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Neostigmine Methylsulfate Injection, USP (Jamp Pharma) Product Monograph

Status:
Prescription (Rx) Facts
Strength:
0.5 mg
Active ingredient:
Similar drugs:

Product Monograph - Neostigmine Methylsulfate Injection, USP (Jamp Pharma)

SYMPTOMS AND TREATMENT OF OVERDOSAGE

Symptoms: Muscarinic and nicotinic effects (see ADVERSE REACTIONS). Distinguish from myasthenic crisis with edrophonium chloride, if necessary.

Treatment: Control muscarinic effects with IV atropine, followed by intramuscular (IM) atropine every 2 to 4 hours. Assist ventilation and treat convulsions or shock if necessary.

For management of a suspected drug overdose, contact your regional poison control centre.

DOSAGE AND ADMINISTRATION

Intestinal atony, postoperative: Prophylaxis: 250 mcg subcutaneous (SC) or IM before or immediately after operation, repeated every 4 to 6 hours SC. Treatment: 500 mcg SC, IM (or possibly IV) repeated at intervals of 4 to 5 hours.

Urinary Retention: Prophylaxis: 250 mcg as for intestinal atony. Treatment: 500 mcg SC or IM and apply heat to the lower abdomen. If urination does not occur within one hour, the patient should be catheterized. After the patient has voided, continue the 500 mcg injections at 3-hour intervals for at least 5 additional injections.

Curare Antagonist (to neutralize the effect of curare in surgical anesthesia and shock therapy): 0.5 to 2 mg IV. Atropine sulfate 0.6 to 1.2 mg IV should also be given.

DOSAGE FORMS, COMPOSITION, AND PACKAGING

Neostigmine Methylsulfate Injection, USP is a clear, colourless solution. Each mL contains neostigmine methylsulfate 0.5 mg and the following non-medicinal ingredients: acetic acid for pH adjustment, phenol 4.5 mg as preservative, sodium acetate trihydrate 0.2 mg as a buffer and sodium hydroxide for pH adjustment and water for injection. Available in 10 mL clear glass vials (Multidose), 10 vials per carton.

STORAGE AND STABILITY

Store between 15- 30°C. Protect from light. Multi-dose. Discard 28 days after initial use.

Do not use product if mixture (solution) shows haziness, particulate matter, discolouration, or leakage.

REFERENCES

  1. 1)

    NEOSTIGMINE OMEGA (Neostigmine Methylsulfate Injection USP), Prescribing

    Information, Omega Laboratories Limited, Date of revision: November May 24, 2012.

If you want more information about Neostigmine Methylsulfate Injection, USP:

  • Talk to your healthcare professional
  • Find the full Product Monograph that is prepared for healthcare professionals and includes the Patient Medication Information by visiting the Health Canada website: (https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/drug-product-database.html); the manufacturer’s website (www.jamppharma.com), or by calling at 1-866-399-9091.

JAMP Pharma Corporation

1310 rue Nobel

Boucherville, Quebec

J4B 5H3, Canada

Last Approved: April 26, 2023

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02537516

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Neostigmine Methylsulfate Injection, USP (Jamp Pharma)

Rx or OTC
Prescription (Rx)?
DIN 02537516
Schedule(s) PRESCRIPTION
Active ingredient(s) Neostigmine methylsulfate 0.5 MG
Dosage form(s) Solution
Route(s) of administration Subcutaneous, Intramuscular, Intravenous
Drug class (WHO ATC)
  1. N Nervous system drugs
    1. N07 Other nervous system drugs
      1. N07A Parasympathomimetics
        1. N07AA Anticholinesterase parasympathomimetics
          1. N07AA01 Neostigmine
Company JAMP PHARMA CORPORATION
Current status Marketed
Current status date March 28, 2024

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.