Product image of L-Polaflux (Levomethadone Hydrochloride) supplied by GNH India

L-Polaflux

Active Ingredient:
Levomethadone Hydrochloride
Origin:
EU

L-Polaflux (Levomethadone Hydrochloride)

Levomethadone Hydrochloride, the active ingredient in L-Polaflux, is an opioid analgesic presented as an oral formulation for oral use. It is employed in the management of opioid dependence and chronic pain in adult patients, providing withdrawal symptom control and analgesia.

GNH India supplies L-Polaflux as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality‑assured product availability across global markets. The company adheres to EU GMP standards and provides comprehensive logistics support for timely delivery to its clients.

Manufacturer / TM Owner

Hexal Ag

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Indications & Clinical Uses

Levomethadone Hydrochloride is used in opioid‑related disorders and pain management, acting on the central opioid system.

  • Opioid dependence: helps reduce withdrawal symptoms and supports maintenance therapy in patients undergoing opioid substitution.
  • Chronic pain: provides analgesic effect for persistent moderate to severe pain when other treatments are insufficient.
  • Opioid withdrawal management: facilitates safe tapering by alleviating acute withdrawal signs during detoxification programs.

How It Works

  • Levomethadone Hydrochloride is the levorotatory isomer of methadone that acts as a full agonist at the μ‑opioid receptor. By binding to this receptor, it mimics endogenous opioids, producing analgesia and suppressing the neuronal pathways responsible for withdrawal. The drug also exhibits NMDA receptor antagonism, which may contribute to its efficacy in chronic pain and reduces tolerance development.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Constipation: reduced bowel movements.
  • Drowsiness: increased sleepiness or fatigue.
  • Dizziness: light‑headed sensation.
  • Sweating: excessive perspiration.
  • Dry mouth: reduced salivation.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing, potentially life‑threatening.
  • Cardiac arrhythmia: abnormal heart rhythm, including QT prolongation.
  • Seizures: convulsive episodes.
  • Severe hypotension: marked drop in blood pressure.
  • Allergic reactions: rash, itching, swelling, or anaphylaxis.

Precautions & Warnings

When prescribing Levomethadone Hydrochloride, clinicians should observe several safety precautions.

  • Assess patient history: evaluate prior opioid use, dependence risk, and respiratory conditions.
  • Monitor cardiac function: baseline ECG and periodic QT interval checks are recommended.
  • Adjust dose in renal/hepatic impairment: reduce dosage for patients with compromised liver or kidney function.
  • Avoid concurrent CNS depressants: limit use with benzodiazepines, alcohol, or other sedatives.
  • Counsel on driving: advise patients about possible drowsiness and impaired coordination.
  • Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and light.

Avoid Interactions

Levomethadone Hydrochloride interacts with several medicines; awareness of these interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Other opioid agonists: additive respiratory depression and sedation.
  • QT‑prolonging agents: increased risk of cardiac arrhythmia (e.g., certain antiarrhythmics, macrolide antibiotics).
  • CNS depressants: heightened sedation and respiratory compromise (e.g., benzodiazepines, barbiturates).

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors: may raise levomethadone levels (e.g., ketoconazole, erythromycin).
  • CYP3A4 inducers: may reduce drug exposure (e.g., rifampin, carbamazepine).
  • Antidepressants: potential for serotonin syndrome when combined with serotonergic agents.

Frequently Asked Questions

L-Polaflux contains levomethadone hydrochloride and is indicated for the treatment of opioid dependence, management of chronic pain, and assistance in opioid withdrawal programs. It helps stabilize patients undergoing substitution therapy and provides analgesia for persistent moderate to severe pain.

Levomethadone Hydrochloride is a full agonist at the μ‑opioid receptor. By binding to this receptor, it mimics endogenous opioids, producing analgesic effects and suppressing the neuronal pathways that generate withdrawal symptoms. Its additional NMDA‑receptor antagonism may enhance pain control and reduce tolerance.

The dosage of L-Polaflux is individualized. A qualified prescriber determines the appropriate dose based on the patient’s clinical condition, prior opioid exposure, and response to therapy. No fixed regimen is provided in public literature.

Safety data for levomethadone hydrochloride in pregnancy and lactation are limited. The product is classified as having an unknown pregnancy category, and clinicians should weigh potential benefits against risks. Breastfeeding mothers should consult a healthcare professional before use.

To order L-Polaflux, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

L-Polaflux contains the levorotatory isomer of methadone, which generally offers a more favorable safety profile with reduced cardiotoxicity compared with racemic methadone. Both act as μ‑opioid agonists, but levomethadone may require lower doses to achieve equivalent analgesic or substitution effects.

L-Polaflux should be stored at ambient temperature, preferably below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme heat. Keep out of reach of children and handle according to standard pharmaceutical safety procedures.

L-Polaflux is administered orally. The tablet or capsule is swallowed whole with water, unless otherwise directed by a healthcare professional. It should be taken exactly as prescribed, and patients should not alter the route of administration.

The most serious risks include respiratory depression, which can be life‑threatening, and cardiac arrhythmias such as QT‑interval prolongation. Patients should be monitored for signs of shallow breathing, severe dizziness, or irregular heartbeats, especially when initiating therapy or adjusting doses.

L-Polaflux is contraindicated in individuals with known hypersensitivity to levomethadone or any component of the formulation, in patients with severe respiratory depression, uncontrolled asthma, or significant cardiac conduction disorders. Caution is also advised for those taking other CNS depressants.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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