Product image of Matrifen (Fentanyl) supplied by GNH India

Matrifen

Active Ingredient:
Fentanyl
Origin:
EU

Matrifen (Fentanyl)

Fentanyl, the active ingredient in Matrifen, is a opioid analgesic presented as a transdermal patch for transdermal use. It treats severe chronic pain and cancer pain in patients requiring continuous opioid therapy.

GNH India supplies Matrifen as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Istituto Gentili S.R.L

1
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Indications & Clinical Uses

Matrifen (fentanyl) is used in the management of pain conditions that require strong opioid therapy.

  • Severe chronic non‑cancer pain: provides continuous analgesia for patients with long‑term pain unresponsive to weaker opioids.
  • Cancer‑related pain: delivers steady opioid levels to control moderate to severe pain in oncology patients.
  • End‑of‑life pain management: ensures consistent pain relief for patients in palliative care settings.

How It Works

  • Fentanyl binds with high affinity to mu‑opioid receptors in the central nervous system, activating inhibitory G‑protein pathways that reduce neuronal excitability and diminish the perception of pain. When delivered through a transdermal patch, the drug is absorbed slowly into systemic circulation, maintaining stable plasma concentrations over several days.

Side Effects

Fentanyl transdermal therapy may be associated with a range of adverse reactions, which are grouped by frequency and severity.

Common Side Effects

  • Nausea: feeling of sickness or urge to vomit.
  • Constipation: reduced bowel movements and hard stools.
  • Dizziness: light‑headedness or unsteady sensation.
  • Somnolence: increased sleepiness or fatigue.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing dizziness or fainting.
  • Opioid dependence or withdrawal: risk of addiction and withdrawal symptoms upon abrupt discontinuation.

Precautions & Warnings

When prescribing Matrifen, clinicians should observe several safety measures to minimize risk.

  • Assess opioid tolerance: confirm patient has prior exposure to strong opioids before initiating therapy.
  • Evaluate respiratory function: perform baseline assessment and monitor for depression.
  • Monitor for signs of addiction: watch for drug‑seeking behavior and dependence.
  • Adjust dose in hepatic impairment: reduce dosage or extend interval in patients with liver dysfunction.
  • Use with caution in elderly: start at the lowest effective dose and observe closely.
  • Store at room temperature: keep patch in original packaging, protect from moisture and light.

Avoid Interactions

Fentanyl may interact with other medicines, altering its effect or increasing adverse reactions.

Major Interactions (Avoid)

  • Central nervous system depressants (e.g., benzodiazepines): can cause profound sedation and respiratory depression.
  • Monoamine oxidase inhibitors: increase risk of serotonin syndrome and severe hypotension.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): raise fentanyl plasma levels and risk of toxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): may reduce fentanyl effectiveness.
  • Diuretics: can enhance hypotensive effects when combined with fentanyl.

Frequently Asked Questions

Matrifen is a transdermal fentanyl patch indicated for the management of severe chronic pain, including cancer‑related pain and end‑of‑life pain, in patients who require continuous opioid therapy and have demonstrated tolerance to strong opioids.

Fentanyl exerts its analgesic effect by binding to mu‑opioid receptors in the brain and spinal cord, activating inhibitory G‑protein pathways that decrease neuronal firing and block the transmission of pain signals, resulting in reduced perception of pain.

The appropriate 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 patch strength and replacement interval that best matches the individual’s therapeutic needs.

Safety of fentanyl patches in pregnancy or lactation has not been established. Use is generally avoided unless the potential benefit justifies the potential risk to the fetus or infant, and it should be discussed with 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.

Compared with oral opioids, the transdermal fentanyl patch provides steady plasma concentrations over several days, reducing the need for multiple daily dosing. It is generally reserved for patients who need continuous, long‑term opioid therapy and have adequate opioid tolerance, whereas weaker opioids may be used for intermittent pain.

Matrifen patches should be stored at room temperature, below 25 °C, in their original foil pouch, protected from moisture, heat and direct light. Do not expose the patches to temperatures above the recommended range, as this may affect drug stability.

The patch is applied to a clean, dry, hair‑free area of the upper torso or upper arm. After removing the backing, press the adhesive side firmly for at least 30 seconds, then replace the patch at the prescribed interval, usually every 72 hours, following the prescriber’s instructions.

The most critical risks include respiratory depression, severe hypotension, and the potential for opioid dependence or withdrawal. Patients should be monitored closely for signs of slowed breathing, low blood pressure, or abnormal behavior, and the patch should be removed immediately if serious adverse effects occur.

Matrifen is contraindicated in patients who are opioid‑naïve, have significant respiratory compromise, uncontrolled severe asthma, known hypersensitivity to fentanyl or patch components, or who are taking MAO‑inhibitors. It should also be avoided in individuals with severe hepatic impairment unless dose adjustments are made.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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