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Pralidoxime

2-PAM

Pralidoxime ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Pralidoxime ballicule

What it isOxime reactivating acetylcholinesterase; organophosphate poisoning.

Why this oneIt reverses nicotinic weakness, including respiratory muscle paralysis, which atropine cannot touch.

What limits itGive it before the enzyme ages; it supplements atropine and is generally not useful in carbamate poisoning.

Pralidoxime molecular structure (skeletal formula)
Molecular structure: Pralidoxime

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Organophosphate poisoning (IV, with atropine)Adults20–50 mg/kg IV over 15–30 min (max 2000 mg/dose)Repeat / continuous infusion as neededInfusion rate ≤200 mg/min
Organophosphate poisoning (IM auto-injector)Adults600 mg IM for mild symptomsRepeat q15min PRN1800 mg (3×600 mg) for severe
Organophosphate poisoning (IM)Peds <40 kg15 mg/kg IM per injectionRepeat PRN45 mg/kg (3-injection course)
Anticholinesterase overdose in myasthenia gravisAdults1000–2000 mg IVThen 250 mg q5min

Renal Undefined

Hepatic Undefined

Additional doses may be needed q3–8 h if signs of poisoning recur; observe patient 48–72 h

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy No animal studies; give only if clearly needed

Lactation Undefined

Cost

Pralidoxime (2-PAM)
Strength#/mogeneric $/unitCostPlus
1 ginjper unitnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Pralidoxime is administered under clinical supervision and dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

NO BOXED WARNINGS

Principal riskUseless once the enzyme has aged, and in carbamates

Classes and tags

Clinical profile

Therapeutic safety burden3 / 4
Overdose danger3 / 4
Weight-gain liability0 / 4
Sedation liability1 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4

Legacy pregnancy categoryC

Defining liabilityRapid-infusion cardiopulmonary toxicity

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