Pays: Pays-Bas
Langue: néerlandais
Source: CBG-MEB (College ter Beoordeling van Geneesmiddelen)
FULVESTRANT 50 mg/ml
Zentiva k.s. U kabelovny 130 102 37 PRAGUE 10 (TSJECHIË)
FULVESTRANT 50 mg/ml
Oplossing voor injectie
BENZYLALCOHOL (E 1519) 100 mg/ml ; BENZYLBENZOAAT ; CASTOROLIE ; ETHANOL 96 % 100 mg/ml
Intramusculair gebruik
1900-01-01
26 SPC-FLVS-CC- v05-day 205 PACKAGE LEAFLET 27 SPC-FLVS-CC- v05-day 205 PACKAGE LEAFLET: INFORMATION FOR THE PATIENT Vastaloma 250 mg oplossing voor injectie in een voorgevulde spuit fulvestrant 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, ask your doctor, pharmacist or nurse. - 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, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4. WHAT IS IN THIS LEAFLET 1. What Vastaloma is and what it is used for 2. What you need to know before you are given Vastaloma 3. How Vastaloma will be given 4. Possible side effects 5. How to store Vastaloma 6. Contents of the pack and other information 1. WHAT VASTALOMA IS AND WHAT IT IS USED FOR Vastaloma contains the active substance fulvestrant, which belongs to the group of estrogen blockers. Estrogens, a type of female sex hormones, can in some cases be involved in the growth of breast cancer. Vastaloma is used either: - Alone, to treat postmenopausal women with a type of breast cancer called estrogen receptor positive breast cancer that is locally advanced or has spread to other parts of the body (metastatic), or - In combination with palbociclib to treat women with a type of breast cancer called hormone receptor-positive, human epidermal growth factor receptor 2-negative breast cancer, that is locally advanced or has spread to other parts of the body (metastatic). Women who have not reached menopause will also be treated with a medicine called a luteinizing hormone releasing hormone (LHRH) agonist. When Vastaloma is given in combination with palbociclib, it is important that you also read the package leaflet for palbociclib. If you have any questions about palbociclib, Lire le document complet
1 SPC-FLVS-CC- v05-day 205 SAMENVATTING VAN DE PRODUCTKENMERKEN 2 SPC-FLVS-CC- v05-day 205 1. NAAM VAN HET GENEESMIDDEL Vastaloma 250 mg oplossing voor injectie in een voorgevulde spuit 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each pre-filled syringe of 5 ml contains 250 mg fulvestrant. Excipients with known effect (per 5 ml) Ethanol 96% (alcohol), 500 mg Benzyl alcohol (E1519), 500 mg Benzyl benzoate, 750 mg For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Solution for injection in pre-filled syringe Clear, colorless to yellow, viscous solution, free from visible particles. 4. CLINICAL PARTICULARS 4.1 THERAPEUTIC INDICATIONS Fulvestrant is indicated: - as monotherapy for the treatment of estrogen receptor positive, locally advanced or metastatic breast cancer in postmenopausal women: o not previously treated with endocrine therapy, or o with disease relapse on or after adjuvant antiestrogen therapy, or disease progression on antiestrogen therapy. - in combination with palbociclib for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer in women who have received prior endocrine therapy (see section 5.1). In pre- or perimenopausal women, the combination treatment with palbociclib should be combined with a luteinizing hormone releasing hormone (LHRH) agonist. 4.2 POSOLOGY AND METHOD OF ADMINISTRATION Posology _Adult females (including elderly) _ The recommended dose is 500 mg at intervals of one month, with an additional 500 mg dose given two weeks after the initial dose. When fulvestrant is used in combination with palbociclib, please also refer to the Summary of Product Characteristics of palbociclib. Prior to the start of treatment with the combination of fulvestrant plus palbociclib, and throughout its duration, pre/perimenopausal women should be treated with LHRH agonists according to local clinical practice. 3 SPC-FLVS-CC- v05-day 205 Special population _Renal impairment _ No dose adju Lire le document complet