Tsjechië - Tsjechisch - SUKL (Státní ústav pro kontrolu léčiv)

curium netherlands b.v., petten array - 9673 chlorid thallnÝ-(201tl) - injekční roztok - 37mbq/ml - chlorid thallnÝ-(201tl)

Tsjechië - Tsjechisch - SUKL (Státní ústav pro kontrolu léčiv)

curium netherlands b.v., petten array - 3122 dihydrÁt chloridu cÍnatÉho - kit pro radiofarmakum - 96mcg - technecium-(99mtc) sn2+ Činidla, pro znaČenÍ bunĚk

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

taiho pharma netherlands b.v. - futibatinib - cholangiocarcinoma - cytostatika - lytgobi monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - infekce dýchacích syncyciálních virů - vakcíny - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. použití této vakcíny musí být v souladu s oficiálními doporučeními.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - cedazuridine, decitabine - leukemie, myeloid - antineoplastická činidla - inaqovi is indicated as monotherapy for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) who are ineligible for standard induction chemotherapy.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

aop orphan pharmaceuticals gmbh - ropeginterferon alfa-2b - polycythemia vera - imunostimulancia, - besremi je indikován jako monoterapie u dospělých pro léčbu po polycytemii vera bez symptomatická splenomegalie.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

ucb pharma ltd - natriumoxybutyrát - cataplexy; narcolepsy - další léky na nervový systém - léčba narkolepsie s kataplexií u dospělých pacientů.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

d&a pharma - natriumoxybutyrát - substance withdrawal syndrome; alcohol abstinence - další léky na nervový systém - substitution treatment for alcohol dependence within a framework of careful medical supervision along with continuous psychosocial support and social rehabilitation. treatment should be initiated only in patients resistant to existing interventions or in patients for whom existing therapies are contra-indicated or not recommended.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

novartis europharm limited - crizanlizumab - anémie, kosáčková buňka - 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.

Europese Unie - Tsjechisch - EMA (European Medicines Agency)

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.