DrugInfoSys

Pralidoxime

Drug #593

Pralidoxime is a cholinesterase reactivator. Chemically Pralidoxime is 2-formyl-1-methylpyridinium. Pralidoxime is used as an antidote to reverse muscle paralysis resulting from organophosphate anticholinesterase pesticide poisoning. Because it does not significantly relieve depression of the respiratory center or decrease the muscarinic effects of anticholinesterase poisoning, atropine must be administered concomitantly to block the effects of the poison on these areas. Pralidoxime is also used to reverse the effects of overdosage of anticholinesterase agents used in the treatment of myasthenia gravis, i.e., neostigmine, pyridostigmine and ambenomium.

Primary Characteristics

It is of Synthetic origin and belongs to Pyridine.

It belongs to Cholinesterase reactivator pharmacological group on the basis of mechanism of action and also classified in Antidotes pharmacological group.

Molecular Weight: 172.6 · pKa: 8.0 · Solubility in Water: 1 in 20 · Solubility in Alcohol: 1 in 100 · Non-proprietary name: Pralidoxime · pH: 4.6 · Isotonic value: 2.87.

Molecular structure of Pralidoxime

Pharmacokinetics

Absorption: Pralidoxime has an oral bioavailability is 22.5% (±7.5%).

Distribution: Pralidoxime has a volume of distribution is 0.6 l/kg. plasma protein binding is negligible.

Elimination: it is metabolised via Hepatic, plasma half-life is 75 min, renal excretion is extensive.

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Indications

Pralidoxime is primarily indicated in conditions like Poisoning of organophosphate.

Contraindications

Pralidoxime is contraindicated in conditions like Myasthenia gravis.

Dosage

Pralidoxime's dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
0.04 mg/kg0.04 mg/kgEvery 0.5hIM -
0.04 mg/kg0.04 mg/kgEvery 0.5hIV -
2.14 mg/kg.min2.14 mg/kg.minIV Inf For 15-30 Minutes
Paediatric Dosage (20kg)
40 mg/kg40 mg/kgSlow IV Single Dose, can be repeated As Required
Neonatal Dosage (3kg)
40 mg/kg40 mg/kgSlow IV Single Dose, can be repeated As Required

Drug Interactions

Unknown5 interactions

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Pralidoxime in overdosage may give rise to further complications which include Excitement , Mania .

Pralidoxime is known to cause more or less tolerable side effects which are usually transient. These include Blurred vision, Diplopia, Disturbances of accomodation, Dizziness, Headache, Heaviness of eye, Hyperventilation , Muscular weakness, Nausea, Tachycardia.

Warnings / Precautions

Caution in required in administering pralidoxime to patients with myasthenia gravis, as it may precipitate a myasthenia crisis. Pralidoxime should be used cautiously in patients with impaired renal function, reduction in dose may be necessary. It should not be used to treat poisoning by carbamate pesticides. Avoid concurrent use with atropine.

Interference in Pathology

Pralidoxime may interfere in the diagnosis of Elevations of SGPT and SGOT .

Available Brands

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Single Ingredient

Storage Conditions

Pralidoxime should be stored IV Inj, IV Inf, IM Inj , SC Inj.

Drug Classification

  1. 1.4.2.3Organophosphate and carbamate poisoning

Manufacturers

Manufacturers of Pralidoxime in Pakistan: