Poland - Poland - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

stada arzneimittel ag - solifenacini succinas - tabletki powlekane - 10 mg

Poland - Poland - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

stada arzneimittel ag - emtricitabinum + tenofovirum disoproxilum - tabletki powlekane - 200 mg + 245 mg

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

ucb pharma s.a. - lakozamid - padaczka, częściowa - przeciwpadaczkowe narzędzia, - producent ukb jest wskazany w monoterapii i terapii wspomagającej w leczeniu napadów częściowych napadów padaczkowych, z lub bez wtórnego uogólnienia u dorosłych, młodzieży i dzieci w wieku od 4 lat z padaczką.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

ucb pharma s.a. - romosozumab - osteoporoza - leki stosowane w leczeniu chorób kości - evenity jest wskazany w leczeniu ciężkich postaci osteoporozy u kobiet po menopauzie z wysokim ryzykiem złamań.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

instituto grifols s.a. - Динатриевая fostamatinib - małopłytkowość - inne systemowe leki ściągające - tavlesse jest wskazany do leczenia przewlekłego małopłytkowości immunologicznej (itp) u dorosłych pacjentów, oporne na inne metody leczenia.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

dynavax gmbh - antygen powierzchniowy wirusa zapalenia wątroby typu b - zapalenie wątroby typu b - szczepionki - heplisav b is indicated for the active immunisation against hepatitis b virus infection (hbv) caused by all known subtypes of hepatitis b virus in adults 18 years of age and older. the use of heplisav b should be in accordance with official recommendations. it can be expected that hepatitis d will also be prevented by immunisation with heplisav b as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

ucb pharma s.a.   - bimekizumab - Łuszczyca - leki immunosupresyjne - plaque psoriasisbimzelx is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisbimzelx, alone or in combination with methotrexate, is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)bimzelx is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri) who have responded inadequately or are intolerant to non-steroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)bimzelx is indicated for the treatment of adults with active ankylosing spondylitis who have responded inadequately or are intolerant to conventional therapy.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

stada arzneimittel ag - budesonide, micronised - glomerulonephritis, iga - przeciw rozwolnieniem, patogenów jelitowych przeciwzapalne / antiinfective - kinpeygo is indicated for the treatment of primary immunoglobulin a (iga) nephropathy (igan) in adults at risk of rapid disease progression with a urine protein-to-creatinine ratio (upcr) ≥1. 5 g/gram.

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - okulistyka - ximluci is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

Kesatuan Eropah - Poland - EMA (European Medicines Agency)

novartis europharm limited  - gozetotide - obrazowanie radionuklidami - diagnostyczne radiofarmaceutyki - ten produkt leczniczy jest przeznaczony wyłącznie do celów diagnostycznych. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.