Eileen 60 mikrogrami/13 mikrogrami/24 stundās transdermāls plāksteris Latvija - latviešu - Zāļu valsts aģentūra

eileen 60 mikrogrami/13 mikrogrami/24 stundās transdermāls plāksteris

gedeon richter plc., hungary - gestodenum, ethinylestradiolum - transdermāls plāksteris - 60 µg/13 µg/24 stundās

Celdoxome pegylated liposomal Eiropas Savienība - latviešu - EMA (European Medicines Agency)

celdoxome pegylated liposomal

yes pharmaceutical development services gmbh - doksorubicīna hidrohlorīds - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - antineoplastiski līdzekļi - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).

Celsentri Eiropas Savienība - latviešu - EMA (European Medicines Agency)

celsentri

viiv healthcare b.v. - maraviroc - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - celsentri, in combination with other antiretroviral medicinal products, is indicated for treatment experienced adults, adolescents and children of 2 years of age and older and weighing at least 10 kg infected with only ccr5-tropic hiv-1 detectable,.

Vipdomet Eiropas Savienība - latviešu - EMA (European Medicines Agency)

vipdomet

takeda pharma a/s - alogliptin benzoāts, metformīns hidrohlorīds - cukura diabēts, 2. tips - drugs used in diabetes, combinations of oral blood glucose lowering drugs - vipdomet is indicated in the treatment of adult patients aged 18 years and older with type-2 diabetes mellitus:as an adjunct to diet and exercise to improve glycaemic control in adult patients, inadequately controlled on their maximal tolerated dose of metformin alone, or those already being treated with the combination of alogliptin and metformin;in combination with pioglitazone (i. triple combination therapy) as an adjunct to diet and exercise in adult patients inadequately controlled on their maximal tolerated dose of metformin and pioglitazone;in combination with insulin (i. trīskāršās kombinācijas terapija), kā palīglīdzekli, lai diētu un vingrinājumiem, lai uzlabotu glycaemic kontroles pacientiem, ja insulīna ir stabili devu un metformīns vien nenodrošina pietiekamu kontroles glycaemic.

Febuxostat Mylan Eiropas Savienība - latviešu - EMA (European Medicines Agency)

febuxostat mylan

mylan pharmaceuticals limited - febuxostat - hyperuricemia; arthritis, gouty; gout - antigut preparāti - febuxostat mylan indicēts profilaksi un ārstēšanu pieaugušiem pacientiem veikta ķīmijterapija haematologic malignancies starpproduktu ar augsta riska audzēju līzes sindroms (tls) hyperuricaemia. febuxostat mylan ir indicēts, lai ārstētu hronisku hyperuricaemia apstākļos, kad urate uzklāšanas jau ir noticis (tai skaitā vēsturē, vai klātbūtne, tophus un/vai podagras artrīta). febuxostat mylan ir norādīts pieaugušie.

Eucreas Eiropas Savienība - latviešu - EMA (European Medicines Agency)

eucreas

novartis europharm limited - vildagliptin, metformīns hidrohlorīds - cukura diabēts, 2. tips - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Eiropas Savienība - latviešu - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptin, metformīns hidrohlorīds - cukura diabēts, 2. tips - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 un 5. 1 pieejamo datu par dažādām kombinācijām).

Ariadne 125 mikrogrami/30 mikrogrami apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

ariadne 125 mikrogrami/30 mikrogrami apvalkotās tabletes

gedeon richter plc., hungary - levonorgestrelum, ethinylestradiolum - apvalkotās tabletes - 125 μg/30 μg

Logest 75 mikrogramu/20 mikrogramu apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

logest 75 mikrogramu/20 mikrogramu apvalkotās tabletes

bayer ag, germany - ethinylestradiolum, gestodenum - apvalkotā tablete - 75 μg/20 μg

Femoden 75/30 mikrogramu apvalkotās tabletes Latvija - latviešu - Zāļu valsts aģentūra

femoden 75/30 mikrogramu apvalkotās tabletes

bayer ag, germany - gestodenum, ethinylestradiolum - apvalkotās tabletes - 75 μg/30 μg