MedPath
HSA Product

FERRIPROX FILM-COATED TABLET 500 mg

Product approved by Health Sciences Authority (SG)

Basic Information

FERRIPROX FILM-COATED TABLET 500 mg

TABLET, FILM COATED

Regulatory Information

SIN12083P

September 25, 2002

Prescription Only

Therapeutic

ORAL

August 10, 2023

June 4, 2025

XV03AC02

Company Information

APOTEX INC

PHARMAFORTE SINGAPORE PTE LTD

PHARMAFORTE SINGAPORE PTE LTD

Active Ingredients

Deferiprone

Strength: 500mg

Detailed Information

Contraindications

**4.3 Contraindications** - Hypersensitivity to the active substance or to any of the excipients. - History of recurrent episodes of neutropenia. - History of agranulocytosis. - Pregnancy or breast-feeding (see section 4.6 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). - Due to the unknown mechanism of deferiprone-induced neutropenia, patients must not take medicinal products known to be associated with neutropenia or those that can cause agranulocytosis (see section 4.5 – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).

Indication Information

**4.1 Therapeutic indications** Ferriprox® is indicated for the treatment of iron overload in patients with thalassaemia major when deferoxamine therapy is contraindicated or inadequate.

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