Evropska unija - bolgarščina - EMA (European Medicines Agency)

sanofi pasteur europe - filamentous haemagglutinin, haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate), hepatitis b surface antigen, pertussis toxoid, poliovirus (inactivated) type 1 (mahoney strain) produced on vero cells, poliovirus (inactivated) type 2 (mef-1 strain) produced on vero cells, poliovirus (inactivated) type 3 (saukett strain) produced on vero cells, tetanus protein, tetanus toxoid adsorbed on aluminium hydroxide, hydrated, diphtheria toxoid - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - Ваксини - hexyon (dtap / ipv-hb-hib) е показан за началното и помощник ваксинация на кърмачета и малки деца от шестседмична възраст срещу дифтерия, тетанус, коклюш, хепатит Б, полиомиелит и инвазивни заболявания, причинени от haemophilus инфлуенца тип б (hib). Използването на тази ваксина трябва да бъде приложена в съответствие с официалните препоръки.

Evropska unija - bolgarščina - 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.

Evropska unija - bolgarščina - EMA (European Medicines Agency)

pfizer europe ma eeig - neisseria meningitidis серогрупа В fhbp (рекомбинантен липидиран fhbp (фактор Н свързващ протеин)) подсемейство А; neisseria meningitidis серогрупа В fhbp (рекомбинантен липидиран fhbp (фактор Н свързващ протеин)) подсемейство В - Менингит, менингококов - bacterial vaccines, meningococcal vaccines - trumenba е показан за активна имунизация на лица на 10 години и по-големи, за да се предотврати инвазивното менингококова болест, причинена от neisseria meningitidis серогрупа В. Използването на тази ваксина трябва да бъде приложена в съответствие с официалните препоръки.

Evropska unija - bolgarščina - EMA (European Medicines Agency)

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.

Evropska unija - bolgarščina - EMA (European Medicines Agency)

dynavax gmbh - повърхностен антиген на хепатит В - Хепатит Б - Ваксини - heplisav b is indicated for the active immunisation against hepatitis b virus infection (hbv) caused by all known subtypes of hepatitis b virus in adults 18 years of age and older. the use of heplisav b should be in accordance with official recommendations. it can be expected that hepatitis d will also be prevented by immunisation with heplisav b as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection.

Evropska unija - bolgarščina - EMA (European Medicines Agency)

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - Денга - Ваксини - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

Evropska unija - bolgarščina - EMA (European Medicines Agency)

almirall s.a - tildrakizumab - псориазис - Иммунодепрессанты, инхибитори на интерлевкин, - ilumetri е показан за лечение на възрастни пациенти с умерена до тежка форма на плака псориазис, които са кандидати за системната терапия.

Evropska unija - bolgarščina - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.