Európska únia - poľština - EMA (European Medicines Agency)

astrazeneca ab - moxetumomab pasudotox - białaczka, włochate komórki - Środki przeciwnowotworowe - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Európska únia - poľština - EMA (European Medicines Agency)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - szczepionki - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. stosowanie tej szczepionki powinno odbywać się zgodnie z oficjalnymi zaleceniami.

Európska únia - poľština - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - dostarlimab - endometrial neoplasms - antineoplastic agents and antibody drug conjugates - jemparli is indicated as monotherapy for the treatment of adult patients with mismatch repair deficient (dmmr)/microsatellite instability-high (msi h) recurrent or advanced endometrial cancer (ec) that has progressed on or following prior treatment with a platinum-containing regimen.

Európska únia - poľština - EMA (European Medicines Agency)

roche registration gmbh - satralizumab - neuromyelitis optica - leki immunosupresyjne - satralizumab (enspryng) is indicated as a monotherapy or in combination with immunosuppressive therapy (ist) for the treatment of neuromyelitis optica spectrum disorders (nmosd) in adult and adolescent patients from 12 years of age who are anti-aquaporin-4 igg (aqp4-igg) seropositive.

Európska únia - poľština - EMA (European Medicines Agency)

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - odporne surowicy i immunoglobuliny, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.

Európska únia - poľština - EMA (European Medicines Agency)

roche registration gmbh - faricimab - wet macular degeneration; macular edema; diabetes complications - okulistyka - vabysmo is indicated for the treatment of adult patients with:neovascular (wet) age-related macular degeneration (namd),visual impairment due to diabetic macular oedema (dme).

Európska únia - poľština - EMA (European Medicines Agency)

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - Środki przeciwnowotworowe - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.

Európska únia - poľština - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - insulin human - Инсулины i analogi do wstrzykiwań, pośredniego działania - cats; dogs - w leczeniu cukrzycy u kotów i psów na celu zmniejszenie hiperglikemii i poprawy powiązanych objawów klinicznych.

Európska únia - poľština - EMA (European Medicines Agency)

astrazeneca ab - anifrolumab - liszaj rumieniowaty, układowy - leki immunosupresyjne - saphnelo is indicated as an add-on therapy for the treatment of adult patients with moderate to severe, active autoantibody-positive systemic lupus erythematosus (sle), despite standard therapy.

Európska únia - poľština - EMA (European Medicines Agency)

argenx - efgartigimod alfa - myasthenia gravis - leki immunosupresyjne - vyvgart is indicated as an add on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gmg) who are anti acetylcholine receptor (achr) antibody positive.