Physostigmine: Difference between revisions

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==Pharmacology==
==Pharmacology==
*Half-life:
*Reversible AChE inhibitor, that increases concentration of acetylcholine
*Metabolism:
*Indirectly stimulates both nicotinic and muscarinic ACh receptors
*Excretion:
*Metabolism via CYP450
*Mechanism of Action:
*Excretion minimally via urine
*Onset of action: 15-20min
*Onset of action: 15-20min



Revision as of 19:52, 7 October 2018

General

Adult Dosing

Anticholinergic toxicity

  • 0.5-2mg IV over 5min

Pediatric Dosing

  • .02mg/kg repeat every 5-10 minutes until adequate response, max of 2mg
  • no faster than .5mg/min

Special Populations

  • Pregnancy Rating:
  • Lactation:
  • Renal Dosing
    • Adult
    • Pediatric
  • Hepatic Dosing
    • Adult
    • Pediatric

Contraindications

  • Allergy to class/drug

Adverse Reactions

  • Side effects: bradycardia, dysrhythmias, cholinergic excess
    • Always have atropine at the bedside for bradycardia or cholinergic excess

Pharmacology

  • Reversible AChE inhibitor, that increases concentration of acetylcholine
  • Indirectly stimulates both nicotinic and muscarinic ACh receptors
  • Metabolism via CYP450
  • Excretion minimally via urine
  • Onset of action: 15-20min

See Also

References