Unione Europea - italiano - EMA (European Medicines Agency)

mylan pharmaceuticals limited - fulvestrant - neoplasie al seno - terapia endocrina - fulvestrant è indicato per il trattamento del recettore per gli estrogeni positivi, localmente avanzato o metastatico della mammella in donne in post-menopausa:non precedentemente trattati con terapia endocrina, ocon ricaduta di malattia o dopo coadiuvante anti-estrogeno terapia, o la progressione della malattia sulla terapia antiestrogen.

Unione Europea - italiano - EMA (European Medicines Agency)

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - immunostimolanti, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Unione Europea - italiano - EMA (European Medicines Agency)

astrazeneca ab - sodio zirconio cyclosilicate - iperkaliemia - tutti gli altri prodotti terapeutici - lokelma è indicato per il trattamento di iperkaliemia in pazienti adulti.

Unione Europea - italiano - EMA (European Medicines Agency)

theramex ireland limited - abaloparatide - osteoporosis, postmenopausal; osteoporosis - omeostasi del calcio - trattamento dell'osteoporosi nelle donne in postmenopausa ad aumentato rischio di fratture.

Unione Europea - italiano - EMA (European Medicines Agency)

ferring pharmaceuticals a/s - degarelix - neoplasie prostatiche - terapia endocrina - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Unione Europea - italiano - EMA (European Medicines Agency)

tmc pharma (eu) limited - fosdenopterin hydrobromide dihydrate - metal metabolism, inborn errors - altro apparato digerente e metabolismo prodotti, - nulibry is indicated for the treatment of patients with molybdenum cofactor deficiency (mocd) type a.

Unione Europea - italiano - EMA (European Medicines Agency)

accord healthcare s.l.u. - degarelix acetate - neoplasie prostatiche - other hormone antagonists and related agents - degarelix accord is a gonadotrophin releasing hormone (gnrh) antagonist indicated:for treatment of adult male patients with advanced hormone-dependent prostate cancer. for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.

Unione Europea - italiano - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - maribavir - infezioni da cytomegalovirus - antivirali per uso sistemico - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). dovrebbero essere prese in considerazione le linee guida ufficiali sull'uso appropriato degli agenti antivirali.

Italia - italiano - Ministero della Salute

geister medizintechnik gmbh - divaricatori addominali

Italia - italiano - Ministero della Salute

geister medizintechnik gmbh - divaricatori addominali