Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

billev pharma aps - lutetium (177lu) chloride - radionuklidų vaizdavimas - terapiniai radiofarmaciniai preparatai - lutetium (177lu) chloride billev is a radiopharmaceutical precursor, and it is not intended for direct use in patients. it is to be used only for the radiolabelling of carrier molecules that have been specifically developed and authorised for radiolabelling with lutetium (177lu) chloride.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

extrovis eu ltd. - lakozamidas - epilepsija - antiepileptics, - lacosamide adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. lacosamide adroiq is indicated as adjunctive therapyin the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

zoetis belgium sa - kiaulės circovirus rekombinantinis virusas (cpcv) 1-2, inaktyvuota - imunologiniai preparatai - kiaulės (paršeliai) - aktyvios imunizacijos kiaulių per amžius tris savaites nuo kiaulių circovirus tipas 2 (pcv2) siekiant sumažinti viruso kiekio kraujyje ir limfinių audinių ir organų pažeidimus limfinių audinių, susijusių su pcv2 infekcijos, taip pat sumažinti klinikinius požymius, įskaitant negautą dienos svorio prieaugis, mirtingumas, susijęs su po nujunkymo multisystemic išsekimo sindromas.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

laboratoire aguettant - sufentanilas citratas - skausmas - anestezijos - dzuveo is indicated for the management of acute moderate to severe pain in adult patients.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol, mometasone furoate - astma - vaistai nuo obstrukcinių kvėpavimo takų ligų, - bemrist breezhaler is indicated as a maintenance   treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

novartis europharm limited  - indacaterol acetate, mometasone furoate - astma - vaistai nuo obstrukcinių kvėpavimo takų ligų, - atectura breezhaler is indicated as a maintenance treatment of asthma in adults and adolescents 12 years of age and older not adequately controlled with inhaled corticosteroids and inhaled short acting beta2-agonists.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

argenx - efgartigimod alfa - myasthenia gravis - imunosupresantai - vyvgart is indicated as an add on to standard therapy for the treatment of adult patients with generalised myasthenia gravis (gmg) who are anti acetylcholine receptor (achr) antibody positive.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - respiraciniu sincitijaus infekcijos - vakcinos - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. Žr. 4 skyrius. 2 ir 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. naudoti šios vakcinos turėtų būti laikantis oficialių rekomendacijų.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

ucb pharma sa - certolizumab pegol - krono liga - imunosupresantai - cimzia, in combination with methotrexate (mtx), is indicated for the treatment of moderate to severe, active rheumatoid arthritis (ra) in adult patients when the response to disease-modifying antirheumatic drugs (dmard) including methotrexate, has been inadequate. cimzia gali būti suteikiamas kaip monotherapy atveju netolerancija, kad metotreksato ar kai tolesnis gydymas metotreksatu netinka. cimzia 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.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

teva pharma b.v. - budesonide, formoterol - astma - vaistai nuo obstrukcinių kvėpavimo takų ligų, - budesonide/formoterol teva pharma b. skiriamas tik suaugusiems, 18 metų ir vyresniems. asthmabudesonide/formoterol teva pharma b. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists.