Product image of Metadonhydroklorid Pharmadone (Methadone Hydrochloride) supplied by GNH India

Metadonhydroklorid Pharmadone

Active Ingredient:
Methadone Hydrochloride
Origin:
EU

Metadonhydroklorid Pharmadone (Methadone Hydrochloride)

Methadone Hydrochloride, the active ingredient in Metadonhydroklorid Pharmadone, is a synthetic opioid presented as an oral dosage form for oral use. It is used in the treatment of opioid dependence and chronic pain in adults.

GNH India supplies Metadonhydroklorid Pharmadone as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Unimedic Pharma Ab

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Indications & Clinical Uses

Methadone Hydrochloride is an opioid agonist used in the management of opioid dependence and chronic pain.

  • Opioid dependence: reduces withdrawal symptoms and cravings during maintenance therapy.
  • Chronic pain: provides long‑acting analgesia for severe, persistent pain.
  • Detoxification: facilitates medically supervised opioid withdrawal in controlled settings.

How It Works

  • Methadone Hydrochloride acts as a full agonist at the mu‑opioid receptors in the central nervous system, producing analgesia and suppressing opioid cravings. It also blocks NMDA receptors and inhibits the reuptake of serotonin and norepinephrine, contributing to its efficacy in pain control and withdrawal management.

Side Effects

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

Common Side Effects

  • Constipation: reduced bowel motility leading to hard stools.
  • Drowsiness: increased sleepiness or fatigue.
  • Nausea: feeling of queasiness, sometimes with vomiting.
  • Sweating: excessive perspiration, especially at night.
  • Dry mouth: reduced salivation causing throat discomfort.
  • Weight gain: increased appetite and fluid retention.

Serious or Rare Side Effects

  • Respiratory depression: slowed breathing that can be life‑threatening.
  • QT interval prolongation: cardiac rhythm disturbance that may cause arrhythmia.
  • Seizures: occasional convulsive episodes.
  • Severe hypotension: sudden drop in blood pressure.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Adrenal insufficiency: reduced cortisol production leading to fatigue and weakness.

Precautions & Warnings

Methadone Hydrochloride requires careful monitoring due to its potency and pharmacologic profile.

  • Cardiac assessment: evaluate QT interval before initiating therapy.
  • Respiratory monitoring: watch for signs of respiratory depression, especially during dose changes.
  • Liver function: check hepatic enzymes regularly as metabolism is hepatic.
  • Pregnancy safety: use only if benefits outweigh risks; discuss with obstetric provider.
  • Renal adjustment: consider dose modification in severe renal impairment.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Methadone Hydrochloride interacts with several drug classes; some combinations should be avoided while others need close monitoring.

Major Interactions (Avoid)

  • Benzodiazepines: additive CNS depression and increased risk of respiratory failure.
  • MAO inhibitors: risk of severe hypotension and serotonin syndrome.
  • QT‑prolonging agents: heightened chance of cardiac arrhythmias.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): may lower methadone plasma levels.
  • CYP3A4 inhibitors (e.g., erythromycin): may raise methadone concentrations.
  • Antidepressants (SSRIs, SNRIs): potential for serotonin syndrome.
  • Anticholinergics: may exacerbate constipation.
  • NSAIDs: increased risk of gastrointestinal bleeding.

Frequently Asked Questions

Metadonhydroklorid Pharmadone contains methadone hydrochloride and is prescribed for opioid dependence treatment and for managing chronic, severe pain. It helps reduce withdrawal symptoms in people with opioid use disorder and provides long‑acting analgesia for persistent pain conditions.

Methadone hydrochloride is a full agonist at mu‑opioid receptors, which suppresses pain signals and diminishes cravings for other opioids. It also blocks NMDA receptors and inhibits reuptake of serotonin and norepinephrine, contributing to its effectiveness in both analgesia and withdrawal management.

The dose of methadone is individualized. A qualified prescriber determines the appropriate starting dose and any subsequent adjustments based on the patient’s clinical condition, prior opioid exposure, and response to therapy. Dosing information is provided on the prescription label.

Methadone can be used during pregnancy when the benefits outweigh potential risks, as abrupt withdrawal may harm both mother and fetus. Breastfeeding is generally permitted if the mother is on a stable dose, but infants should be monitored for signs of sedation or respiratory depression.

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 (including any cold‑chain requirements) and necessary import documentation.

Both methadone and buprenorphine are opioid agonists used for maintenance therapy, but methadone is a full agonist offering stronger analgesia, while buprenorphine is a partial agonist with a ceiling effect that reduces overdose risk. Choice depends on patient history, treatment goals, and clinician assessment.

Store Metadonhydroklorid Pharmadone at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, direct sunlight, and extreme temperature fluctuations to maintain potency.

Metadonhydroklorid Pharmadone is taken orally, usually as a tablet or liquid formulation, according to the prescriber’s instructions. It should be swallowed whole with water and taken at the same time each day to maintain stable blood levels.

The most serious risks include respiratory depression, especially when combined with other CNS depressants, and cardiac arrhythmias due to QT interval prolongation. Patients should be monitored for signs of overdose, severe drowsiness, or irregular heartbeats, and any concerning symptoms should prompt immediate medical attention.

Methadone is contraindicated in individuals with known hypersensitivity to methadone or any of its excipients, those with severe respiratory depression, uncontrolled asthma, or significant cardiac conduction abnormalities. Caution is also advised for patients with severe liver disease, as metabolism may be impaired.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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