에스토니아 - 에스토니아어 - Ravimiamet

actavis group ptc ehf. - vankomütsiin - infusioonilahuse kontsentraadi pulber - 500mg 500mg 1tk

에스토니아 - 에스토니아어 - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 1mg 50tk; 1mg 100tk; 1mg 30tk; 1mg 60tk

에스토니아 - 에스토니아어 - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 5mg 100tk; 5mg 50tk; 5mg 30tk; 5mg 60tk

에스토니아 - 에스토니아어 - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 3mg 30tk; 3mg 50tk; 3mg 60tk

에스토니아 - 에스토니아어 - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 0,5mg 50tk; 0,5mg 30tk; 0,5mg 60tk

에스토니아 - 에스토니아어 - Ravimiamet

sandoz pharmaceuticals d.d. - takroliimus - toimeainet prolongeeritult vabastav kõvakapsel - 2mg 100tk; 2mg 60tk; 2mg 50tk

유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - ciclesonide - hingamiselundite muud ravimid hingamisteede obstruktiivsete haiguste, inhalants - hobused - eest leevendamine kliinilised tunnused on raske hobuste astma (varem tuntud korduvad hingamisteede obstruktsioon – (rao), suvel karjamaal seotud korduvate hingamisteede obstruktsioon – (spa-rao)).

유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

curium pet france - piflufolastat (18f) - eesnäärmevähk - diagnostilised radiofarmatseutilised ühendid - see ravim on mõeldud ainult diagnostiliseks kasutamiseks. pylclari is indicated for the detection of prostate-specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high-risk pca prior to initial curative therapy,to localize recurrence of pca in patients with a suspected recurrence based on increasing serum prostate-specific antigen (psa) levels after primary treatment with curative intent. pylclari is indicated for use with positron emission tomography (pet).

유럽 연합 - 에스토니아어 - EMA (European Medicines Agency)

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.