Европейски съюз - български - EMA (European Medicines Agency)

janssen-cilag international nv - канаглифлозина, метформина хидрохлорид - Захарен диабет тип 2 - Лекарства, използвани при диабет - vokanamet е показан при възрастни на възраст 18 и повече години с диабет тип 2, като допълнение към диета и физически упражнения за подобряване на гликемичния контрол при пациенти не се контролира адекватно за тяхното максимално переносимой дозата на метформина alonein на пациентите за максимално переносимой дозата на метформина заедно с други на глюкозата, намалява лекарства, включително инсулин, когато те не осигуряват адекватен гликемичен контрол. при пациенти вече лекувани с комбинация канаглифлозина и метформина като отделни tabletsfor резултатите от проучването по отношение на комбинирана терапия, влияние върху гликемичния контрол и сърдечно-съдови събития, както в добре проучените групи, вижте раздели 4. 4, 4. 5 и 5.

Европейски съюз - български - EMA (European Medicines Agency)

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.

Европейски съюз - български - EMA (European Medicines Agency)

virbac s.a. - жив атенюиран вирус на бяс, щам sag2 - Живи вирусни ваксини - raccoon dogs (nyctereutes procyonoides); red foxes (vulpes vulpes) - За активна имунизация на червени лисици и кучета миещи мечки за предотвратяване на инфекция от вируса на бяс. Продължителността на защитата е най-малко 6 месеца.

Европейски съюз - български - EMA (European Medicines Agency)

merck sharp & dohme b.v. - Пембролизумаб - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - Антинеопластични средства - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. Пациенти с egfr или АЛК положителни тумори мутации също трябва да получават таргетную терапия до получаване на Кейтруда. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

България - български - БАБХ (Българска агенция по безопасност на храните)

boehringer ingelheim animal health france scs - На вируса на нюкасълска болест, жива, щам на galq/ха-avinew - ефервесцентна таблетка; лиофилизирана таблетка - най-малко 5,5 log на 10 степен eid50 - птици, пуйки

България - български - БАБХ (Българска агенция по безопасност на храните)

fatro s.p.a - Вируса на болестта на Марек, щам ХВТ-126 - лиофилизат и разтворител за инжекционен разтвор - мин. 1500 pfu/ доза - пилета

България - български - БАБХ (Българска агенция по безопасност на храните)

boehringer ingelheim animal health france scs - Жив вирус на нюкасълска болест ТНА/дка avinew прецедете - замразена суспензия за пулверизиране - 5.5 до 6.7 log10 eid50 - пилета

България - български - БАБХ (Българска агенция по безопасност на храните)

intervet international b.v. - Вирус е инфекциозно бурсальной болест (ibdv), на живо, щам d78 - таблетка - ≥ 4,0 log 10 tcid50 - пилета

България - български - БАБХ (Българска агенция по безопасност на храните)

intervet international b.v - 6/85 галисептикум микоплазма мг - таблетка - ≥ 10 на степен 6,9 cfu - пилета

България - български - БАБХ (Българска агенция по безопасност на храните)

intervet international b.v - synoviae микоплазма, жив щам на МС1 - лиофилизат за суспензия - ≥ 10 на степен 6,5 и ≤ 10 на степен 8,0 cfu - пилета