Europska Unija - bugarski - EMA (European Medicines Agency)

lipomed gmbh - Деферипрон - iron overload; beta-thalassemia - Всички други терапевтични продукти - Деферипрон lipomed монотерапии, предназначени за лечение на претоварване с желязо при пациенти с талассемией майор, когато текущата хелаторная терапия противопоказан или неадекватна. Деферипрон lipomed в комбинация с друга хелатор е показан при пациенти с талассемией майор, когато монотерапия с всеки хелатор на желязото неефективни, или за профилактика или лечение на животозастрашаващи последици от претоварване с желязо оправдава бързо или интензивно корекция.

Europska Unija - bugarski - EMA (European Medicines Agency)

novartis europharm limited  - voretigene neparvovec - leber congenital amaurosis; retinitis pigmentosa - other ophthalmologicals - luxturna е показан за лечение и педиатрични възрастни пациенти със загуба на зрението поради наследство дистрофия на ретината, причинени от потвърди rpe65 биаллельных мутации, които са достатъчно жизнеспособни клетки на ретината.

Europska Unija - bugarski - EMA (European Medicines Agency)

janssen-cilag international n.v.   - палиперидон палмитат - шизофрения - психолептици - byannli (previously paliperidone janssen-cilag international) a 6 monthly injection, is indicated for the maintenance treatment of schizophrenia in adult patients who are clinically stable on 1 monthly or 3 monthly paliperidone palmitate injectable products (see section 5.

Europska Unija - bugarski - EMA (European Medicines Agency)

pacira ireland limited - bupivacaine - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

Europska Unija - bugarski - EMA (European Medicines Agency)

nova laboratories ireland limited - azathioprine - Отхвърляне на присадката - Имуносупресори - jayempi is indicated in combination with other immunosuppressive agents for the prophylaxis of transplant rejection in patients receiving allogenic kidney, liver, heart, lung or pancreas transplants. azathioprine is indicated in immunosuppressive regimens as an adjunct to immunosuppressive agents that form the mainstay of treatment (basis immunosuppression). jayempi is used as an immunosuppressant antimetabolite either alone or, more commonly, in combination with other agents (usually corticosteroids) and/ or procedures which influence the immune response. jayempi is indicated in patients who are intolerant to glucocorticosteroids or if the therapeutic response is inadequate despite treatment with high doses of glucocorticosteroids, in the following diseases:severe active rheumatoid arthritis (chronic polyarthritis) that cannot be kept under control by less toxic agents (disease-modifying anti-rheumatic -medicinal products – dmards)auto-immune hepatitis systemic lupus erythematosusdermatomyositispolyarteritis nodosapemphigus vulgaris and bullous pemphigoidbehçet’s diseaserefractory auto-immune haemolytic anaemia, caused by warm igg antibodieschronic refractory idiopathic thrombocytopenic purpurajayempi is used for the treatment of moderately severe to severe forms of chronic inflammatory bowel disease (ibd) (crohn’s disease or ulcerative colitis) in patients in whom glucocorticosteroid therapy is necessary, but where glucocorticosteroids are not tolerated, or in whom the disease is untreatable with other common means of first choice. it is also indicated in adult patients in relapsing multiple sclerosis, if an immunomodulatory therapy is indicated but beta interferon therapy is not possible, or a stable course has been achieved with previous treatment with azathioprine. 3jayempi is indicated for the treatment of generalised myasthenia gravis. depending on the severity of the disease, jayempi should be given in combination with glucocorticosteroids because of slow onset of action at the beginning of treatment and the glucocorticosteroid dose should be gradually reduced after several months of treatment.

Europska Unija - bugarski - EMA (European Medicines Agency)

novartis europharm limited - asciminib hydrochloride - Левкемия, миелогенна, хронична, bcr-abl положителна - Антинеопластични средства - scemblix is indicated for the treatment of adult patients with philadelphia chromosome positive chronic myeloid leukaemia in chronic phase (ph+ cml cp) previously treated with two or more tyrosine kinase inhibitors (see section 5.

Europska Unija - bugarski - EMA (European Medicines Agency)

novartis europharm limited  - lutetium (177lu) vipivotide tetraxetan - Новообразувания На Простатата, Кастраци-Упорит - Терапевтични радиофармацевтици - pluvicto in combination with androgen deprivation therapy (adt) with or without androgen receptor (ar) pathway inhibition is indicated for the treatment of adult patients with progressive prostate-specific membrane antigen (psma)-positive metastatic castration-resistant prostate cancer (mcrpc) who have been treated with ar pathway inhibition and taxane based chemotherapy.

Europska Unija - bugarski - EMA (European Medicines Agency)

csl behring gmbh - лококтоког алфа - Хемофилия А - Антихеморагични - Лечение и профилактика на кървене при пациенти с хемофилия А (дефицит на вроден дефицит на фактор vІІІ). afstyla може да се използва за всички възрастови групи.

Europska Unija - bugarski - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - Други антинеопластични средства - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Europska Unija - bugarski - EMA (European Medicines Agency)

santen oy - циклоспорин - conjunctivitis; keratitis - Офталмологични - Лечението на тежки пролетта кератоконъюнктивит (ВКС) при деца на възраст от 4 години и тийнейджъри.