Product image of Naltrexon "walter Ritter" (Naltrexone Hydrochloride) supplied by GNH India

Naltrexon "walter Ritter"

Active Ingredient:
Naltrexone Hydrochloride
Origin:
EU

Naltrexon "walter Ritter" (Naltrexone Hydrochloride)

Naltrexone, the active ingredient in Naltrexone "walter Ritter", is an opioid antagonist presented as an oral dosage form for oral use. It is employed in the management of alcohol dependence and opioid dependence in adults.
GNH India supplies Naltrexone "walter Ritter" as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Walter Ritter Gmbh + Co. Kg

1
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Indications & Clinical Uses

Naltrexone is used within the opioid and alcohol dependence therapeutic pathways to reduce relapse risk and diminish rewarding effects of substances.

  • Alcohol dependence: helps maintain abstinence by blocking reinforcing effects of alcohol.
  • Opioid dependence: supports relapse prevention after detoxification by antagonising mu‑opioid receptors.
  • Opioid dependence (maintenance phase): used as an adjunct to psychosocial therapy to reduce cravings.

How It Works

  • Naltrexone acts as a competitive antagonist at opioid receptors, primarily the mu‑opioid subtype. By binding to these receptors without activating them, it blocks the effects of both endogenous opioids and exogenous opioid agonists, thereby diminishing the rewarding and reinforcing properties of alcohol and opioid substances.

Side Effects

Naltrexone may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Headache: transient cranial discomfort.
  • Dizziness: occasional light‑headedness.
  • Fatigue: reduced energy levels.
  • Insomnia: difficulty initiating or maintaining sleep.
  • Abdominal pain: mild stomach discomfort.

Serious or Rare Side Effects

  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Severe depression: mood changes requiring medical attention.
  • Suicidal ideation: thoughts of self‑harm.
  • Allergic reactions: rash, pruritus, or angioedema.
  • Seizures: rare convulsive events.

Precautions & Warnings

When prescribing Naltrexone, clinicians should consider several safety measures.

  • Liver function assessment: evaluate baseline hepatic enzymes before initiation.
  • Depression monitoring: watch for worsening mood or suicidal thoughts.
  • Acute opioid withdrawal: avoid use during active withdrawal to prevent precipitated symptoms.
  • Concomitant opioid analgesics: do not combine, as analgesic effect will be blocked.
  • Pregnancy and lactation: safety data are limited; use only if clearly needed.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Naltrexone can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Opioid analgesics (e.g., morphine, oxycodone): antagonises analgesic effect and may precipitate withdrawal.
  • Opioid agonist therapy (methadone, buprenorphine): reduces therapeutic benefit and can cause abrupt discontinuation symptoms.
  • Alcohol: may increase risk of hepatotoxicity.

Moderate Interactions (Monitor Closely)

  • CNS depressants (benzodiazepines, barbiturates): additive sedation.
  • Antidepressants (SSRIs, SNRIs): monitor for mood changes.
  • Antihypertensives: possible additive hypotensive effect.

Frequently Asked Questions

Naltrexone "walter Ritter" is indicated for the treatment of alcohol dependence and opioid dependence. It helps reduce cravings and prevents relapse by blocking the rewarding effects of alcohol and opioids.

Naltrexone works by competitively binding to mu‑opioid receptors without activating them. This antagonism blocks the effects of both endogenous opioids and external opioid substances, diminishing their reinforcing properties.

The specific dose and dosing schedule are determined by the prescribing clinician based on the individual’s medical condition, response, and tolerability. Patients should follow the prescriber’s instructions.

Safety data for Naltrexone in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision should be made by a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com specifying 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 an oral opioid antagonist, whereas alternatives like naloxone are administered parenterally for acute overdose. Naltrexone’s longer half‑life makes it suitable for maintenance therapy, while naloxone acts rapidly for emergency reversal.

Store the product below 25 °C in its original packaging, protecting it from moisture and direct sunlight. Do not expose it to extreme temperatures or humidity.

Naltrexone "walter Ritter" is taken orally, usually as a tablet or capsule, with or without food as directed by the prescriber. The exact administration instructions are provided by the healthcare professional.

Serious risks include hepatotoxicity, severe depression, suicidal thoughts, allergic reactions such as rash or angioedema, and rare seizures. Patients should be monitored regularly for these events.

Naltrexone is contraindicated in individuals with acute opioid dependence undergoing withdrawal, those with known hypersensitivity to the drug, and patients with severe hepatic impairment. It should be used with caution in pregnancy, breastfeeding, and in patients with a history of depression.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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