Diazoxide: Difference between revisions

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==Background==
==General==
*Type: [[Antihypertensive]], hyperglycemic
*Routes of administration: PO, IV (discontinued in US)
 
*Non-diuretic thiazide, arterial vasodilator
*Non-diuretic thiazide, arterial vasodilator
*Used to treat severe hypertension
*Used to treat severe hypertension
*Reflex response leads to tachycardia and increased cardiac output
*Reflex response leads to tachycardia and increased cardiac output
==Adult Dosing==
*1-3 mg/kg IV (maximum 150 mg)
*3-8 mg/kg/day PO divided into 2-3 doses
==Pediatric Dosing==
*3-8 mg/kg/day PO divided into 2-3 doses
==Special Populations==
*Pregnancy: C
*Lactation: Infant risk cannot be ruled out
*Renal Dosing: reduce dose
*Hepatic Dosing:


==Contraindications==
==Contraindications==
*Aortic stenosis
*Allergy to class/drug
*Aortic coarctation
*Functional hypoglycemia
*Aortic stenosis, aortic coarctation
*Hypertrophic cardiomyopathy
*Hypertrophic cardiomyopathy
==Dosing==
*1-3 mg/kg IV (maximum 150 mg)


==Adverse Effects==
==Adverse Effects==
===Serious===
*CHF, MI
*Pulmonary hypertension
*Fluid retention
*DKA, HHS, hyperglycemia
*Hypernatremia
*Bowel obstruction
*Pancreatitis
*Thrombocytopenia
*Cataract
===Common===
*Hypotension
*Hypotension
*Fluid retention after prolonged use
*Palpitations, tachycardia
*Hyperglycemia
*Dizziness, asthenia
*Hyperglycemia, glycosuria, increased uric acid level
*Hirsutism
*Abdominal pain, nausea/vomiting, diarrhea, anorexia
*Neutropenia


==Interactions==
==Interactions==
*May potentiate warfarin's anticoagulant effects
*May potentiate warfarin's anticoagulant effects


==Pregnancy==
==Pharmacology==
*Class C
*Half-life: 20-36 hours
*Has caused skeletal, cardiac, and pancreatic abnormalities in animals
*Metabolism: hepatic
*Excretion: Renal
 
==Mechanism of Action
*Hyperglycemic: inhibits pancreatic insulin release
*Antihypertensive: arteriolar vasodilation and decreased peripheral resistance


==References==
==References==
Olson, K. Poisoning and Drug Overdose, 1999
Olson, K. Poisoning and Drug Overdose, 1999
Epocrates
Epocrates
[[Category:Pharmacology]]

Latest revision as of 15:51, 22 August 2017

General

  • Type: Antihypertensive, hyperglycemic
  • Routes of administration: PO, IV (discontinued in US)
  • Non-diuretic thiazide, arterial vasodilator
  • Used to treat severe hypertension
  • Reflex response leads to tachycardia and increased cardiac output

Adult Dosing

  • 1-3 mg/kg IV (maximum 150 mg)
  • 3-8 mg/kg/day PO divided into 2-3 doses

Pediatric Dosing

  • 3-8 mg/kg/day PO divided into 2-3 doses

Special Populations

  • Pregnancy: C
  • Lactation: Infant risk cannot be ruled out
  • Renal Dosing: reduce dose
  • Hepatic Dosing:

Contraindications

  • Allergy to class/drug
  • Functional hypoglycemia
  • Aortic stenosis, aortic coarctation
  • Hypertrophic cardiomyopathy

Adverse Effects

Serious

  • CHF, MI
  • Pulmonary hypertension
  • Fluid retention
  • DKA, HHS, hyperglycemia
  • Hypernatremia
  • Bowel obstruction
  • Pancreatitis
  • Thrombocytopenia
  • Cataract

Common

  • Hypotension
  • Palpitations, tachycardia
  • Dizziness, asthenia
  • Hyperglycemia, glycosuria, increased uric acid level
  • Hirsutism
  • Abdominal pain, nausea/vomiting, diarrhea, anorexia
  • Neutropenia

Interactions

  • May potentiate warfarin's anticoagulant effects

Pharmacology

  • Half-life: 20-36 hours
  • Metabolism: hepatic
  • Excretion: Renal

==Mechanism of Action

  • Hyperglycemic: inhibits pancreatic insulin release
  • Antihypertensive: arteriolar vasodilation and decreased peripheral resistance

References

Olson, K. Poisoning and Drug Overdose, 1999 Epocrates