Product image of Naloxone Accord (Naloxone Hydrochloride) supplied by GNH India

Naloxone Accord

Active Ingredient:
Naloxone Hydrochloride
Origin:
EU

Naloxone Accord (Naloxone Hydrochloride)

Naloxone, the active ingredient in Naloxone Accord, is an opioid antagonist presented as an injectable solution for intravenous use. Classified under ATC code N07BC01, it is employed to rapidly reverse the respiratory and central nervous system depression caused by opioid overdose in both adult and pediatric patients.

GNH India supplies Naloxone Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to this essential antidote for emergency and critical care settings.

Manufacturer / TM Owner

Accord Healthcare Polska Sp. Z O.O.

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Indications & Clinical Uses

Naloxone is an opioid antagonist used in the management of opioid overdose and related conditions.

  • Opioid overdose: restores normal respiration and consciousness by displacing opioids from μ‑receptors.
  • Opioid‑induced respiratory depression: rapidly reverses life‑threatening respiratory depression.
  • Opioid toxicity: counteracts central nervous system depression and sedation caused by opioid exposure.

How It Works

  • Naloxone acts as a competitive antagonist at μ, κ and δ opioid receptors. By binding to these receptors without activating them, it displaces opioid agonists such as morphine, fentanyl or heroin, thereby reversing their pharmacologic effects on respiratory drive, analgesia, and central nervous system depression.

Side Effects

Naloxone may cause a range of adverse reactions after administration.

Common Side Effects

  • Injection site pain: mild discomfort at the site of intravenous administration.
  • Nausea: transient feeling of queasiness.
  • Sweating: increased perspiration.

Serious or Rare Side Effects

  • Acute pulmonary edema: sudden fluid accumulation in the lungs.
  • Seizures: convulsive episodes, especially in patients with pre‑existing seizure disorders.
  • Anaphylaxis: severe allergic reaction requiring immediate medical intervention.

Precautions & Warnings

Naloxone should be used with careful clinical assessment and monitoring.

  • Assess airway and breathing: confirm opioid‑induced respiratory compromise before administration.
  • Monitor cardiovascular status: watch for hypertension or tachycardia after dosing.
  • Consider opioid dependence: abrupt reversal may precipitate withdrawal symptoms.
  • Avoid in patients with known hypersensitivity to naloxone.
  • Pregnancy: use only if the anticipated benefit outweighs potential risk, as safety data are limited.
  • Store at ambient temperature: keep in the original container, protect from light and moisture.

Avoid Interactions

Naloxone may interact with other medications that affect the central nervous or cardiovascular systems.

Major Interactions (Avoid)

  • Potent opioids (e.g., fentanyl): may require higher naloxone doses for effective reversal.
  • Drugs that lower seizure threshold: concurrent use can increase seizure risk.
  • Vasopressors: may mask hypotension caused by opioid toxicity.

Moderate Interactions (Monitor Closely)

  • Benzodiazepines: may need additional support for residual sedation.
  • Anticholinergics: monitor for additive cardiovascular effects.
  • Cardiac glycosides: observe for potential arrhythmias during reversal.

Frequently Asked Questions

Naloxone Accord is used to rapidly reverse the effects of opioid overdose, including respiratory depression and loss of consciousness, by antagonizing opioid receptors in emergency and critical care settings.

Naloxone works as a competitive antagonist at μ, κ and δ opioid receptors, displacing opioid molecules without activating the receptors, which quickly restores normal breathing and alertness.

The dose of Naloxone Accord is determined by the prescribing clinician based on the severity of the overdose, patient weight, and clinical response; no fixed regimen is provided here.

Safety data for naloxone in pregnancy and lactation are limited; it should be used only if the potential benefit justifies any possible risk to the fetus or infant.

To order, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Naloxone Accord is a standard opioid antagonist with a rapid onset of action, similar to other naloxone products. Its intravenous formulation allows immediate delivery, whereas intranasal or auto‑injector forms may have slightly slower absorption.

Store Naloxone Accord at ambient temperature, keeping it in the original packaging, protected from light and moisture. Do not freeze the product.

Naloxone Accord is administered intravenously by a qualified healthcare professional. The solution is injected directly into a vein, allowing rapid distribution to opioid‑blocked receptors.

Serious risks include acute pulmonary edema, seizures, severe hypertension, and rare anaphylactic reactions. Immediate medical monitoring is essential after administration.

Patients with a known hypersensitivity to naloxone or any component of the formulation should not receive Naloxone Accord. Use in individuals without opioid exposure should be avoided.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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