โš  LIVE โ€” European Consumer Safety Watch ๐Ÿ’Š Etichetta canale medico: 18 negli ultimi 7 giorni ๐ŸŽ Canale alimentare: 180 negli ultimi 7 giorni ๐Ÿงธ Canale: prodotti: 48 negli ultimi 7 giorni ๐ŸŸข Monitoraggio: EMA ยท RASFF ยท NVWA ยท FAGG ยท FAVV ยท EFSA ยท Safety Gate โฑ Ultimo recupero: 1 ora fa โš  LIVE โ€” European Consumer Safety Watch ๐Ÿ’Š Etichetta canale medico: 18 negli ultimi 7 giorni ๐ŸŽ Canale alimentare: 180 negli ultimi 7 giorni ๐Ÿงธ Canale: prodotti: 48 negli ultimi 7 giorni ๐ŸŸข Monitoraggio: EMA ยท RASFF ยท NVWA ยท FAGG ยท FAVV ยท EFSA ยท Safety Gate โฑ Ultimo recupero: 1 ora fa
๐Ÿ›ก๏ธ EUSW
๐Ÿ‡ฎ๐Ÿ‡น
๐Ÿ’Š

Glivec

imatinib
Leucemia linfoblastica acuta a cellule precursori;Tumori stromali gastrointestinali;Dermatofibrosarcoma;Malattie mielodisplastiche-mieloproliferative;Leucemia mieloide cronica BCR-ABL positiva;Sindrome ipereosinofilica
โœ… Autorizzato
โœ…
Nessun allarme attivo
Questo medicinale non presenta carenze in corso, lettere di sicurezza o richiami.

A cosa serve

Glivec is indicated for the treatment of adult and paediatric patients with newly diagnosed Philadelphia-chromosome (bcr-abl)-positive (Ph+) chronic myeloid leukaemia (CML) for whom bone-marrow transplantation is not considered as the first line of treatment; adult and paediatric patients with Ph+ CML in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis; adult and paediatric patients with newly diagnosed Philadelphia-chromosome-positive acute lymphoblastic leukaemia (Ph+ ALL) integrated with chemotherapy; adult patients with relapsed or refractory Ph+ ALL as monotherapy; adult patients with myelodysplastic / myeloproliferative diseases (MDS / MPD) associated with platelet-derived growth factor receptor (PDGFR) gene re-arrangements; adult patients with advanced hypereosinophilic syndrome (HES) and / or chronic eosinophilic leukaemia (CEL) with FIP1L1-PDGFRa rearrangement. The effect of Glivec on the outcome of bone-marrow transplantation has not been determined. Glivec is indicated for: the treatment of adult patients with Kit (CD 117)-positive unresectable and / or metastatic malignant gastrointestinal stromal tumours (GIST); the adjuvant treatment of adult patients who are at significant risk of relapse following resection of Kit (CD117)-positive GIST. Patients who have a low or very low risk of recurrence should not receive adjuvant treatment; the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (DFSP) and adult patients with recurrent and / or metastatic DFSP who are not eligible for surgery. In adult and paediatric patients, the effectiveness of Glivec is based on overall haematological and cytogenetic response rates and progression-free survival in CML, on haematological and cytogenetic response rates in Ph+ ALL, MDS / MPD, on haematological response rates in HES / CEL and on objective response rates in adult patients with unresectable and / or metastatic GIST and DFSP and on recurrence-free survival in adjuvant GIST. The experience with Glivec in patients with MDS / MPD associated with PDGFR gene re-arrangements is very limited (see section 5.1). Except in newly diagnosed chronic phase CML, there are no controlled trials demonstrating a clinical benefit or increased survival for these diseases.

โš ๏ธ Sicurezza del paziente

No

โš ๏ธ Aggregiamo avvisi ufficiali. Non forniamo consulenze mediche. Per decisioni mediche o legali, consulta l'ente di riferimento e un professionista qualificato.