BeneFIX | European Medicines Agency (EMA)

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Overview

This is a summary of the European Public Assessment Report (EPAR) for BeneFIX. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for BeneFIX.

BeneFIX is a medicine that contains the active substance nonacog alfa. It is available as a powder and solvent that are mixed together to form a solution for injection.

BeneFIX is used for the treatment and prevention of bleeding in adults and children with haemophilia B (an inherited bleeding disorder). BeneFIX is intended for either short-term or long-term use.

The medicine can only be obtained with a prescription.

BeneFIX should be started by a doctor who has experience in the treatment of haemophilia. During treatment, the doctor should regularly carry out blood tests to adjust the dose to be given.

BeneFIX is given by a slow injection into a vein, usually at up to 4 ml per minute and should not be mixed with other infusion solutions or given using a kit other than the one supplied with the medicine. The dose and the frequency of injection depend on whether BeneFIX is used to treat or prevent bleeding, or to reduce bleeding during surgery, and on the patient’s condition. The dose is adjusted depending on the severity and location of the bleeding, or the type of surgery. Full details on how to calculate the dose are included in the summary of product characteristics.

Patients or their carers can give injections of BeneFIX, provided that they have been trained appropriately.

The active substance in BeneFIX, nonacog alfa, is a blood coagulation factor protein (a substance that helps the blood to clot). Patients with haemophilia B lack a protein called factor IX, which is involved in blood clotting. The lack of factor IX causes blood-clotting problems, such as bleeding in the joints, muscles and internal organs. BeneFIX is used to replace the missing factor IX. It corrects the factor IX deficiency and gives temporary control of the bleeding disorder.

Nonacog alfa is not extracted from human blood but produced by a method known as ‘recombinant DNA technology’: it is made by cells that have received a gene (DNA), which makes them able to produce human coagulation factor IX.

BeneFIX has been studied in previously treated patients with moderate or severe haemophilia B for prevention or to treat bleeding episodes during and after surgery. It has also been studied in patients who have not received any treatment for their haemophilia. The studies assessed the number of bleeding episodes that occurred and rated BeneFIX’s effectiveness using a scale from ‘no response’ to ‘excellent’.

In previously treated patients, 82% of the 693 bleeding episodes treated resolved after a single infusion of BeneFIX. Out of 972 infusions, 84% were rated as bringing about ‘good’ or ‘excellent’ responses.

Hypersensitivity (allergic) reactions have been seen in patients treated with products containing factor IX and may sometimes be severe. They include angioedema (swelling of the face and limbs), burning and stinging at the injection site, chills, flushing, urticaria (itchy rash), headache, hives, hypotension (low blood pressure), lethargy, nausea (feeling sick), restlessness, tachycardia (fast heartbeat), tightness of the chest, tingling, vomiting and wheezing. Patients with haemophilia B may also develop neutralising antibodies (inhibitors) to factor IX. If antibodies develop, BeneFIX will not work effectively, which may result in a loss of bleeding control. For the full list of all side effects reported with BeneFIX, see the package leaflet.

BeneFIX must not be used in people who are hypersensitive (allergic) to recombinant coagulation factor IX, to any of the other ingredients, or to hamster proteins.

The CHMP decided that BeneFIX’s benefits are greater than its risks and recommended that it be given marketing authorisation.

A risk management plan has been developed to ensure that BeneFIX is used as safely as possible. Based on this plan, safety information has been included in the summary of product characteristics and the package leaflet for BeneFIX, including the appropriate precautions to be followed by healthcare professionals and patients.

The European Commission granted a marketing authorisation valid throughout the European Union for BeneFIX on 27 August 1997.

For more information about treatment with BeneFIX, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

English (EN)
(83.05 KB – PDF)

First published: 12/05/2009Last updated: 30/10/2015

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English (EN)
(177.73 KB – PDF)

First published: 14/05/2020

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Product information

English (EN)
(498.35 KB – PDF)

First published: 26/11/2009Last updated: 07/03/2025

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Latest procedure affecting product information:
N/0000252321

06/03/2025

This medicine’s product information is available in all official EU languages.
Select ‘available languages’ to access the language you need.

Product information documents contain:

summary of product characteristics (annex I);
manufacturing authorisation holder responsible for batch release (annex IIA);
conditions of the marketing authorisation (annex IIB);
labelling (annex IIIA);
package leaflet (annex IIIB).

English (EN)
(27.17 KB – PDF)

First published: 06/06/2008Last updated: 30/03/2017

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Product details

Name of medicine: BeneFIX
Active substance: Nonacog alfa
International non-proprietary name (INN) or common name: nonacog alfa
Therapeutic area (MeSH): Hemophilia B
Anatomical therapeutic chemical (ATC) code: B02BD04

Pharmacotherapeutic group

Antihemorrhagics

Therapeutic indication

Treatment and prophylaxis of bleeding in patients with haemophilia B (congenital factor-IX deficiency).

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