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

purevax rcpch felv

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97), attenuated chlamydophila felis (905 strain) - Имуномодулатори за котки,на - Котки - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against chlamydophila felis infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus, chlamydophila felis and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the chlamydiosis and feline leukaemia components, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

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

proquad

merck sharp & dohme b.v. - вирус, живи атенюирани, морбили, вируси, живи атенюирани, паротит, вирус, живи атенюирани, рубеола, вируси, живи атенюирани, варицела - chickenpox; rubella; measles; mumps; immunization - Ваксини - proquad е показан за едновременна ваксинация срещу морбили, паротит, рубеола и варицела при лица на възраст от 12 месеца. proquad може да се предписват на лица с 9-месечна възраст при наличието на особени обстоятелства (e. в съответствие с Националния календар за ваксинация, ситуации светкавица, или пътуване в регион с висока заболеваемостта корью.

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

gumbohatch

laboratorios hipra, s.a. - да живее аттенуированного вируса заразно бурсальной болест (ibdv), прецедете 1052 - Имуномодулатори за птици, домашни животни, живи вирусни ваксини, птици заразно бурсальной на заболяването е вирус (болест на Гамборо) - chicken; embryonated chicken eggs - За активна имунизация на 1-дневни пилета и ембриони пилета-бройлери яйца за намаляване на клиничните прояви и загубата фабрициевой чанта, причинени от много вирулентные птици заразно бурсальной болестта вирусна инфекция.

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

vaxchora

bavarian nordic a/s - холерный вибрион, щам и ИЗРАВНИТЕЛНИТЕ 103-hgr за да живеят - холера - Ваксини - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. Тази ваксина трябва да се използва в съответствие с официалните препоръки.

Fluad Tetra Европейски съюз - български - EMA (European Medicines Agency)

fluad tetra

seqirus netherlands b.v. - a/darwin/9/2021 (h3n2) - like strain (a/darwin/6/2021, ivr-227) / a/victoria/4897/2022 (h1n1) pdm09-like strain (a/victoria/4897/2022, ivr-238) / b/phuket/3073/2013-like strain (b/phuket/3073/2013, bvr-1b) / influenza virus b/austria/1359417/2021-like strain (b/austria/1359417/2021, bvr-26) - Грип, Човек - Ваксини - Профилактика на грип при хора в напреднала възраст (65 години и повече). fluad Тетра трябва да се прилага в съответствие с официалните препоръки.

Vectormune FP ILT Европейски съюз - български - EMA (European Medicines Agency)

vectormune fp ilt

ceva-phylaxia co. ltd. - recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus, live - Пиле - for active immunisation of chickens from 8 weeks of age in order to reduce the skin lesions due to fowlpox and to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis.

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

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

BIOBOS Respi 5 Plus lyophilisate and suspension for suspension  for injection България - български - БАБХ (Българска агенция по безопасност на храните)

biobos respi 5 plus lyophilisate and suspension for suspension for injection

„Лекоом“ АД - lyophilisate - live attenuated bovine herpesvirus type 1 (bhv-1), strain bio 27 : ibr ge-negative; suspension – bovine respiratory syncytial virus (brsv) inactivated, strain bio 24; bovine parainfluenza 3 virus (pi3v) inactivated, strain bio 23; bovine viral diarrhoea virus (bvdb) inactivated, strain bio 25; manheimia (pasteurella) hemolytica, inactivated, strain dsm 5283, serotype А1 - инжекционна суспензия - 105.7-107.5 tcid50/ 2ml; rp ≥ 1/ 2ml - говеда

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

tyenne

fresenius kabi deutschland gmbh - тоцилизумаб - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - Имуносупресори - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

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

avinew neo

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