FIPNIL COMBO 50mg/60mg разтвор за прилагане върху ограничен участък за котки и фретки 50mg; 60mg България - български - БАБХ (Българска агенция по безопасност на храните)

fipnil combo 50mg/60mg разтвор за прилагане върху ограничен участък за котки и фретки 50mg; 60mg

chanelle pharmaceuticals manufacturing ltd. - фипронил; (с)-метопрен - разтвор за прилагане върху ограничен участък - 50mg; 60mg - котки, порове

FIPNIL COMBO 67mg/60.3mg разтвор за прилагане върху ограничен участък за дребни кучета 67mg; 60,30 mg България - български - БАБХ (Българска агенция по безопасност на храните)

fipnil combo 67mg/60.3mg разтвор за прилагане върху ограничен участък за дребни кучета 67mg; 60,30 mg

chanelle pharmaceuticals manufacturing ltd - фипронил; (с)-метопрен - разтвор за прилагане върху ограничен участък - 67mg; 60,30 mg - кучета

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

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - Ваксини - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. Използването на тази ваксина трябва да бъде приложена в съответствие с официалните препоръки.

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

tecfidera

biogen netherlands b.v. - диметил фумарат - Множествена склероза - Имуносупресори - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

PARVOSUIN MR,AD България - български - БАБХ (Българска агенция по безопасност на храните)

parvosuin mr,ad

laboratorios hipra, s.a. - aujeszky, с вирусно заболяване, Инак. напрежение ets отрицателни Барт k61; парвовирус прасета, Инак., НАДЛ щам - 2; Эризипелотриксов rhusiopathiae, Инак., щам r32e11 - инжекционна емулсия - ≥ 10 на 7, 5 степен tcid50; ≥ 2048 uha; ≥ 2 x 10 на 10 степен cfu - свине

PORCILIS ERY PARVO LEPTO SUSPENSION FOR INJECTION FOR PIGS България - български - БАБХ (Българска агенция по безопасност на храните)

porcilis ery parvo lepto suspension for injection for pigs

intervet international b.v. - erysipelotrix rhusiopathiae, серотип 2, щам м2; парвовирус прасета щам 014, лептоспир interrogans, Тянитолкая серогруппы, серовара Портланд-Вэ,щам sa-12-000; виж ccc - инжекционна суспензия - ≥1ppd на 1 степен; ≥ 130 u на 2 степен; ≥ 2816 u на 2 степен; ≥210 u на 2 степен; ≥ 1704 u на 2 степен; ≥ 648 u на 2 степен; ≥ 1 - прасета

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

skysona

bluebird bio (netherlands) b.v. - elivaldogene autotemcel - adrenoleukodystrophy - Други лекарства в нервната система - treatment of early cerebral adrenoleukodystrophy in patients less than 18 years of age, with an abcd1 genetic mutation, and for whom a human leukocyte antigen (hla) matched sibling haematopoietic stem cell donor is not available.

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

vumerity

biogen netherlands b.v. - diroximel fumarate (biib098) - Множествена Склероза, Рецидивно-Ремиттирующее - Имуносупресори - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).