UPLIZNA süste-/infusioonilahuse kontsentraat Estija - estų - Ravimiamet

uplizna süste-/infusioonilahuse kontsentraat

horizon therapeutics ireland designated activity company - inebilizumab - süste-/infusioonilahuse kontsentraat - 10mg 1ml 10ml 3tk

Cleave® Estija - estų - Adama

cleave®

adama - suspo-emulsioon - florasulaam + fluroksüpüür - herbitsiidid

Mixin® Estija - estų - Adama

mixin®

adama - suspo-emulsioon - florasulaam + fluroksüpüür - herbitsiidid

Zoledronic acid Teva Generics Europos Sąjunga - estų - EMA (European Medicines Agency)

zoledronic acid teva generics

teva generics b.v - zoledroonhappe monohüdraat - osteoporosis; osteitis deformans - bisfosfonaadid - ravi osteoporosisin post-menopausis womenin täiskasvanud menat suurenenud risk luumurdude, sealhulgas hiljutine väike-trauma hip-murd. ravi osteoporoosi seotud pikaajalise süsteemse glükokortikoidi therapyin post-menopausis womenin täiskasvanud menat suurenenud risk luumurdude. ravi paget tõbi, luu täiskasvanutel.

Zoledronic acid Teva Pharma Europos Sąjunga - estų - EMA (European Medicines Agency)

zoledronic acid teva pharma

teva b.v. - zoledroonhape - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - narkootikumid luuhaiguste raviks - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture including those with a recent low-trauma hip fracture. treatment of osteoporosis associated with long-term systemic glucocorticoid therapy: , in post-menopausal women;, in men; , at increased risk of fracture. ravi paget tõbi, luu täiskasvanutel.

Pepaxti Europos Sąjunga - estų - EMA (European Medicines Agency)

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - mitu müeloomit - antineoplastilised ained - 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.