Morphasol vet 10 mg/ ml Norge - norsk - Statens legemiddelverk

morphasol vet 10 mg/ ml

animedica gmbh - butorfanol - injeksjonsvæske, oppløsning - 10 mg/ ml

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

kapruvia

vifor fresenius medical care renal pharma france - difelikefalin - pruritus - alle andre terapeutiske produkter - kapruvia is indicated for the treatment of moderate-to-severe pruritus associated with chronic kidney disease in adult patients on haemodialysis (see section 5.

Butomidor vet 10 mg/ ml Norge - norsk - Statens legemiddelverk

butomidor vet 10 mg/ ml

vetviva richter gmbh - butorfanoltartrat - injeksjonsvæske, oppløsning - 10 mg/ ml

Morphasol vet 4 mg/ ml Norge - norsk - Statens legemiddelverk

morphasol vet 4 mg/ ml

animedica gmbh - butorfanol - injeksjonsvæske, oppløsning - 4 mg/ ml

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

poteligeo

kyowa kirin holdings b.v. - mogamulizumab - sezary syndrome; mycosis fungoides - antineoplastiske midler - poteligeo er indisert for behandling av voksne pasienter med mycosis fungoides (mf) eller sézary syndrom (ss) som har mottatt minst én tidligere systemisk terapi.

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

veklury

gilead sciences ireland uc - remdesivir - covid-19 virus infection - veklury is indicated for the treatment of coronavirus disease 2019 (covid 19) in:adults and paediatric patients (at least 4 weeks of age and weighing at least 3 kg) with pneumonia requiring supplemental oxygen (low- or high-flow oxygen or other non-invasive ventilation at start of treatment)adults and paediatric patients (weighing at least 40 kg) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

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

sarclisa

sanofi winthrop industrie - isatuximab - multippelt myelom - antineoplastiske midler - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

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

regkirona

celltrion healthcare hungary kft. - regdanvimab - covid-19 virus infection - immune sera og immunglobuliner, - regdanvimab is indicated for the treatment of adults with coronavirus disease 2019 (covid-19) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

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

evusheld

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.