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Pralidoxime

Generic Medicine Info
Indications and Dosage
Intramuscular
Organophosphorus poisoning
Adult: In case IV pralidoxime administration is not feasible as an adjunct to atropine: Mild: 600 mg, may be repeated 1 or 2 times every 15 minutes if symptoms persist. Max total cumulative dose: 1,800 mg. If severe symptoms develop after the 1st dose, may give the 2 additional 600 mg doses in rapid succession for total cumulative dose of 1,800 mg. Severe: Three 600 mg inj given in rapid succession for a total cumulative dose of 1,800 mg. Persistent: May repeat the entire series (three 600 mg inj for total dose of 1,800 mg), starting approx 1 hour after administration of the last inj. Dosage recommendations may vary among individual products and between countries (refer to detailed product or local guidelines).
Child: In case IV pralidoxime administration is not feasible as an adjunct to atropine: Patients weighing <40 kg: Mild: 15 mg/kg/dose, may be repeated 1 or 2 times every 15 minutes if symptoms persist for total cumulative dose of 45 mg/kg. If severe symptoms develop after the 1st dose, may give the 2 additional doses in rapid succession for total cumulative dose of 45 mg/kg. Severe: Three 15 mg/kg/dose inj given in rapid succession for total cumulative dose of 45 mg/kg. Persistent: May repeat the entire series (three 15 mg/kg/dose inj for total dose of 45 mg/kg), starting approx 1 hour after administration of the last inj. ≥40 kg: Same as adult dose. All doses are inj into the anterolateral aspect of the thigh. Dosage recommendations may vary among individual products and between countries (refer to detailed product or local guidelines).

Intravenous
Organophosphorus poisoning
Adult: As adjunct to atropine: Administer as soon as the effects of atropine are observed. Loading dose: 1,000-2,000 mg (diluted to 10-20 mg/mL concentration) via IV infusion over 15-30 minutes. Alternatively, if infusion is not practical or pulmonary oedema occurs, may give the loading dose (diluted to 50 mg/mL concentration) via slow IV inj over at least 5 minutes. Doses may be repeated after 1 hour if muscle weakness is not relieved, then additional doses may be given every 10-12 hours if muscle weakness persists. Max intermittent infusion rate: 200 mg/min. Maintain atropinisation throughout therapy for at least 48 hours; large amount of atropine may be needed concomitantly. Dosage recommendations may vary among individual products and between countries (refer to detailed product or local guidelines).
Child: As adjunct to atropine: Administer as soon as the effects of atropine are observed. ≤16 years Loading dose: 20-50 mg/kg (Max: 2,000 mg/dose) via IV infusion over 15-30 minutes. Maintenance: 10-20 mg/kg/hour via continuous IV infusion. Alternative intermittent infusion dosing: 20-50 mg/kg (Max: 2,000 mg/dose) loading dose via IV infusion over 15-30 minutes. If muscle weakness is not relieved, another 20-50 mg/kg may be given after 1 hour if and may be repeated every 10-12 hours as needed. Max intermittent infusion rate: 200 mg/min. >16 years Same as adult dose. Dosage recommendations may vary among individual products and between countries (refer to detailed product or local guidelines).

Intravenous
Anticholinesterase overdose
Adult: For cases caused by drugs used to treat myasthenia gravis (e.g. neostigmine, pyridostigmine, ambenonium): Initially, 1,000-2,000 mg via IV infusion, followed by 250 mg increments every 5 minutes as necessary. Dosage recommendations may vary among individual products and between countries (refer to detailed product or local guidelines).
What are the brands available for Pralidoxime in Malaysia?
  • Pampara
Renal Impairment
Dose reduction is required.
Reconstitution
Intravenous:
Powder or solution for IV inj: Reconstitute a 1,000 mg vial with 20 mL sterile water for inj to make a 50 mg/mL concentration. For fluid-restricted patients or in case IV inj over 5 minutes is needed, the 50 mg/mL concentration may be given. IV infusion: For other patients, further dilute the reconstituted solution with NaCl 0.9% solution to make a final concentration of 10-20 mg/mL.

