Den europeiske union - latvisk - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - maribavir - citomegalovīrusu infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). jāņem vērā oficiālās vadlīnijas par piemērotu izmantot pretvīrusu aģentu.

Den europeiske union - latvisk - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - cukura diabēts, 2. tips - cukura diabēts - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride sun is indicated in combination with a sulphonylurea (i. , triple kombinēto terapiju), kā palīglīdzekli, lai diētu un vingrošanu pacientiem nepietiekami kontrolē par to maksimālā pieļaujama devu metformīns un sulfonilurīnvielas pamata. sitagliptin/metformin hydrochloride sun is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. sitagliptin/metformin hydrochloride sun is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Den europeiske union - latvisk - EMA (European Medicines Agency)

teva b.v. - clopidogrel (as hydrogen sulfate) - myocardial infarction; acute coronary syndrome; peripheral vascular diseases; stroke - antitrombotiskie līdzekļi - secondary prevention of atherothrombotic events clopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. pieaugušo pacientu, kas slimo ar akūtu koronāro sindromu:bez st segmenta pacēluma akūtu koronāro sindromu (nestabila stenokardija vai ne-q zoba miokarda infarkts), tostarp pacientiem, kam veic stentu izvietošana pēc perkutānas koronāras intervences, kombinācijā ar acetilsalicilskābi (asa). st segmenta pacēlums, akūts miokarda infarkts, kopā ar asa, medicīniski ārstēti pacienti saņemt trombolītiskā terapija. profilakse atherothrombotic un trombembolisku notikumu ātriju fibrillationin pieaugušiem pacientiem ar priekškambaru mirdzēšana, kuriem ir vismaz viena riska faktors asinsvadu notikumi, nav piemēroti apstrādei ar vitamīna k antagonisti (vka) un, kas ir zems asiņošanas risku, klopidogrelu, ir norādīts kopā ar asa novēršanas atherothrombotic un trombembolisku notikumu, tostarp insulta.

Den europeiske union - latvisk - EMA (European Medicines Agency)

astrazeneca ab - dapagliflozin propāndiols monohidrāts - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - cukura diabēts - type 2 diabetes mellitusedistride is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. papildus citām zālēm, lai ārstētu 2. tipa cukura diabētu. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 un 5. heart failureedistride is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseedistride is indicated in adults for the treatment of chronic kidney disease.

Den europeiske union - latvisk - EMA (European Medicines Agency)

mylan pharmaceuticals limited - emtricitabine, tenofovir disoproxil maleāts - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - treatment of hiv-1 infection:emtricitabine/tenofovir disoproxil mylan is indicated in antiretroviral combination therapy for the treatment of hiv-1 infected adults (see section 5. emtricitabine/tenofovir disoproxil mylan is also indicated for the treatment of hiv-1 infected adolescents, with nrti resistance or toxicities precluding the use of first line agents, (see sections 4. 2, 4. 4 un 5. pre-exposure prophylaxis (prep):emtricitabine/tenofovir disoproxil mylan is indicated in combination with safer sex practices for pre-exposure prophylaxis to reduce the risk of sexually acquired hiv-1 infection in adults and adolescents at high risk (see sections 4. 2, 4. 4 un 5.

Den europeiske union - latvisk - EMA (European Medicines Agency)

astrazeneca ab - dapagliflozin propāndiols monohidrāts - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - cukura diabēts - type 2 diabetes mellitusforxiga is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. papildus citām zālēm, lai ārstētu 2. tipa cukura diabētu. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 un 5. heart failureforxiga is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseforxiga is indicated in adults for the treatment of chronic kidney disease.

Den europeiske union - latvisk - EMA (European Medicines Agency)

gilead sciences ireland uc - ledipasvir, sofosbuvir - c hepatīts, hronisks - pretvīrusu līdzekļi sistēmiskai lietošanai - harvoni is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 un 5. hepatīta c vīrusa (hcv) genotipa-īpašas darbības, skatīt 4. 4 un 5.

Den europeiske union - latvisk - EMA (European Medicines Agency)

zoetis belgium sa - oklatzībīna maleāts - agents for dermatitis, excluding corticosteroids - suņi - - treatment of pruritus associated with allergic dermatitis in dogs. - treatment of clinical manifestations of atopic dermatitis in dogs.

Den europeiske union - latvisk - EMA (European Medicines Agency)

novartis europharm limited - trametinib - melanoma - antineoplastiski līdzekļi - melanomatrametinib as monotherapy or in combination with dabrafenib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 un 5. trametinib monotherapy has not demonstrated clinical activity in patients who have progressed on a prior braf inhibitor therapy (see section 5. adjuvant treatment of melanomatrametinib in combination with dabrafenib is indicated for the adjuvant treatment of adult patients with stage iii melanoma with a braf v600 mutation, following complete resection. nav maza šūnu plaušu vēzis (nsclc)trametinib kopā ar dabrafenib ir norādīts ārstēšanai pieaugušiem pacientiem ar progresējošu ne-maza šūnu plaušu vēzis ar braf v600 mutācijas.

Den europeiske union - latvisk - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - lamivudine - b hepatīts, hronisks - pretvīrusu līdzekļi sistēmiskai lietošanai - zeffix is indicated for the treatment of chronic hepatitis b in adults with: , compensated liver disease with evidence of active viral replication, persistently elevated serum alanine aminotransferase (alt) levels and histological evidence of active liver inflammation and / or fibrosis. uzsākšanas lamivudīnu ārstēšanai, jāapsver tikai tad, kad izmantot alternatīvu pretvīrusu līdzeklis ar augstāku ģenētisko barjeru nav pieejami, vai arī ir nepieciešams;, decompensated aknu slimība kopā ar otro aģents, bez krusteniskās rezistences pret lamivudīnu.