Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

pfizer europe ma eeig  - пегфилграстин - Неутропения - Иммуностимуляторы, - Намаляване на продължителността на неутропения и честотата на фебрилна неутропения при възрастни пациенти, лекувани с цитотоксична химиотерапия за злокачествено заболяване (с изключение на хронична миелоидна левкемия и миелодиспластични синдроми).

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

roche registration gmbh - pertuzumab, trastuzumab - Неоплазми на гърдата - Антинеопластични средства - early breast cancer (ebc)phesgo is indicated for use in combination with chemotherapy in:the neoadjuvant treatment of adult patients with her2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrencethe adjuvant treatment of adult patients with her2-positive early breast cancer at high risk of recurrencemetastatic breast cancer (mbc)phesgo is indicated for use in combination with docetaxel in adult patients with her2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-her2 therapy or chemotherapy for their metastatic disease.

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - trastuzumab deruxtecan - Неоплазми на гърдата - Антинеопластични средства - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

samsung bioepis nl b.v. - ранимизумаб - wet macular degeneration; macular edema; diabetic retinopathy; myopia, degenerative - Офталмологични - byooviz is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

sanofi pasteur - sars-cov-2 prefusion spike delta tm protein, recombinant (b.1.351 strain) - covid-19 virus infection - Ваксини - vidprevtyn beta is indicated as a booster for active immunisation to prevent covid-19 in adults who have previously received an mrna or adenoviral vector covid-19 vaccine (see sections 4. 2 и 5. 1 in product information document). Използването на тази ваксина трябва да бъде приложена в съответствие с официалните препоръки.

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - mirikizumab - Колит, язвена - Имуносупресори - omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

novartis europharm limited - ранимизумаб - wet macular degeneration; macular edema; diabetes complications; myopia, degenerative; choroidal neovascularization - Офталмологични - Луцентис е показан при възрастни за лечение на неоваскулярной (влажна) на възрастовата макулна дегенерация (amd)лечение на нарушения на зрението, вследствие на хориоидальной неоваскуляризации (ХНВ)лечение на нарушения на зрението, вследствие на диабетического оток на макулата (ДМО)лечение на нарушения на зрението, вследствие на оток на макулата вторично запушване ретинальных вени (клон или централна РДЛ РДЛ).

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

pfizer europe ma eeig - мороктоког алфа - Хемофилия А - Антихеморагични - Лечение и профилактика на кървене при пациенти с хемофилия А (вродена дефицит на фактор vІІІ). refacto af не са подходящи за употреба при възрастни и деца от всички възрасти, включително новородени. refacto af не съдържа фон-Виллебранда фактор, и, следователно, не посочи при болестта на фон Виллебранда .

Եվրոպական Միություն - բուլղարերեն - EMA (European Medicines Agency)

biosimilar collaborations ireland limited - пегфилграстин - Неутропения - Иммуностимуляторы, - Намаляване на продължителността на неутропения и честотата на фебрилна неутропения при възрастни пациенти, лекувани с цитотоксична химиотерапия за злокачествено заболяване (с изключение на хронична миелоидна левкемия и миелодиспластични синдроми).

Եվրոպական Միություն - բուլղարերեն - 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.