Land: Irland
Språk: engelska
Källa: HPRA (Health Products Regulatory Authority)
Feiba
Baxalta Innovations GmbH
B02BD; B02BD03
Feiba
50 unit(s)/millilitre
Powder and solvent for solution for infusion
slow infusion via the intravenous route
1 vial with 1000 U FEIBA powder for solution for infusion or 1 vial with 2500 U FEIBA powder for solution for infusion
Product subject to prescription which may not be renewed (A)
blood coagulation factors
Blood coagulation factors; factor VIII inhibitor bypassing activity
It is used for: treatment of bleeding in hemophilia A patients with inhibitors; treatment of bleeding in hemophilia B patients with inhibitors, if no other specific treatment is available (see section 5.1); treatment of bleeding in non-hemophiliacs with acquired inhibitors to factor VIII; prophylaxis of bleeding in hemophilia A patients with inhibitors who have experienced a significant bleed or are at high risk of significant bleeding
Marketed
2010-05-28
1 PACKAGE LEAFLET: INFORMATION FOR THE USER FEIBA 50 U/ML POWDER AND SOLVENT FOR SOLUTION FOR INFUSION ACTIVE SUBSTANCE: Factor VIII Inhibitor Bypassing Activity READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START USING THIS MEDICINE BECAUSE IT CONTAINS IMPORTANT INFORMATION FOR YOU. - Keep this leaflet. You may need to read it again. - If you have any further questions, please ask your doctor or pharmacist. - This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours. - If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. IN THIS LEAFLET: 1. What FEIBA 50 U/ml is and what it is used for. 2. What you need to know before you use FEIBA 50 U/ml. 3. How to use FEIBA 50 U/ml. 4. Possible side effects. 5. How to store FEIBA 50 U/ml. 6. Content of the pack and other information. 1. WHAT FEIBA 50 U/ML IS AND WHAT IT IS USED FOR FEIBA is a preparation made from human plasma which allows hemostasis, even when individual coagulation factors are reduced or absent. FEIBA is used for the treatment of bleedings in inhibitor haemophilia A patients. FEIBA is used for the treatment of bleedings in inhibitor haemophilia B patients, if no other specific treatment is available. FEIBA is also used for prophylaxis of bleeding in inhibitor haemophilia A patients who have experienced a _ _ significant bleed or are at high risk of significant bleeding. Furthermore, FEIBA may be used for the treatment of bleedings in non-haemophilic patients who have acquired inhibitors to factor VIII. 2 2. WHAT YOU NEED TO KNOW BEFORE YOU USE FEIBA 50 U/ML. Please inform your doctor if you have a known allergy. Please inform your doctor if you are on a low-sodium diet. DO NOT USE FEIBA In the following situations FEIBA should only be used if - for example due to a very high inhibitor titre - no response to treatment with the appropriate coagulation factor concentrate can be expected. if you are Läs hela dokumentet
Health Products Regulatory Authority 02 December 2020 CRN00C00H Page 1 of 13 SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT FEIBA 50 U/ml powder and solvent for solution for infusion 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Active substance: Factor VIII Inhibitor Bypassing Activity 1 ml contains 50 U* factor VIII inhibitor bypassing activity. FEIBA 50 U/ml is available in three different presentations: The presentation 500 U FEIBA contains 500 U factor VIII inhibitor bypassing activity in 200 – 600 mg human plasma protein The presentation 1000 U FEIBA contains 1000 U factor VIII inhibitor bypassing activity in 400 – 1,200 mg human plasma protein. The presentation 2500 U FEIBA contains 2500 U factor VIII inhibitor bypassing activity in 1,000 – 3,000 mg human plasma protein. FEIBA also contains the factors II, IX and X, mainly in non-activated form, as well as activated factor VII. Factor VIII coagulation antigen (F VIII C:Ag) is present at a concentration of up to 0.1 U./1 U. FEIBA. The factors of the kallikrein-kinin system are present in trace amounts only, if at all. * 1 unit of FEIBA shortens the activated partial thromboplastin time (aPTT) of a factor VIII inhibitor plasma by 50% of the buffer value (blank value). Excipients with known effect: 500 U FEIBA contains approximately 40 mg sodium per vial. 1000 U FEIBA contains approximately 80 mg sodium per vial. 2500 U FEIBA contains approximately 200 mg sodium per vial. For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Powder and solvent for solution for infusion. White, off-white or pale green powder.The pH value of the ready-to-use solution is between 6.8 and 7.6. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Treatment of bleeding in haemophilia A patients with inhibitors. Treatment of bleeding in haemophilia B patients with inhibitors, if no other specific treatment is available (see section 5.1). Treatment of bleeding in non-haemophiliacs with acquired inhibitors to factor VIII. Läs hela dokumentet