PROPOFOL HOSPIRA süste-/infusiooniemulsioon Эстония - эстонский - Ravimiamet

propofol hospira süste-/infusiooniemulsioon

hospira uk limited - propofool - süste-/infusiooniemulsioon - 10mg 1ml 100ml 10tk; 10mg 1ml 50ml 1tk; 10mg 1ml 50ml 5tk; 10mg 1ml 100ml 20tk

Oxlumo Европейский союз - эстонский - EMA (European Medicines Agency)

oxlumo

alnylam netherlands b.v. - lumasiran sodium - hyperoxaluria, primary - muud alimentary seedetrakti ja ainevahetust tooted, - treatment of primary hyperoxaluria type 1 (ph1) in all age groups.

Vocabria Европейский союз - эстонский - EMA (European Medicines Agency)

vocabria

viiv healthcare b.v. - cabotegavir sodium, cabotegravir - hiv-nakkused - viirusevastased ravimid süsteemseks kasutamiseks - vocabria tablets are indicated in combination with rilpivirine tablets for the short-term treatment of human immunodeficiency virus type 1 (hiv-1) infection in adults who are virologically suppressed (hiv-1 rna.

Sugammadex Mylan Европейский союз - эстонский - EMA (European Medicines Agency)

sugammadex mylan

mylan ireland limited - sugammadex sodium - neuromuskulaarne blokaad - kõik muud ravitoimingud - reversal of neuromuscular blockade induced by   rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Fresenius Kabi Европейский союз - эстонский - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - neuromuskulaarne blokaad - kõik muud ravitoimingud - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Amvuttra Европейский союз - эстонский - EMA (European Medicines Agency)

amvuttra

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - muud närvisüsteemi ravimid - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Sugammadex Amomed Европейский союз - эстонский - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromuskulaarne blokaad - kõik muud ravitoimingud - rookurooniumi või vekurooniumi poolt indutseeritud neuromuskulaarse blokaadi pöördumine. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Piramal Европейский союз - эстонский - EMA (European Medicines Agency)

sugammadex piramal

piramal critical care b.v. - sugammadex sodium - neuromuskulaarne blokaad - sugammadeks - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.

Sugammadex Adroiq Европейский союз - эстонский - EMA (European Medicines Agency)

sugammadex adroiq

extrovis eu ltd. - sugammadex sodium - neuromuskulaarne blokaad - kõik muud ravitoimingud - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

MOLAXOLE suukaudse lahuse pulber Эстония - эстонский - Ravimiamet

molaxole suukaudse lahuse pulber

meda pharma sia - makrogool+naatriumkloriid+naatriumvesinikkarbonaat+kaaliumkloriid - suukaudse lahuse pulber - 13,125mg+350,7mg+178,5mg+46,6mg 30tk; 13,125mg+350,7mg+178,5mg+46,6mg 20tk; 13,125mg+350,7mg+178,5mg+46,6mg 2tk; 13,125mg+350,7mg+178,5mg+46,6mg 8tk; 13,125mg+350,7mg+178,5mg+46,6mg 6tk; 13,125mg+350,7mg+178,5mg+46,6mg 60tk; 13,125mg+350,7mg+178,5mg+46,6mg 100tk; 13,125mg+350,7mg+178,5mg+46,6mg 10tk