Product image of Metadon Dak (Methadone Hydrochloride) supplied by GNH India

Metadon Dak

Active Ingredient:
Methadone Hydrochloride
Origin:
EU

Metadon Dak (Methadone Hydrochloride)

Methadone Hydrochloride, the active ingredient in Metadon Dak, is an opioid presented as an oral dosage form for oral use. It provides long‑acting analgesia and suppresses withdrawal symptoms, making it suitable for opioid dependence treatment and for managing severe chronic pain in adult patients requiring continuous opioid therapy.

GNH India supplies Metadon Dak as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance across global markets. The company adheres to stringent manufacturing standards and provides reliable logistics support for timely delivery.

Manufacturer / TM Owner

Orifarm Healthcare A/S

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Indications & Clinical Uses

Methadone, an opioid agonist, is used in the management of conditions that involve opioid pathways, particularly where long‑acting therapy is required.

  • Opioid dependence treatment: reduces withdrawal symptoms and supports maintenance therapy to help patients achieve abstinence.
  • Severe chronic pain: provides long‑acting analgesia for patients who need continuous opioid control.
  • Opioid detoxification: facilitates safe transition from short‑acting opioids during supervised withdrawal programs.

How It Works

  • Methadone acts as a full agonist at the μ‑opioid receptor, binding with high affinity and activating the receptor to produce analgesia and suppress central nervous system manifestations of opioid withdrawal. By stabilizing receptor activity, it reduces the surge of neurotransmitters associated with pain and dependence, while its long half‑life provides sustained effect with once‑daily dosing in many patients.

Side Effects

Methadone may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Constipation: reduced gastrointestinal motility leading to hard stools.
  • Nausea: feeling of queasiness often occurring after dosing.
  • Drowsiness: increased sleepiness or fatigue.
  • Dry mouth: reduced salivation causing throat discomfort.

Serious or Rare Side Effects

  • Respiratory depression: slowed breathing that can be life‑threatening.
  • QT interval prolongation: cardiac electrical disturbance that may cause arrhythmia.
  • Severe hypotension: marked drop in blood pressure leading to dizziness or fainting.
  • Anaphylactic reaction: sudden severe allergic response requiring emergency care.

Precautions & Warnings

When prescribing methadone, several precautions should be observed to minimize risk.

  • Assess respiratory function: evaluate baseline breathing and monitor for depression, especially during dose initiation.
  • Monitor cardiac status: obtain ECG to check QT interval and avoid use with other QT‑prolonging agents.
  • Use caution in hepatic impairment: adjust dosing and observe for accumulation due to reduced metabolism.
  • Avoid abrupt discontinuation: taper gradually to prevent precipitated withdrawal symptoms.
  • Evaluate for concurrent CNS depressants: limit use with benzodiazepines or alcohol to reduce respiratory risk.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Methadone interacts with several medicines; awareness of these interactions helps prevent adverse events.

Major Interactions (Avoid)

  • Concomitant CNS depressants (e.g., benzodiazepines, barbiturates): may cause profound respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): increase risk of serotonin syndrome and hypertensive crisis.
  • QT‑prolonging drugs (e.g., quinidine, sotalol): additive effect on cardiac repolarization.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may lower methadone concentrations, reducing efficacy.
  • Selective serotonin reuptake inhibitors (e.g., fluoxetine, sertraline): can modestly increase methadone levels.
  • Alcohol: additive CNS depression, requires caution.

Frequently Asked Questions

Metadon Dak contains methadone hydrochloride and is prescribed for the treatment of opioid dependence, helping to suppress withdrawal symptoms, as well as for the management of severe chronic pain where long‑acting opioid therapy is required.

Methadone is a full agonist at the μ‑opioid receptor. By binding to this receptor it activates the same pathways as endogenous opioids, producing analgesia and reducing the neuro‑chemical disturbances that cause withdrawal in dependent individuals.

The appropriate dose of Metadon Dak is individualized by the prescribing clinician based on the patient’s medical condition, prior opioid exposure, renal and hepatic function, and response to therapy. No fixed dosing regimen is provided here.

Data on methadone use in pregnancy and lactation are limited. It may be prescribed when the benefits outweigh potential risks, but clinicians should evaluate each case carefully and monitor both mother and infant for adverse effects.

To request Metadon Dak, 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.

Both methadone and buprenorphine are used for opioid dependence, but methadone is a full μ‑opioid agonist offering stronger analgesia, while buprenorphine is a partial agonist with a ceiling effect on respiratory depression, often considered to have a lower overdose risk.

Metadon Dak should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperatures to maintain potency and stability.

Metadon Dak is taken orally, usually as a tablet or liquid formulation, as directed by the prescriber. Doses are typically administered once daily, but the exact schedule depends on the individual treatment plan.

The most critical risks include respiratory depression, which can be life‑threatening, QT interval prolongation that may lead to cardiac arrhythmias, severe hypotension, and rare but severe allergic reactions such as anaphylaxis.

Methadone is contraindicated in patients with known hypersensitivity to methadone, those taking monoamine oxidase inhibitors, individuals with uncontrolled severe respiratory disease, and patients with significant QT prolongation without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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