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 severe chronic pain and cancer‑related pain in patients who require long‑term opioid therapy and have tolerance to other opioids. Manufactured in the European Union, the product meets EU pharmacopoeia standards and is distributed under strict regulatory oversight.

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

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Indications & Clinical Uses

Fentanyl is an opioid analgesic used for managing severe pain conditions that require continuous opioid delivery.

  • Severe chronic pain: provides continuous opioid analgesia for patients with high pain intensity and established opioid tolerance.
  • Cancer pain: delivers steady fentanyl levels to alleviate persistent malignant pain in oncology patients.
  • Severe chronic non‑cancer pain: offers long‑acting relief for patients with opioid‑tolerant chronic pain conditions.

How It Works

  • Fentanyl binds as a high‑affinity agonist to μ‑opioid receptors in the central nervous system, activating inhibitory G‑protein pathways that reduce neuronal excitability and diminish the perception of pain. This receptor activation leads to decreased release of neurotransmitters such as substance P and glutamate, resulting in potent analgesic effects while also producing typical opioid‑related central effects.

Side Effects

Fentanyl transdermal therapy may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate feeling of sickness.
  • Constipation: reduced bowel motility leading to hard stools.
  • Drowsiness or fatigue: increased sleepiness during daily activities.
  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Sweating: excessive perspiration unrelated to temperature.
  • Dry mouth: reduced salivation causing oral discomfort.

Serious or Rare Side Effects

  • Respiratory depression: slowed or shallow breathing that can be life‑threatening.
  • Severe hypotension: marked drop in blood pressure causing faintness.
  • Anaphylaxis or severe skin reactions: sudden allergic response with rash, swelling, or difficulty breathing.
  • Opioid dependence or withdrawal: risk of addiction with prolonged use.
  • Adrenal insufficiency: impaired cortisol production leading to fatigue and weakness.

Precautions & Warnings

When prescribing or using Matrifen, careful assessment and monitoring are essential.

  • Assess opioid tolerance: confirm the patient has adequate prior opioid exposure before initiating therapy.
  • Monitor respiratory function: watch for signs of respiratory depression, especially during dose adjustments.
  • Avoid concomitant MAO inhibitors: risk of severe opioid toxicity and hypertensive crisis.
  • Educate on patch disposal: follow local regulations to prevent accidental exposure or misuse.
  • Pregnancy and lactation: use only if the potential benefit justifies the potential risk to the fetus or infant.
  • Store at room temperature: keep in the original pouch, protect from moisture and heat, store below 25°C.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concomitant CNS depressants (e.g., benzodiazepines, barbiturates): may cause profound respiratory depression.
  • Monoamine oxidase inhibitors (MAOIs): increase risk of severe opioid toxicity.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): elevate fentanyl plasma levels and overdose risk.
  • Alcohol: additive central nervous system depression leading to respiratory compromise.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce fentanyl efficacy.
  • Other opioids: cumulative opioid effect can increase sedation and respiratory depression.
  • Anticholinergic agents: may exacerbate constipation, a common opioid side effect.

Frequently Asked Questions

Matrifen is a transdermal patch that contains fentanyl, an opioid analgesic. It is prescribed for the management of severe chronic pain and cancer‑related pain in patients who require continuous, long‑acting opioid therapy and have demonstrated tolerance to other opioid medications.

Fentanyl acts as a high‑affinity agonist at μ‑opioid receptors in the central nervous system. By activating these receptors, it inhibits the release of pain‑transmitting neurotransmitters, reduces neuronal excitability, and produces potent analgesia while also causing typical opioid‑related central effects.

The specific dose and patch strength of Matrifen are determined by the prescribing clinician based on the patient’s pain severity, opioid tolerance, and clinical response. Dosing decisions are individualized and should follow local prescribing guidelines and the product’s prescribing information.

Fentanyl can cross the placenta and be excreted in breast milk. Use during pregnancy or lactation is only recommended when the potential benefit to the mother outweighs the potential risk to the fetus or infant. Clinicians should evaluate each case carefully and discuss alternatives when possible.

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

Matrifen delivers fentanyl via a transdermal system, offering steady plasma concentrations over several days, which can improve adherence compared with multiple daily oral doses. Unlike short‑acting opioids, it provides continuous analgesia but requires careful patient selection for opioid tolerance and monitoring for respiratory depression.

Matrifen patches should be stored at room temperature, below 25 °C, in their original packaging to protect from moisture and heat. Keep the patches away from direct sunlight and do not expose them to extreme temperatures. Follow local regulations for safe disposal after use.

Matrifen is applied to a clean, dry, hair‑free area of the skin, typically on the upper torso or upper arm. The patch adheres for the prescribed duration (usually 72 hours). After removal, the used patch should be folded in half with the adhesive sides together and disposed of according to local hazardous waste guidelines.

The most serious risks include respiratory depression, severe hypotension, and the potential for opioid dependence or withdrawal. Patients should be monitored closely for signs of shallow breathing, low blood pressure, or unusual sedation, especially during dose initiation or when combined with other central nervous system depressants.

Matrifen is contraindicated in patients without established opioid tolerance, those with known hypersensitivity to fentanyl or patch components, individuals taking MAO inhibitors, and patients with significant respiratory compromise, uncontrolled asthma, or severe head injury. Clinicians must assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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