Европейски съюз - български - EMA (European Medicines Agency)

laboratorios hipra, s.a. - Эймери acervulina, прецедете 003, Эймери Максим, се прецежда 013, Эймери митис, прецедете 006, Эймери ргаесох, прецедете 007, Эймери tenella, прецедете 004 - Да живее паразитные ваксина, имуномодулатори за птици - Пиле - За активна имунизация на пилета от 1 ден на възрастта за намаляване на лезии на червата ооцисти са и изход, свързани с кокцидиоза, причинени от Эймери acervulina, Эймери Максим, Эймери митис, Эймери ргаесох и Эймери tenella и намаляване на клиничните прояви (диария), свързани с Эймери acervulina, Эймери Максим и Эймери tenella.

Европейски съюз - български - EMA (European Medicines Agency)

laboratorios hipra, s.a. - ваксина срещу кокцидиоза при пилета - Да живее паразитные ваксина, имуномодулатори за птици - Пиле - За активна имунизация на пилета от 1 ден на възрастта за намаляване на клиничните прояви (диария), лезии на червата ооцисти са и изход, свързани с кокцидиоза, причинени от Эймери acervulina, Эймери брунетти, Эймери Максим, Эймери necatrix и Эймери tenella.

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

intervet international b.v. - Эймери acervulina с. л., Эймери Брунетти с. л., Эймери Максим церебрална парализа, Эймери Максим mfp, Эймери митис с. л., Эймери necatrix с. л., Эймери ргаесох с. л., Эймери tenella с. л. - перорална суспензия - 500/0,1 ml; 100/0,1 ml; 200/0,1 ml; 100/0,1 ml; 1000/0,1 ml; 500/0,1 ml; 100/0,1 ml; 500/0,1 ml - пилета

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

laboratorios hipra, s.a. - Эймери acervulina, прецедете 003; Эймери acervulina, прецедете 013; Эймери митис, прецедете 006; Эймери ргаесох, прецедете 007; Эймери tenella, прецедете 004 - перорална суспензия - Всяка доза (0.007 ml) съдържа 300-390 кокцидир; 200-260/кокцидии; 300-390/кокцидии; 300-390/кокцидии; 250-325/ кокцидии - бройлери, пилета

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

biopharm - Эймери acervulina, Эймери Максим, Эймери tenella, Эймери necatrix в 1% w/в-тия воден разтвор на хлорамин Б - перорална суспензия - 30 000 - 50 000 броя спорулирали ооцисти от атенуирани линии кокцидии на eimeria aсervulina, eimeria maxima and eimeria tenella - птици

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

biopharm - Эймери acervulina, Эймери Максим, Эймери tenella в 1% w/в-тия воден разтвор на хлорамин Б - перорална суспензия - 30 000 - 50 000 броя спорулирали ооцисти от атенуирани линии кокцидии - пилета, птици

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

Биовет АД - Эймери acervulina (щам РА|3+20 ), Эймери Максим (щам gmt+10), Эймери Максим (щам gmt+10), Эймери Максим (щам gmt+10) - перорална суспензия - 50-139 ооцисти; 100-278 ооцисти; 100-278 ооцисти; 150-417 ооцисти - кокошки

Европейски съюз - български - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; mesothelioma; colorectal neoplasms - Антинеопластични средства - melanomaopdivo as monotherapy or in combination with ipilimumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older. relative to nivolumab monotherapy, an increase in progression free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression. adjuvant treatment of melanomaopdivo as monotherapy is indicated for the adjuvant treatment of adults and adolescents 12 years of age and older with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection. non-small cell lung cancer (nsclc)opdivo in combination with ipilimumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. opdivo as monotherapy is indicated for the treatment of locally advanced or metastatic non-small cell lung cancer after prior chemotherapy in adults. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. malignant pleural mesothelioma (mpm)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. neoadjuvant treatment of nsclcopdivo in combination with platinum-based chemotherapy is indicated for the neoadjuvant treatment of resectable non-small cell lung cancer at high risk of recurrence in adult patients whose tumours have pd-l1 expression ≥ 1%. renal cell carcinoma (rcc)opdivo as monotherapy is indicated for the treatment of advanced renal cell carcinoma after prior therapy in adults. opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with intermediate/poor risk advanced renal cell carcinoma. opdivo in combination with cabozantinib is indicated for the first-line treatment of adult patients with advanced renal cell carcinoma. classical hodgkin lymphoma (chl)opdivo as monotherapy is indicated for the treatment of adult patients with relapsed or refractory classical hodgkin lymphoma after autologous stem cell transplant (asct) and treatment with brentuximab vedotin. squamous cell cancer of the head and neck (scchn)opdivo as monotherapy is indicated for the treatment of recurrent or metastatic squamous cell cancer of the head and neck in adults progressing on or after platinum based therapy. urothelial carcinomaopdivo as monotherapy is indicated for the treatment of locally advanced unresectable or metastatic urothelial carcinoma in adults after failure of prior platinum containing therapy. adjuvant treatment of urothelial carcinomaopdivo as monotherapy is indicated for the adjuvant treatment of adults with muscle invasive urothelial carcinoma (miuc) with tumour cell pd-l1 expression ≥ 1%, who are at high risk of recurrence after undergoing radical resection of miuc. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)opdivo in combination with ipilimumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy. oesophageal squamous cell carcinoma (oscc)opdivo in combination with ipilimumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%. opdivo as monotherapy is indicated for the treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma after prior fluoropyrimidine- and platinum-based combination chemotherapy. adjuvant treatment of oesophageal or gastro-oesophageal junction cancer (oc or gejc)opdivo as monotherapy is indicated for the adjuvant treatment of adult patients with oesophageal or gastro-oesophageal junction cancer who have residual pathologic disease following prior neoadjuvant chemoradiotherapy. gastric, gastro‑oesophageal junction (gej) or oesophageal adenocarcinomaopdivo in combination with fluoropyrimidine- and platinum-based combination chemotherapy is indicated for the first‑line treatment of adult patients with her2‑negative advanced or metastatic gastric, gastro‑oesophageal junction or oesophageal adenocarcinoma whose tumours express pd-l1 with a combined positive score (cps) ≥ 5.

Европейски съюз - български - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - diphtheria toxoid, hepatitis b surface antigen, bordetella pertussis (inactivated), tetanus toxoid - hepatitis b; tetanus; immunization; whooping cough; diphtheria - Ваксини - tritanrix hepb е показан за активна имунизация срещу дифтерия, тетанус, коклюш и хепатит b (hbv) при кърмачета от шест седмици насам (виж точка 4.

Европейски съюз - български - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin), poliovirus (inactivated) (type 1 (mahoney strain), type 2 (mef-1 strain), type 3 (saukett strain)), hepatitis b surface antigen - hepatitis b; tetanus; immunization; whooping cough; poliomyelitis; diphtheria - Ваксини - infanrix penta е показан за първична и бустер ваксинация на кърмачета срещу дифтерия, тетанус, коклюш, хепатит В и полиомиелит.