Verkazia Unione Europea - italiano - EMA (European Medicines Agency)

verkazia

santen oy - ciclosporina - conjunctivitis; keratitis - oftalmologici - il trattamento di gravi cheratocongiuntivite vernal (vkc) nei bambini a partire dai 4 anni di età e negli adolescenti.

Byooviz Unione Europea - italiano - EMA (European Medicines Agency)

byooviz

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

Ximluci Unione Europea - italiano - EMA (European Medicines Agency)

ximluci

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - oftalmologici - 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).

Ranivisio Unione Europea - italiano - EMA (European Medicines Agency)

ranivisio

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

Gliolan Unione Europea - italiano - EMA (European Medicines Agency)

gliolan

photonamic gmbh & co. kg - 5-aminolevulinico acido cloridrato - glioma - agenti antineoplastici - gliolan è indicato nei pazienti adulti per la visualizzazione di tessuto maligno durante l'intervento chirurgico per glioma maligno (grado iii e iv dell'organizzazione mondiale della sanità).

Enhertu Unione Europea - italiano - EMA (European Medicines Agency)

enhertu

daiichi sankyo europe gmbh - trastuzumab deruxtecan - neoplasie al seno - agenti antineoplastici - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Ikervis Unione Europea - italiano - EMA (European Medicines Agency)

ikervis

santen oy - ciclosporina - malattie della cornea - oftalmologici - trattamento della cheratite grave in pazienti adulti con malattia dell'occhio secco, che non è migliorata nonostante il trattamento con sostituti lacrimali.

Ikervis 1 mg/ml collirio emulsione (dose singola) Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

ikervis 1 mg/ml collirio emulsione (dose singola)

santen sa - ciclosporinum - 1 mg/ml collirio emulsione (dose singola) - ciclosporinum 1 mg, triglycerida media, tyloxapolum, glycerolum, poloxamerum 188, cetalkonii chloridum, natrii hydroxidum, aqua ad iniectabile, ad emulsionem pro 1 ml. - cheratite - synthetika

MERBROMINA SELLA Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

merbromina sella

laboratorio chimico farmaceutico a. sella s.r.l. - merbromina - merbromina