Rivaroxaban Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

rivaroxaban accord

accord healthcare s.l.u. - ривароксабан - acute coronary syndrome; coronary artery disease; peripheral arterial disease; venous thromboembolism; stroke; atrial fibrillation; pulmonary embolism - Антитромботични агенти - Предотвратяване на венозна тромбоемболия (ВТЕ) при възрастни пациенти, подложени на елективна операция за замяна на тазобедрена или колянна става. Лечение на дълбока венозна тромбоза (dvt) и тромбоэмболии белодробната артерия (ТЭЛА) и за превенция на рецидив на дълбока венозна тромбоза и ТЭЛА при възрастни. (see section 4. 4 for haemodynamically unstable pe patients. Лечение на дълбока венозна тромбоза (dvt) и тромбоэмболии белодробната артерия (ТЭЛА) и за превенция на рецидив на дълбока венозна тромбоза и ТЭЛА при възрастни. (see section 4. 4 за гемодинамически нестабилна ТЭЛА пациенти). adultsprevention of stroke and systemic embolism in adult patients with non valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. Лечение на дълбока венозна тромбоза (dvt) и тромбоэмболии белодробната артерия (ТЭЛА) и за превенция на рецидив на дълбока венозна тромбоза и ТЭЛА при възрастни. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. rivaroxaban accord, co administered with acetylsalicylic acid (asa) alone or with asa plus ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers (see sections 4. 3, 4. 4 и 5. rivaroxaban accord, co administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events. adultsprevention of stroke and systemic embolism in adult patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. Лечение на дълбока венозна тромбоза (dvt) и тромбоэмболии белодробната артерия (ТЭЛА) и за превенция на рецидив на дълбока венозна тромбоза и ТЭЛА при възрастни. (see section 4. 4 for haemodynamically unstable pe patients. )paediatric populationtreatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Sitagliptin Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

sitagliptin accord

accord healthcare s.l.u. - sitagliptin hydrochloride - Захарен диабет тип 2 - Лекарства, използвани при диабет - for adult patients with type 2 diabetes mellitus, sitagliptin accord is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (ppary) agonist (i. a thiazolidinedione) when use of a ppary agonist is appropriate and when diet and exercise plus the ppary agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a ppary agonist and metformin when use of a ppary agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin accord is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

Sitagliptin / Metformin hydrochloride Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride accord

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - Захарен диабет тип 2 - Лекарства, използвани при диабет - for adult patients with type 2 diabetes mellitus:it 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. it is indicated in combination with a sulphonylurea (i. тройно комбинирано лечение) като допълнение към диета и упражнения при пациенти, недостатъчно контролирани за тяхното максимално переносимой дозата на метформина и сульфонилмочевины. it 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. it 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.

Tolvaptan Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

tolvaptan accord

accord healthcare s.l.u. - Толваптан - Неподходящ синдром на adh - Диуретици, - tolvaptan is indicated in adults for the treatment of hyponatremia secondary to the syndrome of inappropriate antidiuretic hormone secretion (siadh).

Sunitinib Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

sunitinib accord

accord healthcare s.l.u. - сунитиниб - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - Антинеопластични средства - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

Icatibant Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

icatibant accord

accord healthcare s.l.u. - icatibant acetate - Ангиоедем, наследствено - other hematological agents - icatibant accord is indicated for symptomatic treatment of acute attacks of hereditary angioedema (hae) in adults, adolescents and children aged 2 years and older, with c1 esterase inhibitor deficiency.

Teriflunomide Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

teriflunomide accord

accord healthcare s.l.u. - teriflunomide - Множествена Склероза, Рецидивно-Ремиттирующее - Иммунодепрессанты селективен иммунодепрессанты - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Eptifibatide Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

eptifibatide accord

accord healthcare s.l.u. - ептифибатид - Инфаркт на миокарда - Антитромботични агенти - Ептифибатид accord е предназначено за използване с Ацетилсалицилова киселина и unfractionated хепарин. Ламифибана Акорд е показан за профилактика на ранен инфаркт на миокарда при възрастни пациенти с нестабилна ангина и не-q-инфарктом на миокарда, с последния епизод на болка в гръдния кош възниква в рамките на 24 часа электрокардиограммой (ЕКГ), промени и/или повишени нива на кардиоспецифических ензими. Пациентите най-вероятно, за да се възползват от Ламифибана лечение съгласието на тези с висок риск от развитие на инфаркт на миокарда в рамките на първите 3-4 дни след появата на остри симптоми на ангина пекторис, включително, например, са тези, които могат да преминат в началото на ЧТКА (перкутанна Транслюминальная коронарна ангиопластика).

Pramipexole Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

pramipexole accord

accord healthcare s.l.u. - прамипексол дихидрохлорид монохидрат - parkinson disease; restless legs syndrome - Антипаркинсонови лекарства - pramipexole accord е показан при възрастни за лечение на признаците и симптомите на идиопатична болест на parkinson, самостоятелно (без леводопа) или в комбинация с леводопа, i. в течение на болестта чрез до късните стадии, когато ефектът на levodopa намалява или става непостоянен и флуктуации в терапевтичния ефект се появи (край-на-доза или "on-off" флуктуации).

Entecavir Accord Umoja wa Ulaya - Kibulgaria - EMA (European Medicines Agency)

entecavir accord

accord healthcare s.l.u. - Энтекавир - Хепатит В, хроничен - Антивирусни средства за системно приложение - entecavir accord is indicated for the treatment of chronic hepatitis b virus (hbv) infection in adults with: , compensated liver disease and evidence of active viral replication, persistently elevated serum alanine aminotransferase (alt) levels and histological evidence of active inflammation and/or fibrosis. , декомпенсированные заболявания на черния дроб . Като компенсированные и декомпенсированные заболявания на черния дроб, този индекс се базира на данни от клинични проучвания при наивни пациенти нуклеозидов с положителен резултат на теста за hbeag и hbeag-отрицателен hbv-инфекция. По отношение на пациентите с рефрактерен на ламивудин хепатит В. Энтекавир accord също така е показан за лечение на хронична hbv-инфекция в нуклеозидов наивен педиатрични пациенти от 2 до.