Zoledronic acid Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

zoledronic acid mylan

mylan pharmaceuticals limited - acido zoledronico - fratture, ossa - farmaci per il trattamento delle malattie ossee - prevenzione di eventi correlati all'apparato scheletrico (fratture patologiche, schiacciamenti vertebrali, radioterapia o interventi chirurgici all'osso, ipercalcemia neoplastica) in pazienti adulti affetti da tumori maligni allo stadio avanzato che interessano l'osso;il trattamento di pazienti adulti affetti da ipercalcemia neoplastica (tih).

Zonisamide Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

zonisamide mylan

mylan pharmaceuticals limited - zonisamide - epilessia - antiepilettici, - in monoterapia nel trattamento delle crisi parziali con o senza secondaria generalizzazione in adulti con epilessia di nuova diagnosi;terapia aggiuntiva nel trattamento delle crisi parziali con o senza secondaria generalizzazione in adulti, adolescenti e bambini di età compresa tra i 6 anni e sopra.

Gefitinib Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

gefitinib mylan

mylan pharmaceuticals limited - gefitinib - carcinoma, polmone non a piccole cellule - antineoplastic agents, protein kinase inhibitors - gefitinib mylan è indicato come monoterapia per il trattamento di pazienti adulti con carcinoma localmente avanzato o metastatico non a piccole cellule del polmone (nsclc) con mutazioni attivanti dell'egfr‑tk.

Ambrisentan Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

ambrisentan mylan

mylan s.a.s - ambrisentan - ipertensione, polmonare - antipertensivi, - ambrisentan mylan è indicato per il trattamento dell'ipertensione arteriosa polmonare (pah) in pazienti adulti di che classe funzionale (fc) ii, iii, compreso l'uso in combinazione per il trattamento. l'efficacia è stata dimostrata in ipa idiopatica (ipah) e in ipa associata a malattia del tessuto connettivo. ambrisentan mylan è indicato per il trattamento dell'ipertensione arteriosa polmonare (pah) in pazienti adulti di che classe funzionale (fc) ii, iii, compreso l'uso in combinazione per il trattamento. l'efficacia è stata dimostrata in ipa idiopatica (ipah) e in ipa associata a malattia del tessuto connettivo.

Deferasirox Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

deferasirox mylan

mylan pharmaceuticals limited - deferasirox - iron overload; beta-thalassemia - agenti chelanti del ferro - deferasirox mylan 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 olderthe 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 Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

azacitidine mylan

mylan ireland limited - azacitidina - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - agenti antineoplastici - azacitidine mylan is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with:intermediate 2 and high risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29% marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30% blasts and multi lineage dysplasia, according to world health organisation (who) classification,aml with > 30% marrow blasts according to the who classification.

Abiraterone Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

abiraterone mylan

mylan ireland limited - abiraterone acetato - neoplasie prostatiche - endocrine therapy, other hormone antagonists and related agents - abiraterone mylan 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 indicated. the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel based chemotherapy regimen.

Rivaroxaban Viatris (previously Rivaroxaban Mylan) Uni Eropa - Italia - EMA (European Medicines Agency)

rivaroxaban viatris (previously rivaroxaban mylan)

mylan ireland limited - rivaroxaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - agenti antitrombotici - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan 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.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention 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. paediatric population treatment 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. paediatric population treatment 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.

Dimethyl fumarate Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

dimethyl fumarate mylan

mylan ireland limited - dimetilfumarato - sclerosi multipla recidivante-remittente - immunosoppressori - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Teriflunomide Mylan Uni Eropa - Italia - EMA (European Medicines Agency)

teriflunomide mylan

mylan pharmaceuticals limited - teriflunomide - sclerosi multipla recidivante-remittente - immunosoppressori - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).