Ervebo ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

ervebo

merck sharp & dohme b.v.  - rekombinantinis vezikulinio stomatito virusas (padermės indiana) su ištrinti voko glikoproteinas, pakeista zairas ebolavirus (padermės kikwit 1995) paviršiaus glikoproteino - hemoraginės karštligės, ebola - vakcinos - ervebo is indicated for active immunization of individuals 1 year of age or older to protect against ebola virus disease (evd) caused by zaire ebola virus. naudoti ervebo turėtų būti laikantis oficialių rekomendacijų.

Retsevmo ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

retsevmo

eli lilly nederland b.v. - selpercatinib - carcinoma, non-small-cell lung; thyroid neoplasms - antinavikiniai vaistai - retsevmo as monotherapy is indicated for the treatment of adults and adolescents 12 years and older with advanced ret-mutant medullary thyroid cancer (mtc)advanced ret fusion-positive non-small cell lung cancer (nsclc) not previously treated with a ret inhibitoradvanced ret fusion-positive thyroid cancer who require systematic therapy following prior treatment.

Skysona ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

skysona

bluebird bio (netherlands) b.v. - elivaldogene autotemcel - adrenoleukodystrophy - kiti nervų sistemos vaistai - 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.

Evkeeza ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

evkeeza

ultragenyx germany gmbh - evinacumab - hipercholesterolemija - lipidą keičiančios medžiagos - evkeeza is indicated as an adjunct to diet and other low-density lipoprotein-cholesterol (ldl-c) lowering therapies for the treatment of adult and adolescent patients aged 12 years and older with homozygous familial hypercholesterolaemia (hofh).

Human C1-esterase inhibitor CSL Behring লিত্ভা - লিথুয়েনীয় - SMCA (Valstybinė vaistų kontrolės tarnyba)

human c1-esterase inhibitor csl behring

csl behring gmbh - Žmogaus c1-esterazės inhibitorius - milteliai ir tirpiklis injekciniam ar infuziniam tirpalui - 500 tv - c1-inhibitor, plasma derived

Human C1-esterase inhibitor CSL Behring লিত্ভা - লিথুয়েনীয় - SMCA (Valstybinė vaistų kontrolės tarnyba)

human c1-esterase inhibitor csl behring

csl behring gmbh - Žmogaus c1-esterazės inhibitorius - milteliai ir tirpiklis injekciniam tirpalui - 1500 tv - c1-inhibitor, plasma derived

Sapropterin Dipharma ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

sapropterin dipharma

dipharma arzneimittel gmbh - sapropterin dihidrochloridas - phenylketonurias - kiti virškinimo trakto ir metabolizmo produktus, - sapropterin dipharma is indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with phenylketonuria (pku) who have been shown to be responsive to such treatment. sapropterin dipharma is also indicated for the treatment of hyperphenylalaninaemia (hpa) in adults and paediatric patients of all ages with tetrahydrobiopterin (bh4) deficiency who have been shown to be responsive to such treatment.

Cevenfacta ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

cevenfacta

laboratoire francais du fractionnement et des biotechnologies - eptacog beta (activated) - hemophilia a; hemophilia b - antihemoraginiai - cevenfacta is indicated in adults and adolescents (12 years of age and older) for the treatment of bleeding episodes and for the prevention of bleeding in those undergoing surgery or invasive procedures in the following patient groups:in patients with congenital haemophilia with high-responding inhibitors to coagulation factors viii or ix (i. ≥5 bethesda units (bu)); in patients with congenital haemophilia with low titre inhibitors (bu.

Ablavar (previously Vasovist) ইউরোপীয় ইউনিয়ন - লিথুয়েনীয় - EMA (European Medicines Agency)

ablavar (previously vasovist)

tmc pharma services ltd. - gadofosveset trisodium - magnetinio rezonanso angiografija - kontrasto terpė - Šis vaistas yra skirtas tik diagnostikai. ablavar yra nurodyta priešingai-sustiprinti magnetinio rezonanso angiografija (ce-mra) vizualizacijos, pilvo ar galūnių laivams tik suaugusiems, su įtariama arba žinoma kraujagyslių ligos.