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

Naloxon Hcl Accord

Active Ingredient:
Naloxone Hydrochloride
Origin:
EU

Naloxon Hcl Accord (Naloxone Hydrochloride)

Naloxone Hydrochloride, the active ingredient in Naloxon Hcl Accord, is an opioid antagonist presented as an injectable solution for intravenous use. It rapidly reverses opioid‑induced respiratory depression and sedation in patients experiencing an opioid overdose and is indicated for emergency treatment in pre‑hospital and hospital settings.

GNH India supplies Naloxon Hcl Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides full regulatory documentation for global distribution.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Naloxone Hydrochloride acts on the opioid receptor pathway to counteract opioid toxicity.

  • Opioid overdose: quickly restores normal breathing and consciousness in patients with life‑threatening opioid intoxication.
  • Opioid‑induced respiratory depression: reverses suppressed respiration during procedural sedation or chronic opioid therapy.
  • Emergency opioid toxicity: provides immediate antagonism in pre‑hospital or hospital emergency settings.

How It Works

  • Naloxone Hydrochloride is a competitive antagonist that binds preferentially to mu‑opioid receptors, displacing opioid agonists and blocking their activation. By preventing opioid‑mediated inhibition of the brainstem respiratory centers, it restores normal respiratory drive and reverses central nervous system depression without activating the receptors itself.

Side Effects

Naloxone is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Injection site pain: mild discomfort at the site of intravenous administration.
  • Nausea: transient feeling of queasiness.
  • Vomiting: occasional emesis following reversal of opioid effects.
  • Sweating: increased perspiration during recovery.
  • Restlessness: brief agitation as opioid effects wear off.
  • Headache: mild headache in some patients.

Serious or Rare Side Effects

  • Acute withdrawal syndrome: severe agitation, hypertension, tachycardia, or seizures in opioid‑dependent individuals.
  • Cardiac arrhythmias: rare cases of irregular heart rhythm.
  • Hypotension: sudden drop in blood pressure.
  • Pulmonary edema: rare fluid accumulation in the lungs.
  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.

Precautions & Warnings

Naloxone should be used with awareness of specific safety considerations.

  • Patient assessment: evaluate for opioid dependence and potential for precipitated withdrawal.
  • Monitoring: observe vital signs and respiratory status continuously after administration.
  • Contraindications: avoid use in patients with known hypersensitivity to naloxone.
  • Co‑administration: be prepared to provide supportive care for severe withdrawal symptoms.
  • Storage: Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Naloxone may interact with other medications that affect the central nervous system.

Major Interactions (Avoid)

  • Opioid agonists: concurrent high‑dose opioids can diminish reversal effectiveness.
  • Central nervous system depressants: may mask residual sedation after naloxone.

Moderate Interactions (Monitor Closely)

  • Benzodiazepines: monitor for additive respiratory depression.
  • Tricyclic antidepressants: watch for altered cardiovascular response.
  • Anticholinergic agents: assess for increased risk of agitation or delirium.

Frequently Asked Questions

Naloxon Hcl Accord contains naloxone hydrochloride, an opioid antagonist used to rapidly reverse the effects of opioid overdose, including respiratory depression and loss of consciousness, in emergency medical situations.

Naloxone competitively binds to mu‑opioid receptors, displacing opioid molecules and blocking their activity. This restores normal respiratory drive and consciousness by preventing opioids from suppressing the brainstem respiratory centers.

The specific dose and administration schedule are determined by the prescribing clinician based on the patient’s condition, the type of opioid involved, and the clinical setting. Dosing is individualized and should follow local protocols.

Safety data for naloxone in pregnancy and lactation are limited, and the pregnancy category is listed as unknown. The drug should be used only if the potential benefit justifies any potential risk to the fetus or infant, and under medical supervision.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request trade or institutional credentials before providing pricing, availability, shipping details (including any cold‑chain requirements), and import documentation.

Naloxon Hcl Accord is a standard formulation of naloxone, the most widely used opioid antagonist. Compared with alternatives such as nalmefene, naloxone has a faster onset of action and is the preferred agent for emergency reversal of opioid toxicity in most clinical guidelines.

The product should be stored at 2‑8 °C, kept refrigerated, protected from light, and must not be frozen or shaken. Maintain the original packaging until use to preserve stability.

Naloxon Hcl Accord is administered intravenously. The solution is injected directly into a vein, typically as a rapid bolus, and may be repeated if respiratory depression persists, following the clinician’s assessment.

The most serious risks include precipitating acute opioid withdrawal, which can cause severe agitation, hypertension, tachycardia, or seizures, and rare events such as cardiac arrhythmias, hypotension, pulmonary edema, or anaphylactic reactions.

Naloxon Hcl Accord should not be given to individuals with a known hypersensitivity to naloxone or any of its excipients. Caution is advised in patients with severe cardiovascular disease or those at high risk for acute withdrawal.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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