Furosemide Kalceks 10 mg/ ml Norway - Norwegian - Statens legemiddelverk

furosemide kalceks 10 mg/ ml

as kalceks - furosemid - injeksjons-/infusjonsvæske, oppløsning - 10 mg/ ml

Burinex 0.5 mg/ ml Norway - Norwegian - Statens legemiddelverk

burinex 0.5 mg/ ml

karo pharma ab (1) - bumetanid - injeksjonsvæske, oppløsning - 0.5 mg/ ml

Burinex 5 mg Norway - Norwegian - Statens legemiddelverk

burinex 5 mg

karo pharma ab (1) - bumetanid - tablett - 5 mg

Brintellix 10 mg Norway - Norwegian - Statens legemiddelverk

brintellix 10 mg

farmagon - vortioksetinhydrobromid - tablett, filmdrasjert - 10 mg

Aclasta 5 mg Norway - Norwegian - Statens legemiddelverk

aclasta 5 mg

abacus medicine a/s - zoledronsyremonohydrat - infusjonsvæske, oppløsning - 5 mg

Aclasta 5 mg Norway - Norwegian - Statens legemiddelverk

aclasta 5 mg

2care4 aps - zoledronsyremonohydrat - infusjonsvæske, oppløsning - 5 mg

Pepaxti European Union - Norwegian - EMA (European Medicines Agency)

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - multippelt myelom - antineoplastiske midler - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.