Viro - viro - Ravimiamet

virbac - koerte katku elusviirusvaktsiin+koerte elus parvoviirusvaktsiin+koerte nakkava hepatiidi elusviirusvaktsiin+koerte paragripi elusviirusvaktsiin - süstesuspensiooni lüofilisaat ja lahusti - 1annus 1annus 50tk; 1annus 1annus 10tk

Viro - viro - Ravimiamet

merial - koerte katku elusviirusvaktsiin+koerte elus parvoviirusvaktsiin+koerte nakkava hepatiidi elusviirusvaktsiin+koerte paragripi elusviirusvaktsiin - süstesuspensiooni pulber ja lahusti - 10000ccid50+0+0+0 1annus 1annus 10tk; 10000ccid50+0+0+0 1annus 1annus 1tk

Viro - viro - Ravimiamet

boehringer ingelheim animal health france - koerte katku elusviirusvaktsiin+koerte nakkava hepatiidi elusviirusvaktsiin+koerte elus parvoviirusvaktsiin+leptospira inaktiveeritud vaktsiin - süstesuspensiooni lüofilisaat ja suspensioon - 1annus 1ml 50annus; 1annus 1ml 25annus

Viro - viro - Ravimiamet

boehringer ingelheim animal health france - koerte katku elusviirusvaktsiin+koerte nakkava hepatiidi elusviirusvaktsiin+koerte elus parvoviirusvaktsiin+koerte paragripi elusviirusvaktsiin+leptospira inaktiveeritud vaktsiin+marutaudi inaktiveeritud viirusvaktsiin - süstesuspensiooni lüofilisaat ja suspensioon - 1annus 1annus 50tk; 1annus 1annus 1tk

Viro - viro - Ravimiamet

virbac - koerte katku elusviirusvaktsiin+koerte nakkava hepatiidi elusviirusvaktsiin+koerte paragripi elusviirusvaktsiin+koerte elus parvoviirusvaktsiin+leptospira inaktiveeritud vaktsiin - süstesuspensiooni pulber ja suspensioon - 1annus 1annus 10tk

Euroopan unioni - viro - EMA (European Medicines Agency)

pfizer europe ma eeig - glasdegib maleate - leukeemia, müeloidne, äge - antineoplastilised ained - daurismo is indicated, in combination with low-dose cytarabine, for the treatment of newly diagnosed de novo or secondary acute myeloid leukaemia (aml) in adult patients who are not candidates for standard induction chemotherapy.

Euroopan unioni - viro - EMA (European Medicines Agency)

eurogenerics holdings b.v. - teriparatiid - osteoporoos - kaltsiumi homöostaas - qutavina is indicated in adults. osteoporoosi ravi postmenopausis naistel ja meestel, kellel on suurem luumurdude risk. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. ravi osteoporoosi seostatakse pidevat süsteemset glükokortikoidi ravi naiste ja meeste suurenenud risk luumurdude.

Euroopan unioni - viro - EMA (European Medicines Agency)

novartis europharm limited - ruxolitiniib (fosfaadina) - myeloproliferative disorders; polycythemia vera; graft vs host disease - antineoplastilised ained - myelofibrosis (mf)jakavi is indicated for the treatment of disease related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. polycythaemia vera (pv)jakavi on näidustatud ravi täiskasvanud patsientidel, kellel polycythaemia vera, kes on resistentsed või sallimatu hydroxyurea. graft versus host disease (gvhd)jakavi is indicated for the treatment of patients aged 12 years and older with acute graft versus host disease or chronic graft versus host disease who have inadequate response to corticosteroids or other systemic therapies (see section 5.

Euroopan unioni - viro - EMA (European Medicines Agency)

adienne s.r.l. s.u. - melphalan hydrochloride - multiple myeloma; hodgkin disease; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; leukemia, myeloid, acute; neuroblastoma; ovarian neoplasms; hematopoietic stem cell transplantation - antineoplastilised ained - high-dose of phelinun used alone or in combination with other cytotoxic medicinal products and/or total body irradiation is indicated in the treatment of:multiple myeloma,malignant lymphoma (hodgkin, non-hodgkin lymphoma),acute lymphoblastic and myeloblastic leukemia,childhood neuroblastoma,ovarian cancer,mammary adenocarcinoma. phelinun in combination with other cytotoxic medicinal products is indicated as reduced intensity conditioning (ric) treatment prior to allogeneic haematopoietic stem cell transplantation (allo-hsct) in malignant haematological diseases in adults. phelinun in combination with other cytotoxic medicinal products is indicated as conditioning regimen prior to allogeneic haematopoietic stem cell transplantation in haematological diseases in the paediatric population as:myeloablative conditioning (mac) treatment in case of malignant haematological diseasesric treatment in case of non-malignant haematological diseases.

Euroopan unioni - viro - EMA (European Medicines Agency)

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.