Oxbryta Evropská unie - čeština - 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.

Tepmetko Evropská unie - čeština - EMA (European Medicines Agency)

tepmetko

merck europe b.v. - tepotinib hydrochloride monohydrate - karcinom, plicní jiná než malobuněčná - antineoplastická činidla - tepmetko as monotherapy is indicated for the treatment of adult patients with advanced non-small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal-epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum-based chemotherapy.

Lupkynis Evropská unie - čeština - EMA (European Medicines Agency)

lupkynis

otsuka pharmaceutical netherlands b.v. - voclosporin - lupus nephritis - imunosupresiva - lupkynis is indicated in combination with mycophenolate mofetil for the treatment of adult patients with active class iii, iv or v (including mixed class iii/v and iv/v) lupus nephritis (ln).

Sunlenca Evropská unie - čeština - EMA (European Medicines Agency)

sunlenca

gilead sciences ireland unlimited company - lenacapavir sodium - hiv infekce - antivirotika pro systémové použití - sunlenca injection, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen (see sections 4. 2 a 5. sunlenca tablet, in combination with other antiretroviral(s), is indicated for the treatment of adults with multidrug resistant hiv 1 infection for whom it is otherwise not possible to construct a suppressive anti viral regimen, for oral loading prior to administration of long-acting lenacapavir injection (see sections 4. 2 a 5.

Mycapssa Evropská unie - čeština - EMA (European Medicines Agency)

mycapssa

amryt pharmaceuticals dac - octreotide acetate - acromegalie - hypofýzy a hypotalamické hormony a analogy - mycapssa is indicated for maintenance treatment in adult patients with acromegaly who have responded to and tolerated treatment with somatostatin analogues.

Vafseo Evropská unie - čeština - EMA (European Medicines Agency)

vafseo

akebia europe limited - vadadustat - renal insufficiency, chronic; anemia - antianemické přípravky - vafseo is indicated for the treatment of symptomatic anaemia associated with chronic kidney disease (ckd) in adults on chronic maintenance dialysis.

CONTROLOC 20MG Enterosolventní tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

controloc 20mg enterosolventní tableta

takeda gmbh, konstanz array - 14061 seskvihydrÁt sodnÉ soli pantoprazolu - enterosolventní tableta - 20mg - pantoprazol

CONTROLOC 40MG Prášek pro injekční roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

controloc 40mg prášek pro injekční roztok

takeda gmbh, konstanz array - 15923 sodnÁ sŮl pantoprazolu - prášek pro injekční roztok - 40mg - pantoprazol

CONTROLOC 40MG Enterosolventní tableta Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

controloc 40mg enterosolventní tableta

takeda gmbh, konstanz array - 14061 seskvihydrÁt sodnÉ soli pantoprazolu - enterosolventní tableta - 40mg - pantoprazol