TENECTELEX süstelahuse pulber ja lahusti Estònia - estonià - Ravimiamet

tenectelex süstelahuse pulber ja lahusti

reliance life sciences pvt. ltd - tenekteplaas - süstelahuse pulber ja lahusti - 40mg 1tk

Daklinza Unió Europea - estonià - EMA (European Medicines Agency)

daklinza

bristol-myers squibb pharma eeig - daclatasvirdihüdrokloriid - c-hepatiit, krooniline - viirusevastased ravimid süsteemseks kasutamiseks - daklinza on näidustatud kombinatsioonis teiste kroonilise hepatiit c viiruse (hcv) nakkuse raviks mõeldud ravimitega täiskasvanutel (vt lõigud 4. 2, 4. 4 ja 5. sest hcv genotüüp konkreetne tegevus, vt punktid 4. 4 ja 5.

Sunitinib Accord Unió Europea - estonià - EMA (European Medicines Agency)

sunitinib accord

accord healthcare s.l.u. - sunitiniib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastilised ained - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

ULIPRISTAL ACETATE SANDOZ õhukese polümeerikattega tablett Estònia - estonià - Ravimiamet

ulipristal acetate sandoz õhukese polümeerikattega tablett

sandoz pharmaceuticals d.d. - ulipristaal - õhukese polümeerikattega tablett - 30mg 1tk

Nitisinone MDK (previously Nitisinone MendeliKABS) Unió Europea - estonià - EMA (European Medicines Agency)

nitisinone mdk (previously nitisinone mendelikabs)

mendelikabs europe ltd - nitisinoon - türosineemiad - muud alimentary seedetrakti ja ainevahetust tooted, - raviks täiskasvanutel ja lastel (on vanus vahemikus) kinnitatud diagnoosi pärilik tyrosinemia tüüpi 1 (ht 1) koos metioniinisisaldust türosiini ja fenüülalaniini.

Tyenne Unió Europea - estonià - EMA (European Medicines Agency)

tyenne

fresenius kabi deutschland gmbh - totsilizumab - arthritis, rheumatoid; cytokine release syndrome; arthritis, juvenile rheumatoid; covid-19 virus infection; giant cell arteritis - immunosupressandid - tyenne, in combination with methotrexate (mtx), is indicated for- the treatment of severe, active and progressive rheumatoid arthritis (ra) in adults not previously treated with mtx. - the treatment of moderate to severe active ra in adult patients who have either responded inadequately to, or who were intolerant to, previous therapy with one or more disease-modifying anti-rheumatic drugs (dmards) or tumour necrosis factor (tnf) antagonists. in these patients, tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tocilizumab has been shown to reduce the rate of progression of joint damage as measured by x-ray and to improve physical function when given in combination with methotrexate. tyenne is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who are receiving systemic corticosteroids and require supplemental oxygen or mechanical ventilation. tyenne is indicated for the treatment of active systemic juvenile idiopathic arthritis (sjia) in patients 1 year of age and older, who have responded inadequately to previous therapy with nsaids and systemic corticosteroids. tyenne can be given as monotherapy (in case of intolerance to mtx or where treatment with mtx is inappropriate) or in combination with mtx. tyenne in combination with methotrexate (mtx) is indicated for the treatment of juvenile idiopathic polyarthritis (pjia; rheumatoid factor positive or negative and extended oligoarthritis) in patients 2 years of age and older, who have responded inadequately to previous therapy with mtx. tyenne can be given as monotherapy in case of intolerance to mtx or where continued treatment with mtx is inappropriate. tyenne is indicated for the treatment of chimeric antigen receptor (car) t cell-induced severe or life-threatening cytokine release syndrome (crs) in adults and paediatric patients 2 years of age and older. tyenne is indicated for the treatment of giant cell arteritis (gca) in adult patients.

Stresnil süstelahus Estònia - estonià - Ravimiamet

stresnil süstelahus

elanco france s.a.s. - asaperoon - süstelahus - 40mg 1ml 100ml 1tk

Zolvix suukaudne lahus Estònia - estonià - Ravimiamet

zolvix suukaudne lahus

elanco france s.a.s. - monepanteel - suukaudne lahus - 25mg 1ml 1000ml 1tk; 25mg 1ml 500ml 1tk

Atopica pehmekapsel Estònia - estonià - Ravimiamet

atopica pehmekapsel

elanco france s.a.s. - tsüklosporiin - pehmekapsel - 50mg 30tk

Atopica pehmekapsel Estònia - estonià - Ravimiamet

atopica pehmekapsel

elanco france s.a.s. - tsüklosporiin - pehmekapsel - 100mg 30tk