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

polivy

roche registration gmbh - polatuzumab vedotin - lymfom, b-celle - antineoplastiske midler - polivy i kombinasjon med bendamustine og rituximab er indisert for behandling av voksne pasienter med tilbakefall/ildfast diffuse store b-celle lymfom (dlbcl) som ikke er kandidater for haematopoietic stamcelletransplantasjon. polivy in combination with rituximab, cyclophosphamide, doxorubicin, and prednisone (r-chp) is indicated for the treatment of adult patients with previously untreated diffuse large b-cell lymphoma (dlbcl).

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

lunsumio

roche registration gmbh - mosunetuzumab - lymfom, follikulært - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

Pantecta Control Den europeiske union - norsk - EMA (European Medicines Agency)

pantecta control

takeda gmbh - pantoprazol - gastroøsofageal refluks - proton pumpen inhibitors - kortsiktig behandling av reflukssymptomer (f.eks. halsbrann, syreregurgitasjon) hos voksne.

Gentamicin B. Braun 3 mg/ ml Norge - norsk - Statens legemiddelverk

gentamicin b. braun 3 mg/ ml

b. braun melsungen ag - gentamicinsulfat - infusjonsvæske, oppløsning - 3 mg/ ml

Gentamicin B. Braun 1 mg/ ml Norge - norsk - Statens legemiddelverk

gentamicin b. braun 1 mg/ ml

b. braun melsungen ag - gentamicinsulfat - infusjonsvæske, oppløsning - 1 mg/ ml

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

pombiliti

amicus therapeutics europe limited - cipaglucosidase alfa - glykogen storage sykdom type ii - andre alimentary tract and metabolism products, - pombiliti (cipaglucosidase alfa) is a long-term enzyme replacement therapy used in combination with the enzyme stabiliser miglustat for the treatment of adults with late-onset pompe disease (acid α-glucosidase [gaa] deficiency).

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

pixuvri

les laboratoires servier - pixantron dimaleat - lymfom, ikke-hodgkin - antineoplastiske midler - pixuvri er indisert som monoterapi for behandling av voksne pasienter med multiplikasjon av tilbakefallende eller ildfaste aggressive, ikke-hodgkin b-celle lymfomer (nhl). fordelen med pixantronbehandling er ikke fastslått hos pasienter når de brukes som femte linje eller større kjemoterapi hos pasienter som er ildfaste mot siste behandling.

Talmanco (previously Tadalafil Generics) Den europeiske union - norsk - EMA (European Medicines Agency)

talmanco (previously tadalafil generics)

viatris limited - tadalafil - hypertensjon, pulmonal - urologika - talmanco er indisert hos voksne til behandling av pulmonal arteriell hypertensjon (pah) klassifisert som who-funksjonsklasse ii og iii, for å forbedre treningskapasiteten. effekt har blitt vist i idiopatisk pah (ipah) og i pah relatert til kollagenvaskulær sykdom.

Thiotepa Riemser Den europeiske union - norsk - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - tiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastiske midler - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

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

lonsurf

les laboratoires servier - trifluridine, tipiracil hydrochloride - colorektale neoplasmer - antineoplastiske midler - colorectal cancerlonsurf is indicated in combination with bevacizumab for the treatment of adult patients with metastatic colorectal cancer (crc) who have received two prior anticancer treatment regimens including fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapies, anti-vegf agents, and/or anti-egfr agents. lonsurf is indicated as monotherapy for the treatment of adult patients with metastatic colorectal cancer (crc) who have been previously treated with, or are not considered candidates for, available therapies including fluoropyrimidine-, oxaliplatin- and irinotecan-based chemotherapies, anti-vegf agents, and anti egfr agentsgastric cancerlonsurf is indicated as monotherapy for the treatment of adult patients with metastatic gastric cancer including adenocarcinoma of the gastroesophageal junction, who have been previously treated with at least two prior systemic treatment regimens for advanced disease.