Evropska unija - slovenščina - EMA (European Medicines Agency)

dynavax gmbh - površinski antigen hepatitisa b - hepatitis b - cepiva - 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.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

hospira uk ltd - ceftazidim - prašek za raztopino za injiciranje/infundiranje - ceftazidim 1000 mg / 1 viala - ceftazidim

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi pasteur - hepatitis b surface antigen, diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens pertussis toxoid filamentous haemagglutinin, poliovirus (inactivated) type 1 (mahoney) type 2 (mef-1) type 3 (saukett), haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate) conjugated to tetanus protein - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - vaccines, bacterial and viral vaccines, combined - hexacima (dtap-ipv-hb-hib) je indicirano za osnovno in obnovitveno cepljenje dojenčkov in malčkov iz šestih tednih starosti proti davici, tetanus, oslovski kašelj, hepatitis b, otroški ohromelosti in invazivnih bolezni, ki povzroča haemophilus influenzae tipa b (hib). uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Evropska unija - slovenščina - 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 - cepiva - hexyon (dtap-ipv-hb-hib) je indicirano za osnovno in obnovitveno cepljenje dojenčkov in malčkov iz šestih tednih starosti proti davici, tetanus, oslovski kašelj, hepatitis b, otroški ohromelosti in invazivnih bolezni, ki povzroča haemophilus influenzae tipa b (hib). uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Evropska unija - slovenščina - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin), hepatitis b surface antigen, poliovirus (inactivated) (type-1 (mahoney strain), type-2 (mef-1 strain), type-3 (saukett strain)), haemophilus influenzae type b polysaccharide - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - cepiva - infanrix hexa je indicirano za osnovno in obnovitveno cepljenje dojenčkov proti davici, tetanus, oslovski kašelj, hepatitis b, otroški ohromelosti in bolezen, ki povzroča haemophilus influenzae tipa b.

Evropska unija - slovenščina - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - inaktiviran virus splitskega virusa, ki vsebuje antigen, ki ustreza sevu a / california / 07/2009 (h1n1), ki se uporablja nymc x-179a - influenza, human; immunization; disease outbreaks - cepiva proti gripi - preprečevanje gripe, ki jo povzroča virus a (h1n1) v 2009. pandemrix se lahko uporablja le, če priporočeni letni sezonsko gripo trivalentno / štirivalenten cepiv ni na voljo, in če je potrebno cepljenje proti (h1n1) v (glej točki 4. 4 in 4. pandemrix je treba uporabljati v skladu z uradnimi smernice.

Evropska unija - slovenščina - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - hepatitis b, rekombinantni površinski antigen - hepatitis b; immunization - cepiva - 5 micrograms hbvaxpro is indicated for active immunisation against hepatitis-b-virus infection caused by all known subtypes in individuals from birth through 15 years of age considered at risk of exposure to hepatitis-b virus. posebno ogroženih kategorij, da se immunised določi na podlagi uradnih priporočil. pričakovati je, da se hepatitis d bo prav tako mogoče preprečiti z imunizacijo z hbvaxpro, kot je hepatitis d (zaradi delta agent) ne pride v odsotnosti hepatitis-b, okužbe. 10 micrograms hbvaxpro is indicated for active immunisation against hepatitis-b-virus infection caused by all known subtypes in individuals 16 years of age or more considered at risk of exposure to hepatitis-b virus. posebno ogroženih kategorij, da se immunised določi na podlagi uradnih priporočil. pričakovati je, da se hepatitis d bo prav tako mogoče preprečiti z imunizacijo z hbvaxpro, kot je hepatitis d (zaradi delta agent) ne pride v odsotnosti hepatitis-b, okužbe. 40 micrograms hbvaxpro is indicated for the active immunisation against hepatitis-b-virus infection caused by all known subtypes in predialysis and dialysis adult patients. pričakovati je, da se hepatitis d bo prav tako mogoče preprečiti z imunizacijo z hbvaxpro, kot je hepatitis d (zaradi delta agent) ne pride v odsotnosti hepatitis b okužbe.

Evropska unija - slovenščina - EMA (European Medicines Agency)

intervet international b.v. - prašičji cirkovirus tipa 2 orf2 podenotnega antigena - immunologicals for suidae, inactivated viral vaccines - prašiči - for the active immunisation of pigs to reduce viraemia, virus load in lungs and lymphoid tissues and virus shedding caused by pcv2 infection.  to reduce loss of daily weight gain and mortality associated with pcv2 infection.

Evropska unija - slovenščina - EMA (European Medicines Agency)

intervet international bv - subigenski antigen klasične prašičje kuge (csfv) -e2 - imunologija za suidae - prašiči - aktivna imunizacija prašičev od starosti 5 tednov naprej, da se prepreči smrtnost in zmanjša klinični znaki klasične prašičje kuge, pa tudi zmanjša okužba in izločanje virusa terapije s csf. začetek zaščite je 2 tedna. trajanje zaščite je 6 mesecev.

Evropska unija - slovenščina - EMA (European Medicines Agency)

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - limfom, mantle cell - antineoplastična sredstva - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).