Gadovist 1 mmol/ ml Norge - norsk - Statens legemiddelverk

gadovist 1 mmol/ ml

bayer ab - solna - gadobutrol - injeksjonsvæske, oppløsning - 1 mmol/ ml

Gadovist 1 mmol/ ml Norge - norsk - Statens legemiddelverk

gadovist 1 mmol/ ml

bayer ab - solna - gadobutrol - injeksjonsvæske, oppløsning - 1 mmol/ ml

Moxonidin Actavis 0.2 mg Norge - norsk - Statens legemiddelverk

moxonidin actavis 0.2 mg

actavis group ptc ehf (1) - moksonidin - tablett, filmdrasjert - 0.2 mg

Moxonidin Actavis 0.4 mg Norge - norsk - Statens legemiddelverk

moxonidin actavis 0.4 mg

actavis group ptc ehf (1) - moksonidin - tablett, filmdrasjert - 0.4 mg

Primovist 0.25 mmol/ ml Norge - norsk - Statens legemiddelverk

primovist 0.25 mmol/ ml

bayer ab - solna - dinatriumgadoksetat - injeksjonsvæske, oppløsning i ferdigfylt sprøyte - 0.25 mmol/ ml

Yescarta Den europeiske union - norsk - EMA (European Medicines Agency)

yescarta

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastiske midler - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Zynteglo Den europeiske union - norsk - EMA (European Medicines Agency)

zynteglo

bluebird bio (netherlands) b.v. - autologous cd34+ celle beriket befolkningen som inneholder blodkreft stamceller transduced med lentiglobin bb305 lentiviral vektor koding av beta-en-t87q-globin-genet - beta-thalassemia - other hematological agents - zynteglo er indisert for behandling av pasienter som er 12 år og eldre med transfusjon-avhengige β thalassaemia (tdt) som ikke har en β0/β0 genotype, for hvem haematopoietic stilk cellen (hsc) transplantasjon er riktig, men en human leukocyte antigen (hla)-matchet i slekt hsc donor er ikke tilgjengelig.

Reblozyl Den europeiske union - norsk - EMA (European Medicines Agency)

reblozyl

bristol myers squibb pharma eeig - luspatercept - anemia; myelodysplastic syndromes; beta-thalassemia - andre antianemic preparations - reblozyl is indicated for the treatment of adult patients with transfusion-dependent anaemia due to very low, low and intermediate-risk myelodysplastic syndromes (mds) with ring sideroblasts, who had an unsatisfactory response to or are ineligible for erythropoietin-based therapy (see section 5. reblozyl is indicated in adults for the treatment of anaemia associated with transfusion dependent and non transfusion dependent beta thalassaemia (see section 5.

Tecartus Den europeiske union - norsk - EMA (European Medicines Agency)

tecartus

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - lymfom, mantelcelle - antineoplastiske midler - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Libmeldy Den europeiske union - norsk - EMA (European Medicines Agency)

libmeldy

orchard therapeutics (netherlands) bv - atidarsagene autotemcel - leukodystrophy, metachromatic - andre nervesystemet narkotika - libmeldy is indicated for the treatment of metachromatic leukodystrophy (mld) characterized by biallelic mutations in the arysulfatase a (arsa) gene leading to a reduction of the arsa enzymatic activity:in children with late infantile or early juvenile forms, without clinical manifestations of the disease,in children with the early juvenile form, with early clinical manifestations of the disease, who still  have the ability to walk independently and before the onset of cognitive decline.