Product image of Matrifen (Fentanyl) supplied by GNH India

Matrifen

Active Ingredient:
Fentanyl
Origin:
EU

Matrifen (Fentanyl)

Fentanyl, the active ingredient in Matrifen, is an opioid analgesic presented as a transdermal patch for transdermal use. It provides continuous systemic delivery of fentanyl to manage chronic cancer pain and severe chronic non‑cancer pain in patients who require around‑the‑clock opioid therapy.

GNH India supplies Matrifen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU quality standards and offers regulatory‑supported sourcing for global markets.

Manufacturer / TM Owner

Istituto Gentili S.R.L

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Indications & Clinical Uses

Fentanyl transdermal patches are used to provide opioid analgesia for persistent pain conditions.

  • Chronic cancer pain: delivers continuous opioid relief for patients with ongoing malignant pain.
  • Severe chronic non‑cancer pain: supplies steady fentanyl levels for opioid‑tolerant individuals with debilitating non‑cancer pain.
  • Opioid‑tolerant patients requiring long‑term analgesia: offers a convenient, non‑oral delivery system for continuous pain control.

How It Works

  • Fentanyl binds to μ‑opioid receptors in the central nervous system, activating inhibitory G‑protein pathways that reduce neuronal excitability and diminish the transmission of nociceptive signals. This receptor agonism leads to potent analgesia by decreasing the perception of pain and altering pain‑modulating pathways.

Side Effects

Fentanyl patches can cause a range of adverse reactions, from mild to life‑threatening.

Common Side Effects

  • Nausea: feeling of sickness or urge to vomit.
  • Constipation: reduced bowel movements and hard stools.
  • Drowsiness: increased sleepiness or fatigue.
  • Dry mouth: reduced salivation leading to a parched feeling.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be fatal.
  • Severe hypotension: marked drop in blood pressure causing dizziness or fainting.
  • Skin necrosis at the application site: tissue death requiring medical attention.
  • Anaphylaxis: severe allergic reaction with rash, swelling, and airway compromise.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient suitability and implement safety measures.

  • Assess opioid tolerance: confirm the patient is opioid‑tolerant before starting a fentanyl patch.
  • Monitor respiratory function: watch for signs of respiratory depression, especially after dose adjustments.
  • Avoid concurrent CNS depressants: limit use of benzodiazepines, alcohol, or other sedatives.
  • Use the lowest effective dose: titrate to achieve pain control while minimizing side effects.
  • Educate patient on patch disposal: fold used patch and discard according to local regulations.
  • Store at room temperature: keep in the original pouch, protect from moisture and heat, and store away from direct sunlight.

Avoid Interactions

Fentanyl may interact with other medicines, altering its safety or effectiveness.

Major Interactions (Avoid)

  • Benzodiazepines or other CNS depressants: can cause profound respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): increase risk of severe hypotension and serotonin syndrome.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): raise fentanyl plasma levels, heightening toxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce fentanyl concentrations, decreasing analgesia.
  • Other opioids: additive sedation and respiratory effects require careful dosing.
  • Alcohol and antihistamines: can enhance central nervous system depression and should be used with caution.

Frequently Asked Questions

Matrifen is a fentanyl transdermal patch indicated for the management of chronic cancer pain and severe chronic non‑cancer pain in patients who are opioid‑tolerant and need continuous, around‑the‑clock analgesia.

Fentanyl in Matrifen is absorbed through the skin and binds to μ‑opioid receptors in the central nervous system. This binding activates inhibitory pathways that reduce neuronal excitability and block the transmission of pain signals, providing potent analgesic effects.

The specific dose of Matrifen is determined by the prescribing clinician based on the patient’s opioid tolerance, pain severity, and clinical response. The prescriber selects the appropriate patch strength and replacement interval.

The safety of fentanyl patches in pregnancy and lactation has not been established. They are generally avoided unless the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To request Matrifen, 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.

Matrifen delivers fentanyl continuously via a transdermal system, offering more stable plasma levels than oral opioids that require multiple daily doses. This can improve adherence and reduce peaks and troughs in pain control, but it also requires careful patient selection and monitoring for respiratory depression.

Matrifen patches should be stored at room temperature, below 25 °C, in their original packaging. Keep them away from moisture, direct heat, and sunlight. Do not expose the patches to extreme temperatures or crush them, as this may affect drug delivery.

Matrifen is applied to a clean, dry, hair‑free area of the skin, usually on the upper torso or upper arm. The patch is pressed firmly for about 30 seconds to ensure adhesion and is typically replaced every 72 hours, following the prescriber’s instructions.

The most serious risks include respiratory depression, severe hypotension, and potential for overdose, especially if used with other central nervous system depressants. Patients should be monitored closely for signs of shallow breathing, low blood pressure, or excessive sedation.

Matrifen should not be used in patients who are not opioid‑tolerant, have severe respiratory insufficiency, uncontrolled asthma, or known hypersensitivity to fentanyl or patch components. It is also contraindicated in patients taking MAO inhibitors within 14 days of starting therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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