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

Naltrexone Accord

Active Ingredient:
Naltrexone Hydrochloride
Origin:
EU

Naltrexone Accord (Naltrexone Hydrochloride)

Naltrexone Hydrochloride, the active ingredient in Naltrexone Accord, is an opioid antagonist presented as a tablet for oral use. It is used to support treatment of alcohol and opioid dependence in adults.
GNH India supplies Naltrexone Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Naltrexone Accord is an opioid antagonist indicated for managing substance dependence disorders.

  • Alcohol dependence: helps reduce cravings and supports abstinence from alcohol.
  • Opioid dependence: blocks opioid receptors to prevent relapse and reduce the rewarding effects of opioids.
  • Substance use disorder: used as part of a comprehensive treatment program to maintain sobriety.

How It Works

  • Naltrexone Hydrochloride acts as a competitive antagonist at mu, kappa, and delta opioid receptors. By binding to these receptors without activating them, it blocks the effects of both endogenous opioids and exogenous opioid substances, thereby reducing reinforcement, craving, and the physiological response associated with opioid and alcohol use.

Side Effects

Naltrexone Accord may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Headache: transient cranial pain.
  • Dizziness: sensation of light‑headedness.
  • Fatigue: general tiredness.
  • Insomnia: difficulty falling or staying asleep.
  • Vomiting: occasional emesis.

Serious or Rare Side Effects

  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Severe depression: mood changes requiring medical attention.
  • Suicidal thoughts: emergence of suicidal ideation.
  • Allergic reactions: rash, itching, or swelling.
  • Liver failure: rare but life‑threatening hepatic dysfunction.

Precautions & Warnings

Before initiating therapy with Naltrexone Accord, consider the following precautions.

  • Liver function assessment: evaluate hepatic enzymes prior to use.
  • Depression monitoring: watch for worsening mood or suicidal thoughts.
  • Acute opioid withdrawal: avoid initiating during active withdrawal to prevent precipitated symptoms.
  • Renal impairment: adjust use in patients with severe kidney disease.
  • Hypersensitivity: discontinue if allergic reaction occurs.
  • Store at room temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Naltrexone Accord can interact with several medications, requiring careful management.

Major Interactions (Avoid)

  • Opioid agonists (e.g., morphine, oxycodone): may precipitate withdrawal.
  • Methadone or buprenorphine: can reduce therapeutic effect and cause abrupt withdrawal.
  • Disulfiram: combined hepatotoxic risk.

Moderate Interactions (Monitor Closely)

  • CNS depressants (e.g., benzodiazepines): may enhance sedation.
  • Antidepressants (e.g., SSRIs): monitor for mood changes.
  • Rifampin: may increase naltrexone metabolism, reducing efficacy.

Frequently Asked Questions

Naltrexone Accord contains naltrexone hydrochloride, an opioid antagonist prescribed to help individuals with alcohol dependence or opioid dependence maintain abstinence and reduce cravings as part of a comprehensive treatment plan.

Naltrexone binds competitively to mu, kappa, and delta opioid receptors without activating them, blocking the effects of both endogenous opioids and external opioid substances. This inhibition reduces the rewarding sensations associated with alcohol and opioid use, supporting recovery.

The specific dose and dosing schedule for Naltrexone Accord are determined by the prescribing healthcare professional based on the patient’s condition, treatment goals, and clinical response. Patients should follow the prescriber’s instructions exactly.

Safety data for naltrexone use in pregnancy and lactation are limited. Healthcare providers should weigh potential benefits against possible risks and consider alternative therapies when treating pregnant or nursing individuals.

To request Naltrexone Accord, 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 any necessary import documentation.

Naltrexone is a non‑opioid antagonist, differing from opioid agonist therapies such as methadone or buprenorphine, which activate opioid receptors. Naltrexone blocks receptor activity, eliminating opioid effects, whereas agonist therapies replace opioid activity to reduce withdrawal. Choice depends on patient preference, clinical profile, and treatment setting.

Store Naltrexone Accord at room temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture and direct sunlight, and ensure the container is tightly closed to maintain product stability.

Naltrexone Accord is taken orally, usually as a tablet, with or without food as directed by the prescriber. Patients should swallow the tablet whole and avoid crushing or chewing unless instructed otherwise.

Serious risks include hepatotoxicity, severe depression, and suicidal thoughts. Patients should be monitored regularly for liver function abnormalities and changes in mood, and any concerning symptoms should prompt immediate medical evaluation.

Naltrexone Accord should not be used by individuals with acute opioid withdrawal, severe hepatic impairment, known hypersensitivity to naltrexone, or those currently taking opioid analgesics without appropriate medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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