Stayveer Европейски съюз - български - EMA (European Medicines Agency)

stayveer

janssen-cilag international nv - bosentan (as monohydrate) - hypertension, pulmonary; scleroderma, systemic - Други антихипертензивни средства - Лечение на пулмонална артериална хипертония (pah) за подобряване на физическия капацитет и симптоми при пациенти със Световната здравна организация (СЗО) функционален клас ІІІ. Ефективността е демонстрирана в:начална (идиопатическая и наследствена) уф;уф вторична склеродермии без значително интерстициална белодробна болест;ЛАГ, свързана с вродени системно-белодробни шънтове и физиология на eisenmenger. Някои подобрения са също така е показано при пациенти с ЛАГ, които функционален клас ii. stayveer също отбеляза спад в броя на новите дигиталната язви при пациенти със системна склеродермией и постоянна цифрова язвена болест.

PROCAPEN 300 mg/ml, Suspension for injection for cattle, pigs and horses 300 mg/ml България - български - БАБХ (Българска агенция по безопасност на храните)

procapen 300 mg/ml, suspension for injection for cattle, pigs and horses 300 mg/ml

animedica gmbh - benzylpenicillin, procain monohydrate - инжекционна суспензия - 300 mg/ml - говеда, коне, прасета

TANEVEN 300 mg/ml suspension for injection for horses, cattle, sheep, goats, dogs and cats 300 mg/ml България - български - БАБХ (Българска агенция по безопасност на храните)

taneven 300 mg/ml suspension for injection for horses, cattle, sheep, goats, dogs and cats 300 mg/ml

wdt- wirtschaftsgenossenschaft deutscher tierärzte eg - benzylpenicillin (procaine) monohydrate - Суспензия за инжектиране - 300 mg/ml - говеда, кози, коне, котки, кучета, овце

Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka) Европейски съюз - български - EMA (European Medicines Agency)

lenalidomide krka d.d. novo mesto (previously lenalidomide krka)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - Имуносупресори - multiple myelomalenalidomide krka d. novo mesto as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) е показан за лечение на възрастни пациенти с по-рано нелекувана множествена миеломой, на които не се разчита за трансплантация. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka d. novo mesto as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) е показан за лечение на възрастни пациенти с по-рано нелекувана множествена миеломой, на които не се разчита за трансплантация. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Европейски съюз - български - EMA (European Medicines Agency)

lenalidomide krka (previously lenalidomide krka d.d. novo mesto)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - Имуносупресори - multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) е показан за лечение на възрастни пациенти с по-рано нелекувана множествена миеломой, на които не се разчита за трансплантация. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 и 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) е показан за лечение на възрастни пациенти с по-рано нелекувана множествена миеломой, на които не се разчита за трансплантация. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 и 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Sitagliptin / Metformin hydrochloride Mylan Европейски съюз - български - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - Захарен диабет тип 2 - Лекарства, използвани при диабет - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan 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 mylan 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. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan 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.

АНАЛГИН БИОФАРМ 30% инжекционен разтвор 300 mg/ml България - български - БАБХ (Българска агенция по безопасност на храните)

АНАЛГИН БИОФАРМ 30% инжекционен разтвор 300 mg/ml

„БИОФАРМ ИНЖЕНЕРИНГ“ АД - metamizole sodium monohydrate - инжекционен разтвор - 300 mg/ml - говеда, коне, кучета, морски свинчета

Purevax FeLV Европейски съюз - български - EMA (European Medicines Agency)

purevax felv

boehringer ingelheim vetmedica gmbh - вирус котешка левкемия рекомбинантен на канарчетата (vcp97) - Имуномодулатори за котки,на - Котки - Активна имунизация на котки на възраст 8 седмици или повече срещу котешка левкемия за профилактика на персистираща виремия и клинични признаци на свързаното заболяване. Началото на имунитета е доказано 2 седмици след първоначалния ваксинационен курс. Продължителността на имунитета е една година след последната ваксинация.