Physostigmine

DEA Class;  Rx

Common Brand Names; 

  • Acetylcholinesterase Inhibitors, Peripheral; 
  • Anticholinergic Toxicity Antidotes
 
 
 
 

Indirect acting parasympathomimetic via inhibition of acetylcholinesterase

For the Anticholinergic Toxicity

Rarely used; indicated only when life-threatening symptoms related to anticholinergic toxicity

Useful for diagnostic as opposed to therapeutic reasons

Salicylate allergy

Asthma, gangrene, diabetes, cardiovascular disease, mechanical obstruction of the intestinal or urogenital tract or any vagotonic state

Concurrency with choline esters or depolarizing neuromuscular blocking agents

Seizure

Cardiovascular collapse

Bradycardia

Bronchospasm

Dyspnea

Diaphoresis

Diarrhea

Hyperperistalsis

Cholinergic Sx

Hallucinations

Overdosage may result in cholinergic crisis (eg, excessive salivation and sweating, miosis, nausea, vomiting, diarrhea, bradycardia or tachycardia, hypotension or hypertension, confusion, seizures, coma, severe muscle weakness, paralysis); if overdosage occurs, mechanical ventilation with repeated bronchial aspiration and IV atropine are recommended

Possible bradycardia, hypersalivation leading to respiratory problems, and/or seizures associated with rapid IV administration; asystole also has been reported; administer at a slow controlled rate

Discontinue therapy if excessive salivation, vomiting, urination, or defecation occurs; reduce dosage if excessive sweating or nausea occurs; atropine sulfate injection should always be readily available; observe patient for evidence of bronchial constriction; perform cardiac monitoring

Use with caution in patients with epilepsy, parkinsonian syndrome, or bradycardia

Pregnancy Category: C

Lacation: Unknown if excreted in breast milk; caution advised

Adults

Initial: 0.5-2 mg slow IVP (not to exceed 1 mg/min); keep atropine nearby for immediate use

If no response, repeat q20min PRN

If initial dose effective, may give additional 1-4 mg q30-60min PRN

Pediatric 

0.02 mg/kg/dose slow IVP (not to exceed 0.5 mg/min); may repeat q5-10min PRN, not to exceed cumulative dose of 2 mg

Injectable solution

  • 1mg/mL

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