voriconazole sciecure 200 mg pulveris infūziju šķīduma pagatavošanai
sciecure pharma ltd, united kingdom - vorikonazols - pulveris infūziju šķīduma pagatavošanai - 200 mg
fulvestrant accord 250 mg šķīdums injekcijām pilnšļircē
accord healthcare b.v., netherlands - fulvestrants - Šķīdums injekcijām pilnšļircē - 250 mg
giapreza
paion deutschland gmbh - angiotensīna ii acetāts - hypotension; shock - agents, kas iedarbojas uz renīna-angiotenzīna sistēmu - giapreza ir indicēts, lai ārstētu ugunsizturīgo hipotensija pieaugušajiem ar septisko vai citu sadales šoks, kas paliek hypotensive neskatoties uz atbilstoša apjoma atgūšanas un piemērošanu, kateholamīnu, un citus pieejamus vasopressor terapiju.
givlaari
alnylam netherlands b.v. - givosiran - porphyrias, aknu - dažādi gremošanas traktu un vielmaiņu ietekmējošie līdzekļi - Ārstēšana akūtas aknu porphyria (ahp) pieaugušajiem un pusaudžiem vecumā no 12 gadiem un vecāki.
oxlumo
alnylam netherlands b.v. - lumasiran sodium - hyperoxaluria, primary - citas gremošanas trakta un metabolisma produkti, - treatment of primary hyperoxaluria type 1 (ph1) in all age groups.
pku cooler® red 15 šķidrums
vitaflo france 320771967 38 rue de berri 75008 parīze, francija - Šķidrums - īpašiem medicīniskiem nolūkiem paredzēta pārtika - pku cooler® red 15 ir lietošanai gatavs fenilalanīnu nesaturošs,* olbaltumvielas aizvietojošs dzēriens, kas satur neaizvietojamās un aizvietojamās aminoskābes, ogļhidrātus, vitamīnus, minerālvielas, mikroelementus un dokozaheksaēnskābi (dha). uztura režīms pierādītas fenilketonūrijas (pku) gadījumā bērniem no 3 gadu vecuma un pieaugušajiem.
nexpovio
stemline therapeutics b.v. - selinexor - multiple mieloma - antineoplastiski līdzekļi - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.
fulvestrant stada 250 mg šķīdums injekcijām pilnšļircē
stada arzneimittel ag, germany - fulvestrants - Šķīdums injekcijām pilnšļircē - 250 mg/5 ml
tabrecta
novartis europharm limited - capmatinib dihydrochloride monohydrate - karcinoma, nesīkšūnu plaušas - antineoplastiski līdzekļi - tabrecta 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.
cevenfacta
laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemorāģija - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.