Intramuscular:
Powder for IM inj: Reconstitute a 1,000 mg vial with 3.3 mL of sterile water for inj to make a final concentration of approx 300 mg/mL.
Special Precautions
Patient with myasthenia gravis. Not indicated for the treatment of carbamate poisoning and poisoning due to phosphorus, inorganic phosphates, or organophosphates without anticholinesterase activity. Renal impairment. Children. Pregnancy and lactation.
Adverse Reactions
Significant: Precipitation of myasthenic crisis; transient worsening of cholinergic manifestation (e.g. tachycardia, laryngospasm, muscle rigidity or paralysis) if given via rapid IV inj/infusion.
Eye disorders: Blurred vision, diplopia, impaired accommodation.
Gastrointestinal disorders: Nausea, vomiting.
General disorders and administration site conditions: Inj site pain (IM).
Investigations: Increased AST or ALT.
Musculoskeletal and connective tissue disorders: Muscle weakness.
Nervous system disorders: Headache, dizziness, drowsiness.
Respiratory, thoracic and mediastinal disorders: Hyperventilation.
Vascular disorders: Hypertension.
IM/IV/Parenteral/SC: C
Monitoring Parameters
Monitor blood pressure, pulse and heart rate, respiratory rate, muscle fasciculations or strength, changes in consciousness, and fluid balance throughout therapy. Perform continuous ECG and haemodynamic monitoring as required.
Action
Description:
Overview: Pralidoxime is a cholinesterase reactivator.
Mechanism of Action: Pralidoxime reactivates cholinesterase outside the CNS that had been inactivated through phosphorylation due to exposure to certain organophosphate pesticides by displacing the enzyme from its receptor sites. It reverses muscle paralysis by removing the phosphoryl group from the active site of the inhibited enzyme.
Pharmacodynamics: The clinical effects of pralidoxime are most apparent at the skeletal neuromuscular junction, where it relieves anticholinesterase-induced paralysis of respiratory and other skeletal muscles. Pralidoxime does not substantially influence muscarinic effects (e.g. bronchoconstriction, dyspnoea, cough, increased bronchial secretion, salivation); therefore, atropine is given concomitantly to relieve muscarinic symptoms and directly block the effects of accumulated acetylcholine at various sites in the respiratory centre.
Pharmacokinetics:
Absorption: Time to peak plasma concentration: 5-15 minutes (IV); approx 35 minutes (IM).
Distribution: Distributed throughout the extracellular water. Limited CNS distribution.
Metabolism: Metabolised in the liver.
Excretion: Via urine (80% as metabolites and unchanged drug). Elimination half-life: 74-77 minutes (apparent); 3-4 hours (IV or IM doses in poisoned patients).
Chemical Structure

Chemical Structure Image
Pralidoxime

Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 135398747, Pralidoxime. https://pubchem.ncbi.nlm.nih.gov/compound/Pralidoxime. Accessed Oct. 28, 2025.

Storage
Store between 15-30°C.
MIMS Class
Antidotes & Detoxifying Agents
ATC Classification
V03AB04 - pralidoxime ; Belongs to the class of antidotes. Used in the management of organo-phosphate poisoning.
References
Brayfield A, Cadart C (eds). Pralidoxime. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 08/10/2025.

Joint Formulary Committee. Pralidoxime Chloride. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 08/10/2025.

Pampara Injection 500 mg/20 mL (Averroes Pharmaceuticals Sdn. Bhd.). National Pharmaceutical Regulatory Agency - Ministry of Health Malaysia. https://www.npra.gov.my. Accessed 08/10/2025.

Pralidoxime Chloride. UpToDate Lexidrug, AHFS DI (Adult and Pediatric) Online. American Society of Health-System Pharmacists, Inc. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 08/10/2025.

Pralidoxime. Gold Standard Drug Database in ClinicalKey [online]. Elsevier Inc. https://www.clinicalkey.com. Accessed 08/10/2025.

Pralidoxime. UpToDate Lexidrug, Lexi-Drugs Multinational Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 08/10/2025.

Protopam Chloride Injection, Powder, Lyophilized, for Solution (Baxter Healthcare Corporation). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 08/10/2025.

Disclaimer: This information is independently developed by MIMS based on Pralidoxime from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to MIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, MIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2025 MIMS. All rights reserved. Powered by MIMS.com
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