarbose- can cause transaminitis/ liver inj
  • since minimal absorption- systemic toxicity from OD unlikely

Thiazolidinediones

  • rosiglitazone and poiglitazone
  • enhance insulin effect on muscle, fat, liver without increasing panc insulin secretion
  • protein bound and hep metab- not good if liver disease
  • side effects- induce ovulation, decrease effectiveness of OCP's, increase plasma volume (bad if CHF)

Benzoic Acid Derivatives

  • repaglinide- mono or combined with metformin
  • binds to ATP dependent potassium channel like sulfonyls but at different site.
  • Unlike sulfonyls, it decreases insulin lvls
  • Dose 30 min before meal to decrease post prandial hyperglycemia

See Also

References