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 treats severe chronic pain, cancer‑related pain and breakthrough pain in patients who need 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
Pack/s
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Indications & Clinical Uses

Fentanyl, an opioid analgesic, is indicated for conditions that require sustained opioid delivery.

  • Severe chronic non‑cancer pain: provides continuous analgesia over several days.
  • Cancer‑related pain: maintains steady plasma levels for tumor‑associated pain.
  • Breakthrough pain management: used together with short‑acting opioids to control episodic pain spikes.

How It Works

  • Fentanyl binds selectively to μ‑opioid receptors in the central nervous system, activating inhibitory G‑protein pathways that reduce neuronal excitability and decrease the release of excitatory neurotransmitters. This action lowers the perception of pain and produces analgesia while also affecting respiratory drive and gastrointestinal motility.

Side Effects

Fentanyl transdermal therapy can be associated with a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate upset stomach.
  • Constipation: reduced bowel movements.
  • Somnolence: increased sleepiness.
  • Dizziness: feeling light‑headed.
  • Application site erythema: redness where the patch is placed.
  • Pruritus: itching at the patch site.

Serious or Rare Side Effects

  • Respiratory depression: dangerously slow breathing.
  • Severe hypotension: marked drop in blood pressure.
  • Cardiac arrhythmia: irregular heart rhythm.
  • Adrenal insufficiency: inadequate cortisol production.
  • Severe skin reactions: Stevens‑Johnson syndrome or necrosis.
  • Opioid dependence or withdrawal syndrome upon abrupt discontinuation.

Precautions & Warnings

When prescribing or dispensing Matrifen, several safety measures should be observed.

  • Assess opioid tolerance: confirm the patient is opioid‑experienced before initiating therapy.
  • Rotate application site: change the skin area with each new patch to avoid irritation.
  • Monitor respiratory function: especially during the first 24 hours and after dose adjustments.
  • Avoid concurrent MAO inhibitors: risk of severe hypertension or serotonin syndrome.
  • Educate on disposal: used patches must be folded and placed in a sharps container.
  • Store at room temperature: keep in the original pouch, protect from moisture and direct heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Other strong opioids: additive respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Central nervous system depressants (e.g., benzodiazepines): profound sedation and respiratory compromise.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): increase fentanyl plasma levels.
  • Alcohol: enhances sedative effects and respiratory depression.
  • CYP3A4 inducers (e.g., rifampin, St. John’s wort): may reduce analgesic efficacy.

Frequently Asked Questions

Matrifen is a fentanyl transdermal patch indicated for the management of severe chronic pain, cancer‑related pain, and breakthrough pain that requires continuous opioid delivery. It provides steady plasma concentrations over several days, reducing the need for frequent dosing.

Fentanyl is a μ‑opioid receptor agonist. By binding to these receptors in the brain and spinal cord, it activates inhibitory pathways that lower neuronal excitability, diminish the release of pain‑transmitting neurotransmitters, and produce potent analgesia.

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 is not well established. Because fentanyl can cross the placenta and enter breast milk, it should be used only if the potential benefit justifies the potential risk to the fetus or infant.

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 through the skin, offering more stable plasma levels than oral or injectable opioids that require multiple daily doses. This can improve pain control and reduce peaks and troughs, but it also demands careful monitoring for respiratory depression and proper disposal of used patches.

Matrifen patches should be stored at room temperature, below 25 °C, in their original packaging. Keep them away from moisture, direct sunlight and heat sources to maintain patch integrity and drug potency.

The patch is applied to clean, dry, hair‑free skin on the upper torso, upper arm, or thigh. Press firmly for about 30 seconds, then cover with a protective dressing if needed. Patches are typically replaced every 72 hours, following the prescriber’s schedule.

The most serious risks include respiratory depression, severe hypotension, cardiac arrhythmias, and opioid dependence. Patients should be educated to recognize signs of shallow breathing, extreme drowsiness, or fainting and to seek immediate medical attention if they occur.

Matrifen is contraindicated in patients who are opioid‑naïve, have severe respiratory insufficiency, uncontrolled asthma, known hypersensitivity to fentanyl or patch components, or who are taking MAO inhibitors within 14 days. It should also be avoided in individuals with significant hepatic impairment without specialist supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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