Forxiga الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

forxiga

astrazeneca ab - дадаглифлозин пропандиол монохидрат - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - Лекарства, използвани при диабет - 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. в допълнение към други лекарства за лечение на захарен диабет тип 2 . 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 и 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.

Tekturna الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

tekturna

novartis europharm ltd. - алискирен - Хипертония - Агенти, действащи върху системата ренин-ангиотензин - Лечение на есенциална хипертония.

Dapagliflozin Viatris الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

dapagliflozin viatris

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - Лекарства, използвани при диабет - type 2 diabetes mellitusdapagliflozin viatris 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 exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 diabetes. 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 и 5. heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Jardiance الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

jardiance

boehringer ingelheim international gmbh - empagliflozin - diabetes mellitus, type 2; heart failure; renal insufficiency, chronic - Лекарства, използвани при диабет - type 2 diabetes mellitusjardiance is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered in addition to other medicinal products for the treatment of diabetesfor study results with respect to combinations of therapies, effects on glycaemic control, and cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 и 5. of the annex. heart failurejardiance is indicated in adults for the treatment of symptomatic chronic heart failure.  chronic kidney diseasejardiance is indicated in adults for the treatment of chronic kidney disease.

Purevax RCP الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

purevax rcp

boehringer ingelheim vetmedica gmbh - attenuated feline panleucopenia virus (pli iv) - Имуномодулатори за котки,на - Котки - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs. onset of immunity is one week after primary vaccination course the duration of immunity is one year after the primary vaccination course and three years after the last re-vaccination.

Mekinist الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

mekinist

novartis europharm limited - trametinib - Меланомът - Антинеопластични средства - 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 и 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. Немелкоклеточный рак на белия дроб (НМРЛ)trametinib в комбинация с dabrafenib е показан за лечение на възрастни пациенти с предварително non-малките рак на белите дробове клетки с Браф v600 мутация далеч .

LysaKare الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

lysakare

advanced accelerator applications - l-arginine hydrochloride, l-lysine hydrochloride - Лъчева Щети - detoxifying agents for antineoplastic treatment - lysakare е показан за намаляване на излагането на радиация при бъбречна пептид-рецепторного радионуклидной терапия (prrt) с Лютеций (177lu) oxodotreotide при възрастни.

Mayzent الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

mayzent

novartis europharm limited  - siponimod фумаровая киселина - Множествена Склероза, Рецидивно-Ремиттирующее - Селективни имуносупресори - mayzent е показан за лечение на възрастни пациенти с втори-белег множествена склероза (ВПРС) с активно заболяване свидетелстват за рецидиви или функциите за визуализация на активност на възпалителния процес.

Bemrist Breezhaler الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

bemrist breezhaler

novartis europharm limited  - indacaterol, mometasone furoate - астма - Лекарства за обструктивна заболявания на дихателните пътища, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Fingolimod Mylan الاتحاد الأوروبي - البلغارية - EMA (European Medicines Agency)

fingolimod mylan

mylan ireland limited - финголимод хидрохлорид - Множествена Склероза, Рецидивно-Ремиттирующее - Имуносупресори - indicated as single disease modifying therapy in highly active relapsing remitting multiple sclerosis for the following groups of adult and paediatric patients aged 10 years and older:patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (for exceptions and information about washout periods see sections 4. 4 и 5. 1)orpatients с бързо се развива тежка relapsing начин множествена склероза се определя от 2 или по-тежки рецидиви в рамките на една година, и с 1 или по-гадолиний активизиране на огнища на ядрено-магнитен резонанс на главния мозък или значително увеличаване на натоварването Т2 лезии в сравнение с най-новите ядрено-магнитен резонанс.