MedPath
HSA Product

PECFENT NASAL SPRAY SOLUTION 100 MCG/SPRAY

Product approved by Health Sciences Authority (SG)

Basic Information

PECFENT NASAL SPRAY SOLUTION 100 MCG/SPRAY

SPRAY, METERED

Regulatory Information

SIN16026P

October 12, 2020

Prescription Only

Therapeutic

NASAL

August 10, 2023

June 3, 2025

XN02AB03

Company Information

A. MENARINI SINGAPORE PTE. LTD.

A. MENARINI SINGAPORE PTE. LTD.

Active Ingredients

FENTANYL CITRATE eqv. FENTANYL

Strength: 100 μg/spray

Detailed Information

Contraindications

**4.3 Contraindications** Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_. Patients without maintenance opioid therapy as there is an increased risk of respiratory depression. Severe respiratory depression or severe obstructive lung conditions. Treatment of acute pain other than breakthrough pain. Patients being treated with medicinal products containing sodium oxybate.

Indication Information

**4.1 Therapeutic indications** PecFent is indicated for the management of breakthrough pain (BTP) in adults who are already receiving maintenance opioid therapy for chronic cancer pain. Breakthrough pain is a transitory exacerbation of pain that occurs on a background of otherwise controlled persistent pain. Patients receiving maintenance opioid therapy are those who are taking at least 60 mg of oral morphine daily, at least 25 micrograms of transdermal fentanyl per hour, at least 30 mg of oxycodone daily, at least 8 mg of oral hydromorphone daily or an equianalgesic dose of another opioid for a week or longer.

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