Lacosamide Accord Európai Unió - olasz - EMA (European Medicines Agency)

lacosamide accord

accord healthcare s.l.u. - lacosamide - epilessia - antiepilettici, - lacosamide accord is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. lacosamide accord is indicated as adjunctive therapy•         in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. •         in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Lenalidomide Accord Európai Unió - olasz - EMA (European Medicines Agency)

lenalidomide accord

accord healthcare s.l.u. - lenalidomide - mieloma multiplo - immunosoppressori - multiple myelomalenalidomide accord as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide accord as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) è indicato per il trattamento di pazienti adulti con mieloma multiplo precedentemente non trattato e che non sono idonei per il trapianto. lenalidomide accordo, in combinazione con desametasone, è indicato per il trattamento del mieloma multiplo in pazienti adulti che hanno ricevuto almeno una precedente terapia. follicular lymphomalenalidomide accord in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Posaconazole Accord Európai Unió - olasz - EMA (European Medicines Agency)

posaconazole accord

accord healthcare s.l.u. - posaconazolo - micosi - antimicotici per uso sistemico - posaconazole accord is indicated for use in the treatment of the following fungal infections in adults:invasive aspergillosis;fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. la refrattarietà è definito come la progressione di infezione o di mancata migliorare dopo un minimo di 7 giorni prima di dosi terapeutiche di una efficace terapia antimicotica. posaconazole accordo è anche indicato per la profilassi di infezioni fungine invasive nei seguenti pazienti: i pazienti che ricevono remissione-chemioterapia di induzione per la leucemia mieloide acuta (aml) o sindromi mielodisplastiche (mds) dovrebbe causare neutropenia prolungata e che sono ad alto rischio di sviluppare infezioni fungine invasive;trapianto di cellule staminali ematopoietiche (hsct) destinatari che sono sottoposti ad alte dosi di terapia immunosoppressiva per graft versus host disease e che sono ad alto rischio di sviluppare infezioni fungine invasive.

Deferasirox Accord Európai Unió - olasz - EMA (European Medicines Agency)

deferasirox accord

accord healthcare s.l.u. - deferasirox - iron overload; beta-thalassemia - tutti gli altri prodotti terapeutici, ferro da stiro agenti chelanti - deferasirox accord è indicato per il trattamento del sovraccarico cronico di ferro dovuto a frequenti trasfusioni di sangue (≥7 ml/kg/mese di globuli rossi concentrati) in pazienti con beta talassemia major di età 6 anni e più vecchi. deferasirox accord è indicato anche per il trattamento del sovraccarico cronico di ferro dovuto a emotrasfusioni quando deferoxamina terapia è controindicata o inadeguata nei seguenti gruppi di pazienti:in pazienti pediatrici con beta talassemia major con sovraccarico di ferro dovuto a frequenti trasfusioni di sangue (≥7 ml/kg/mese di globuli rossi concentrati) di età compresa tra 2 a 5 anni in pazienti adulti e pediatrici con beta talassemia major con sovraccarico di ferro dovuto a frequenti emotrasfusioni (.

Azacitidine Accord Európai Unió - olasz - EMA (European Medicines Agency)

azacitidine accord

accord healthcare s.l.u. - azacitidina - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - agenti antineoplastici - azacitidina accord è indicato per il trattamento di pazienti adulti che non sono eleggibili per il trapianto di cellule staminali ematopoietiche (hsct) con:- intermedio-2 e ad alto rischio di sindromi mielodisplastiche (mds) secondo l'international prognostic scoring system (ipss),- leucemia mielomonocitica cronica (cmml) con 10-29 % di midollo esplosioni senza mieloproliferative disturbo,- leucemia mieloide acuta (aml) con 20-30 % di blasti e multi-lineage displasia, secondo l'organizzazione mondiale della sanità (oms) classificazione,- aml con >30% midollo di blasti secondo la classificazione who.

Fampridine Accord Európai Unió - olasz - EMA (European Medicines Agency)

fampridine accord

accord healthcare s.l.u. - fampridine - sclerosi multipla - altri farmaci sul sistema nervoso - fampridine accord is indicated for the improvement of walking in adult patients with multiple sclerosis with walking disability (edss 4-7).

Rivaroxaban Accord Európai Unió - olasz - EMA (European Medicines Agency)

rivaroxaban accord

accord healthcare s.l.u. - rivaroxaban - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - agenti antitrombotici - prevenzione del tromboembolismo venoso (tev) in pazienti adulti sottoposti a chirurgia sostitutiva elettiva dell'anca o del ginocchio. trattamento della trombosi venosa profonda (tvp) ed embolia polmonare (ep) e prevenzione della recidiva di tvp e ep nell'adulto. (see section 4. 4 for haemodynamically unstable pe patients. trattamento della trombosi venosa profonda (tvp) ed embolia polmonare (ep) e prevenzione della recidiva di tvp e ep nell'adulto. (see section 4. 4 per haemodynamically instabile pe pazienti). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. trattamento della trombosi venosa profonda (tvp) ed embolia polmonare (ep) e prevenzione della recidiva di tvp e ep nell'adulto. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 e 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. trattamento della trombosi venosa profonda (tvp) ed embolia polmonare (ep) e prevenzione della recidiva di tvp e ep nell'adulto. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Abiraterone Accord Európai Unió - olasz - EMA (European Medicines Agency)

abiraterone accord

accord healthcare s.l.u. - abiraterone acetato - neoplasie prostatiche - terapia endocrina - abiraterone accord is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicatedthe treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Icatibant Accord Európai Unió - olasz - EMA (European Medicines Agency)

icatibant accord

accord healthcare s.l.u. - icatibant acetate - angioedema, ereditario - other hematological agents - icatibant accord is indicated for symptomatic treatment of acute attacks of hereditary angioedema (hae) in adults, adolescents and children aged 2 years and older, with c1 esterase inhibitor deficiency.

Dasatinib Accord Európai Unió - olasz - EMA (European Medicines Agency)

dasatinib accord

accord healthcare s.l.u. - dasatinib - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - agenti antineoplastici - dasatinib accord is indicated for the treatment of adult patients with:• ph+ acute lymphoblastic leukaemia (all) with resistance or intolerance to prior therapy. dasatinib accord is indicated for the treatment of paediatric patients with:• newly diagnosed ph+ all in combination with chemotherapy.