Siklos Europska Unija - hrvatski - EMA (European Medicines Agency)

siklos

theravia - hidroksikarbamid - anemija, sickle cell - antineoplastična sredstva - Шиклоше je indiciran za prevenciju рецидивирующих boli сосудисто-jamice кризов, uključujući akutni sindrom grudnog koša kod djece i odraslih pacijenata koji boluju od simptomatske anemija srpastih stanica sindrom.

Xromi Europska Unija - hrvatski - EMA (European Medicines Agency)

xromi

nova laboratories ireland limited - hidroksikarbamid - anemija, sickle cell - antineoplastična sredstva - prevencija сосудисто-jamice komplikacija anemija srpastih stanica anemije u bolesnika starijih od 2 godine.

Xybaid 500 mg tvrde kapsule Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

xybaid 500 mg tvrde kapsule

makpharm d.o.o., trnjanska cesta 37/1, zagreb, hrvatska - hidroksikarbamid - kapsula, tvrda - 500 mg - urbroj: jedna kapsula sadrži 500 mg hidroksikarbamida

Litalir 500 mg tvrde kapsule Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

litalir 500 mg tvrde kapsule

cheplapharm arzneimittel gmbh, ziegelhof 24, greifswald, njemačka - hidroksikarbamid - kapsula, tvrda - 500 mg - urbroj: jedna tvrda kapsula sadrži 500 mg hidroksikarbamida

Oxbryta Europska Unija - hrvatski - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Adakveo Europska Unija - hrvatski - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anemija, sickle cell - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Besremi Europska Unija - hrvatski - EMA (European Medicines Agency)

besremi

aop orphan pharmaceuticals gmbh - ropeginterferon alfa-2b - istinska Полицитемия - Иммуностимуляторы, - besremi prikazan kao monoterapija kod odraslih za liječenje полицитемия vjera bez simptomatske спленомегалии.

Tibsovo Europska Unija - hrvatski - EMA (European Medicines Agency)

tibsovo

les laboratoires servier - ivosidenib - leukemia, myeloid, acute; cholangiocarcinoma - antineoplastična sredstva - tibsovo in combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) with an isocitrate dehydrogenase-1 (idh1) r132 mutation who are not eligible to receive standard induction chemotherapy (see section 5. tibsovo monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with an idh1 r132 mutation who were previously treated by at least one prior line of systemic therapy.

Jakavi Europska Unija - hrvatski - EMA (European Medicines Agency)

jakavi

novartis europharm limited - ruxolitinib (kao fosfat) - myeloproliferative disorders; polycythemia vera; graft vs host disease - antineoplastična sredstva - myelofibrosis (mf)jakavi is indicated for the treatment of disease related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. Полицитемия vjera (mf)jakavi indiciran za liječenje odraslih bolesnika s полицитемия vjera, koje su otporne na ili netoleranciju hidroksiurea. graft versus host disease (gvhd)jakavi is indicated for the treatment of patients aged 12 years and older with acute graft versus host disease or chronic graft versus host disease who have inadequate response to corticosteroids or other systemic therapies (see section 5.