Finished product reference

Pralidoxime Iodide

Injection, Solution · Parenteral · 25 mg/1 mL · 20 mL

List code
53051
Pharmacologic class
Cholinesterase reactivator (oxime antidote)

What it is and how it works

Pralidoxime binds to organophosphate-inhibited acetylcholinesterase and removes the phosphoryl group, restoring enzyme activity, mainly at nicotinic sites (reversing muscle weakness and paralysis). It is effective only before ‘ageing’ of the inhibited enzyme and is used together with atropine, which controls muscarinic effects.

Indications

Adjunct to atropine in the treatment of poisoning by organophosphorus insecticides and nerve agents.

Dosage and administration (summary)

Given by slow intravenous injection or infusion as early as possible; a commonly used regimen (WHO) is a loading dose of about 30 mg/kg followed by a continuous infusion of about 8 mg/kg/hour, adjusted to clinical response.

Contraindications

Hypersensitivity to pralidoxime; the iodide salt should be avoided in patients with iodine hypersensitivity.

Warnings and precautions

Rapid injection may cause tachycardia, laryngospasm, muscle rigidity and hypertension; reduce dose in renal impairment. It is of little value in carbamate poisoning, and the iodide content may affect thyroid function with prolonged use.

Pregnancy

Should be used in pregnancy when needed for life-threatening poisoning.

Storage and supply

Store below 25 °C, protected from light.

Source: reference summary prepared from the EU SmPC/EPAR, BNF and WHO Model Formulary. The approved product information in Iran governs.

Reference information for professional sourcing and registration enquiries, not medical advice or a promotion. Drug information is condensed from US FDA prescribing information (public domain, via openFDA and DailyMed) and does not replace the product’s approved labelling in Iran. Availability, origin and documentation are confirmed per enquiry.

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