Land: Irland
Sprache: Englisch
Quelle: HPRA (Health Products Regulatory Authority)
Mycophenolic acid
Novartis Ireland Limited
L04AA; L04AA06
Mycophenolic acid
180 milligram(s)
Gastro-resistant tablet
Product subject to prescription which may be renewed (B)
Selective immunosuppressants; mycophenolic acid
Marketed
2004-07-02
1 PACKAGE LEAFLET: INFORMATION FOR THE USER MYFORTIC ® 180 MG GASTRO-RESISTANT TABLETS mycophenolic acid (as mycophenolate sodium) READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING 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, 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 signs of illness 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. See section 4. WHAT IS IN THIS LEAFLET 1. What Myfortic is and what it is used for 2. What you need to know before you take Myfortic 3. How to take Myfortic 4. Possible side effects 5. How to store Myfortic 6. Contents of the pack and other information 1. WHAT MYFORTIC IS AND WHAT IT IS USED FOR Myfortic contains a substance called mycophenolic acid. This belongs to a group of medicines called immunosuppressants. Myfortic is used to stop the body’s immune system from rejecting a kidney transplant. It is used together with other medicines containing ciclosporin and corticosteroids. 2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE MYFORTIC WARNING Mycophenolate causes birth defects and miscarriage. If you are a woman who could become pregnant, you must provide a negative pregnancy test before starting treatment and must follow the contraception advice given to you by your doctor. Your doctor will speak to you and give you written information, particularly on the effects of mycophenolate on unborn babies. Read the information carefully and follow the instructions. If you do not fully understand these instructions, please ask your doctor to explain them again before you take mycophenolate. See also further information in this section under “Warnings and precautions” and “Pregnancy and breast-feeding”. DO NOT TAKE MYFORTIC: - if you are allergic to mycophenoli Lesen Sie das vollständige Dokument
Health Products Regulatory Authority 30 January 2023 CRN00CTF3 Page 1 of 13 SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT Myfortic 180 mg gastro-resistant tablets 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each gastro-resistant tablet contains 180 mg mycophenolic acid (as mycophenolate sodium). Excipients with known effect: Lactose : 45 mg per tablet. For the full list of excipients, see section 6.1. 3 PHARMACEUTICAL FORM Gastro-resistant tablet Lime green, film-coated round tablet, with bevelled edges and the imprint (debossing) “C” on one side. 4 CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Myfortic is indicated in combination with ciclosporin and corticosteroids for the prophylaxis of acute transplant rejection in adult patients receiving allogeneic renal transplants. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Treatment with Myfortic should be initiated and maintained by appropriately qualified transplant specialists. Posology The recommended dose is 720 mg administered twice daily (1,440 mg daily dose). This dose of mycophenolate sodium corresponds to 1 g mycophenolate mofetil administered twice daily (2 g daily dose) in terms of mycophenolic acid (MPA) content. For additional information about the corresponding therapeutic doses of mycophenolate sodium and mycophenolate mofetil, see sections 4.4 and 5.2. In _de novo_ patients, Myfortic should be initiated within 72 hours following transplantation. _Special population_ _Paediatric population_ Insufficient data are available to support the efficacy and safety of Myfortic in children and adolescents. Limited pharmacokinetic data are available for paediatric renal transplant patients (see section 5.2). _Older people_ The recommended dose in elderly patients is 720 mg twice daily. _Patients with renal impairment_ In patients experiencing delayed renal graft function post-operatively, no dose adjustments are needed (see section 5.2). Patients with severe renal impairment (glomerular filtration rate <25 ml·min -1 ·1.73 m -2 ) should be Lesen Sie das vollständige Dokument