paracetamol arena suukaudne lahus
meduman s.a. - paratsetamool - suukaudne lahus - 24mg 1ml 100ml 1tk
meloxivet
eli lilly and company limited - meloksikaam - lihas-skeleti süsteem - koerad - põletiku ja valu leevendamine nii ägedate kui ka krooniliste lihas-skeleti kahjustuste korral.
magnegita süstelahus
agfa healthcare imaging agents gmbh - gadopenteethape - süstelahus - 469mg 1ml 30ml 1tk; 469mg 1ml 5ml 10tk; 469mg 1ml 30ml 10tk; 469mg 1ml 10ml 10tk; 469mg 1ml 5ml 1tk; 469mg 1ml 10ml 1tk; 469mg 1ml 100ml 1tk; 469mg 1ml 100ml 10tk; 469mg 1ml 15ml 1tk; 469mg 1ml 20ml 1tk; 469mg 1ml 15ml 10tk
hypothiazid tablett
sanofi winthrop industrie - hüdroklorotiasiid - tablett - 25mg 20tk
spironolacton- ratiopharm 50mg tablett
ratiopharm gmbh - spironolaktoon - tablett - 50mg 50tk; 50mg 20tk
circadin
rad neurim pharmaceuticals eec sarl - melatoniin - unehäirete ja hoolduse häired - psühhoeptikumid - circadin on näidustatud, kui monoteraapia primaarse unetuse lühiajaliseks raviks, mida iseloomustab halva kvaliteediga uni vähemalt 55 saavatel või üle.
incivo
janssen-cilag international n.v. - telapreviir - c-hepatiit, krooniline - viirusevastased ravimid süsteemseks kasutamiseks - incivo, koos peginterferon alfa ja ribavirin, on näidustatud ravi genotüüp-1 krooniline hepatiit c täiskasvanud patsientidel, kellel on kompenseeritud maksahaigus (sh tsirroos):kes on ravi naiivne, kes on varem ravitud interferoon alfa (pegylated või mitte-pegylated), üksi või koos ribavirin, sealhulgas relapsers, osaline ravile ja null ravile.
olysio
janssen-cilag international nv - simeprevir - c-hepatiit, krooniline - viirusevastased ravimid süsteemseks kasutamiseks - olysio on näidustatud kombinatsioonis teiste kroonilise hepatiit c (chc) ravimitega täiskasvanud patsientidel. c-hepatiidi viiruse (hcv) genotüüp spetsiifiline aktiivsus.
slenyto
rad neurim pharmaceuticals eec sarl - melatoniin - sleep initiation and maintenance disorders; autistic disorder - psühhoeptikumid - slenyto on näidustatud ravi unetust lastel ja noorukitel vanuses 2-18 autismi spektri häire (asd) ja / või smith-magenis sündroomi, kus une hügieeni meetmed on ebapiisavad,.
ultomiris
alexion europe sas - ravulizumab - hemoglobinuuria, paroksüsmaalne - selektiivsed immunosupressandid - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.