Skyrizi Unia Europejska - polski - EMA (European Medicines Agency)

skyrizi

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - leki immunosupresyjne - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), 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). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.

Byooviz Unia Europejska - polski - EMA (European Medicines Agency)

byooviz

samsung bioepis nl b.v. - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - okulistyka - byooviz 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).

Ranivisio Unia Europejska - polski - EMA (European Medicines Agency)

ranivisio

midas pharma gmbh - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - okulistyka - ranivisio 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).

Ximluci Unia Europejska - polski - EMA (European Medicines Agency)

ximluci

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).

Lucentis Unia Europejska - polski - EMA (European Medicines Agency)

lucentis

novartis europharm limited - ranibizumab - wet macular degeneration; macular edema; diabetes complications; myopia, degenerative; choroidal neovascularization - okulistyka - lucentis jest wskazany u dorosłych w leczeniu wysiękowej postaci (na mokro) związane z wiekiem zwyrodnienie plamki żółtej (amd)leczenie wzroku w wyniku хориоидальной neowaskularyzacji (ХНВ)leczeniu zaburzeń widzenia spowodowanych cukrzycowego obrzęku plamki (ДМО)leczenia zaburzeń widzenia na skutek obrzęku plamki wtórnego zgryzu siatkówkowych żył (oddział lub centralny РВО РВО).

Adakveo Unia Europejska - polski - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anemia, sickle cell - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Eylea Unia Europejska - polski - EMA (European Medicines Agency)

eylea

bayer ag - aflibercept - wet macular degeneration; macular edema; diabetes complications - okulistyka - Эйлеа jest wskazany dla osób dorosłych w celu leczenia:wysiękowej postaci (na mokro) związane z wiekiem zwyrodnienie plamki żółtej (amd);zaburzenia widzenia z powodu obrzęku plamki wtórnego zgryzu siatkówkowych żył (oddział lub centralny РВО РВО);zaburzenia ze względu na cukrzycowego obrzęku plamki (ДМО);zaburzenia ze względu na миопической хориоидальной neowaskularyzacji (миопической ХНВ).

Yesafili Unia Europejska - polski - EMA (European Medicines Agency)

yesafili

viatris limited - aflibercept - macular edema; retinal vein occlusion; diabetic retinopathy; myopia, degenerative; diabetes complications - okulistyka - yesafili is indicated for adults for the treatment ofneovascular (wet) age-related macular degeneration (amd) (see section 5. 1),visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo) (see section 5. 1),visual impairment due to diabetic macular oedema (dme) (see section 5. 1),visual impairment due to myopic choroidal neovascularisation (myopic cnv) (see section 5.

Spevigo Unia Europejska - polski - EMA (European Medicines Agency)

spevigo

boehringer ingelheim international gmbh - spesolimab - Łuszczyca - leki immunosupresyjne - spevigo is indicated for the treatment of flares in adult patients with generalised pustular psoriasis (gpp) as monotherapy.

Ipique Unia Europejska - polski - EMA (European Medicines Agency)

ipique

rotterdam biologics b.v. - bevacizumab - zwyrodnienie plamki żółtej - okulistyka - treatment of neovascular (wet) age-related macular degeneration (amd).