Tabrecta Euroopa Liit - eesti - EMA (European Medicines Agency)

tabrecta

novartis europharm limited  - capmatinib dihydrochloride monohydrate - kartsinoom, mitteväikerakk-kopsu - antineoplastilised ained - tabrecta as monotherapy is indicated for the treatment of adult patients with advanced non small cell lung cancer (nsclc) harbouring alterations leading to mesenchymal epithelial transition factor gene exon 14 (metex14) skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum based chemotherapy.

Tyenne Euroopa Liit - eesti - 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.

PecFent Euroopa Liit - eesti - EMA (European Medicines Agency)

pecfent

kyowa kirin holdings b.v. - fentanüül - pain; cancer - valuvaigistid - pecfent on näidustatud läbilöögivalu juhtimiseks täiskasvanutel, kes saavad kroonilise vähivastase valu alustamist hooldus opioidideks. läbimurrevalu on vahelduv valu ägenemine, mis esineb muidu kontrollitud püsiva valu taustal. saavate patsientide hooldus opioidide ravi on need, kes on võttes vähemalt 60 mg suukaudset morfiini päevas, vähemalt 25 mikrogrammi transdermaalset fentanüüli tunnis, vähemalt 30 mg oksükodoon päevas, vähemalt 8 mg suukaudse hüdromorfoon iga päev või equi-valuvaigistav annus teise opioidi ühe nädala jooksul või kauem,.

VANCOMYCIN PHARMASWISS infusioonilahuse pulber Eesti - eesti - Ravimiamet

vancomycin pharmaswiss infusioonilahuse pulber

pharmaswiss ceska republika s.r.o. - vankomütsiin - infusioonilahuse pulber - 1000mg 1tk; 1000mg 10tk

Embotape suukaudne pasta Eesti - eesti - Ravimiamet

embotape suukaudne pasta

bimeda animal health limited - püranteel - suukaudne pasta - 400mg 1g 28.5g 1tk

VANCOMYCIN PHARMASWISS infusioonilahuse pulber Eesti - eesti - Ravimiamet

vancomycin pharmaswiss infusioonilahuse pulber

pharmaswiss ceska republika s.r.o. - vankomütsiin - infusioonilahuse pulber - 500mg 10tk

Aservo EquiHaler Euroopa Liit - eesti - EMA (European Medicines Agency)

aservo equihaler

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)).