Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

ceva santé animale - инактивирана ваксина срещу coxiella burnetii, щам nine mile - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains) - Имуномодулатори за котки,на - Котки - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs. onsets of immunity isone week after primary vaccination course. the duration of immunity is one year after primary vaccination course and three years after the last re-vaccination.

Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline panleucopenia virus (pli iv) - Имуномодулатори за котки,на - Котки - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs. onset of immunity is one week after primary vaccination course the duration of immunity is one year after the primary vaccination course and three years after the last re-vaccination.

Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

merck sharp and dohme b.v - позаконазол - candidiasis; mycoses; coccidioidomycosis; aspergillosis - Антимикотици за системна употреба - noxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 и 5. 1):- invasive aspergillosisnoxafil gastro-resistant tablets are indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections  4. 2 и 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Огнеупорность се определя като прогресията на инфекция или липса на подобрение след минимум 7 дни преди терапевтични дози ефективна терапия противогрибковой. noxafil gastro-resistant tablets are also indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2 years of age weighing more than 40 kg and adults (see sections 4. 2 и 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adults (see sections 4. 2 и 5. 1):- invasive aspergillosisnoxafil concentrate for solution for infusion is indicated for use in the treatment of the following fungal infections in adult and paediatric patients from 2 years of age (see sections 4. 2 и 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Огнеупорность се определя като прогресията на инфекция или липса на подобрение след минимум 7 дни преди терапевтични дози ефективна терапия противогрибковой. noxafil concentrate for solution for infusion is also indicated for prophylaxis of invasive fungal infections in the following adult and paediatric patients from 2 years of age (see sections 4. 2 и 5. 1):- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease (gvhd) and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil gastro resistant powder and solvent for oral suspension is indicated for use in the treatment of the following fungal infections in paediatric patients from 2 years of age (see sections 4. 2 и 5. 1):- invasive aspergillosis in patients with disease that is refractory to amphotericin b or itraconazole or in patients who are intolerant of these medicinal products;- fusariosis in patients with disease that is refractory to amphotericin b or in patients who are intolerant of amphotericin b;- chromoblastomycosis and mycetoma in patients with disease that is refractory to itraconazole or in patients who are intolerant of itraconazole;- coccidioidomycosis in patients with disease that is refractory to amphotericin b, itraconazole or fluconazole or in patients who are intolerant of these medicinal products. Огнеупорность се определя като прогресията на инфекция или липса на подобрение след минимум 7 дни преди терапевтични дози ефективна терапия противогрибковой. noxafil gastro-resistant powder and solvent for oral suspension is indicated for prophylaxis of invasive fungal infections in the following paediatric patients from 2  years of age:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high  risk of developing invasive fungal infections;- haematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high  risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis. please refer to the summary of product characteristics of noxafil oral suspension for use in oropharyngeal candidiasis.  noxafil oral suspension is indicated for use in the treatment of the following fungal infections in adults (see section 5. 1):- инвазивна аспергилоза при пациенти с болестта, продължителна към амфотерицину В или итраконазолу, или при пациенти с непоносимост към тези лекарства;- fusarium при пациенти с болестта, продължителна към амфотерицину В или при пациенти, които имат непоносимост амфотерицин В;- chromoblastomycosis и мицетома при пациенти с болестта, рефрактерного до итраконазолу или при пациенти с непоносимост итраконазола;- Кокцидиоидомикоз при пациенти с болестта, продължителна към амфотерицину, итраконазолу или флуконазолу, или при пациенти с непоносимост към тези лекарства;- Орофарингеальный кандидоза: като първа линия терапия при пациенти, страдащи от тежки заболявания или са имунно-компрометирани, в които отговор на актуални терапия, както се очаква, ще бъде лошо. Огнеупорность се определя като прогресията на инфекция или липса на подобрение след минимум 7 дни преди терапевтични дози ефективна терапия противогрибковой. noxafil oral suspension is also indicated for prophylaxis of invasive fungal infections in the following patients:- patients receiving remission-induction chemotherapy for acute myelogenous leukaemia (aml) or myelodysplastic syndromes (mds) expected to result in prolonged neutropenia and who are at high risk of developing invasive fungal infections;- hematopoietic stem cell transplant (hsct) recipients who are undergoing high-dose immunosuppressive therapy for graft versus host disease and who are at high risk of developing invasive fungal infections. please refer to the summary of product characteristics of noxafil concentrate for solution for infusion and the gastro-resistant tablets for use in primary treatment of invasive aspergillosis.

Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

amgen europe b.v. - ромиплостим - Пурпура, Тромбоцитопения, Идиопатична - Антихеморагични - adults:nplate is indicated for the treatment of primary immune thrombocytopenia  (itp) in adult patients who are refractory to other treatments (e. кортикостероиди, имуноглобулини). paediatrics:nplate is indicated for the treatment of chronic primary immune thrombocytopenia (itp) in paediatric patients one year of age and older who are refractory to other treatments (e. кортикостероиди, имуноглобулини).

Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

novartis europharm limited - eltrombopag - Пурпура, Тромбоцитопения, Идиопатична - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 и 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 и 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.

Euroopa Liit - bulgaaria - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - Дабигатрана этексилат мезилат - arthroplasty, replacement; venous thromboembolism - Антитромботични агенти - Этексилат 75 mgprimary профилактика венозных тромбоемболични усложнения при възрастни пациенти, които са избираеми общи подмяна на тазобедрена става или безогледно ендопротезиране на колянна става. Этексилат 110 mgprimary профилактика венозных тромбоемболични усложнения при възрастни пациенти, които са избираеми общи подмяна на тазобедрена става или безогледно ендопротезиране на колянна става. Профилактика на инсулт и системна емболия при възрастни пациенти с неклапанной фибрилляцией мъждене (nvaf), с един или повече рискови фактори, като например инсулт или транзиторная исхемична атака (ТИА); възраст ≥ 75 години; сърдечна недостатъчност (nyha клас ≥ втори); захарен диабет; хипертония. Лечение на дълбока венозна тромбоза (dvt) и тромбоэмболии белодробната артерия (ТЭЛА) и за превенция на рецидив на дълбока венозна тромбоза и ТЭЛА при възрастни. Этексилат 150 mgprevention инсулт и системна емболия при възрастни пациенти с неклапанной фибрилляцией мъждене (nvaf), с един или повече рискови фактори, като например инсулт или транзиторная исхемична атака (ТИА); възраст ≥ 75 години; сърдечна недостатъчност (nyha клас ≥ втори); захарен диабет; хипертония. Лечение на дълбока венозна тромбоза (dvt) и тромбоэмболии белодробната артерия (ТЭЛА) и за превенция на рецидив на дълбока венозна тромбоза и ТЭЛА при възрастни.

Bulgaaria - bulgaaria - БАБХ (Българска агенция по безопасност на храните)

Примавет – София ООД - Олеум Меnthае piperitae, thymolum - лента за пчелен кошер - 2,0 g/лента; 5,0 g/лента - пчели

Bulgaaria - bulgaaria - БАБХ (Българска агенция по безопасност на храните)

Примавет – София ООД - Резорцин, салицилова киселина, sulfathiazole - разтвор за кожа - 1, 6 g/100 ml; 1, 6 g/100 ml, 2, 5 g/100 ml - коне, котки, кучета

Bulgaaria - bulgaaria - БАБХ (Българска агенция по безопасност на храните)

Примавет – София ООД - Мегестрола ацетат - таблетка - 10 mg/таблетка - котки, кучета