Irbesartan Hydrochlorothiazide BMS Uni Eropa - Bulgar - EMA (European Medicines Agency)

irbesartan hydrochlorothiazide bms

bristol-myers squibb pharma eeig - Ирбесартан, гидрохлортиазид - Хипертония - Агенти, действащи върху системата ренин-ангиотензин - Лечение на есенциална хипертония. Това е комбинация от фиксирани дози е показана при възрастни пациенти, при които кръвното налягане не е достатъчно контролирано ирбесартаном или гидрохлоротиазидом сам (виж раздел 5.

Eucreas Uni Eropa - Bulgar - EMA (European Medicines Agency)

eucreas

novartis europharm limited - вилдаглиптин, метформин хидрохлорид - Захарен диабет тип 2 - 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) Uni Eropa - Bulgar - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - вилдаглиптин, метформин хидрохлорид - Захарен диабет тип 2 - 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 и 5. 1 за наличните данни за различни комбинации).

Imprida Uni Eropa - Bulgar - EMA (European Medicines Agency)

imprida

novartis europharm ltd - valsartan, amlodipine (as amlodipine besilate) - Хипертония - Агенти, действащи върху системата ренин-ангиотензин - Лечение на есенциална хипертония. imprida е показан при пациенти, при които кръвното налягане не е достатъчно контролирано на Амлодипин или валсартан под формата на монотерапии.

Hiprabovis IBR Marker Live Uni Eropa - Bulgar - EMA (European Medicines Agency)

hiprabovis ibr marker live

laboratorios hipra s.a - жив ge-tk- двойно-ген-делящ говежди херпес вирус тип 1, щам ceddel: 106.3-107.3 ccid50 - Имунологични - Говеда - За активна имунизация на едър рогат добитък, с три месечна възраст на едър рогат добитък срещу вируса на херпес симплекс тип 1 (bohv-1) за намаляване на клинични признаци на инфекциозно котешки ринотрахеит едър рогат добитък (idb) и областта на отделяне на вируса. Началото на имунитета: 21 дни след завършване на основната схема на ваксинация. Продължителност на имунитета: 6 месеца след завършване на основната схема за ваксинация.

Virbagen Omega Uni Eropa - Bulgar - EMA (European Medicines Agency)

virbagen omega

virbac s.a. - рекомбинантен омега интерферон от котешки произход - Иммуностимуляторы, - dogs; cats - dogsreduction of mortality and clinical signs of parvovirosis (enteric form) in dogs from one month of age. catstreatment of cats infected with feline leukaemia virus (felv) and / or feline immunodeficiency virus (fiv), in non-terminal clinical stages, from the age of nine weeks. in a field study conducted, it was observed that there was:a reduction of clinical signs during the symptomatic phase (four months);a reduction of mortality:in anaemic cats, mortality rate of about 60% at four, six, nine and 12 months was reduced by approximately 30% following treatment with interferon;in non-anaemic cats, mortality rate of 50% in cats infected by felv was reduced by 20% following treatment with interferon. При котки, заразени с fiv, смъртността е ниска (5%) и не е повлияна от лечението.

Zomarist Uni Eropa - Bulgar - EMA (European Medicines Agency)

zomarist

novartis europharm limited  - вилдаглиптин, метформин хидрохлорид - Захарен диабет тип 2 - Лекарства, използвани при диабет - zomarist 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.

Segluromet Uni Eropa - Bulgar - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - Захарен диабет тип 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Enhertu Uni Eropa - Bulgar - EMA (European Medicines Agency)

enhertu

daiichi sankyo europe gmbh - trastuzumab deruxtecan - Неоплазми на гърдата - Антинеопластични средства - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Enteroporc Coli AC Uni Eropa - Bulgar - EMA (European Medicines Agency)

enteroporc coli ac

ceva santé animale - clostridium perfringens type c, beta1 toxoid / clostridium perfringens, type a, alpha toxoid / clostridium perfringens, type a, beta2 toxoid / escherichia coli, fimbrial adhesin f4ab / escherichia coli, fimbrial adhesin f4ac / escherichia coli, fimbrial adhesin f5 / escherichia coli, fimbrial adhesin f6 - immunologicals for suidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) escherichia + clostridium - Прасета - for the passive immunisation of progeny by active immunisation of pregnant sows and gilts to reduce:-           clinical signs (severe diarrhoea) and mortality caused by escherichia coli strains expressing the fimbrial adhesins f4ab, f4ac, f5 and f6-           clinical signs (diarrhoea during the first days of life) associated with clostridium perfringens type a expressing alpha and beta 2 toxins-           clinical signs and mortality associated with haemorrhagic and necrotising enteritis caused by clostridium perfringens type c expressing beta1 toxin.