nutriflex special infuusioneste, liuos
b. braun melsungen ag - aspartic acid, glutamic acid, alanine, arginine, calcium chloride dihydrate, glucose monohydrate, aminoacetic acid, histidine, isoleucine, potassium dihydrogen phosphate , potassium hydroxide, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophane, valine, sodium acetate trihydrate, sodium hydroxide, magnesium acetate tetrahydrate - infuusioneste, liuos - yhdistelmävalmisteet
citrafleet jauhe oraaliliuosta varten, annospussi
casen recordati, s.l. - citric acid anhydrous, magnesium oxide, light, sodium picosulfate - jauhe oraaliliuosta varten, annospussi - natriumpikosulfaatti
kanuma
alexion europe sas - sebelipase alfa - lipidimetabolia, synnynnäiset virheet - muut ruuansulatuselimistön sairauksien ja aineenvaihduntasairauksien lääkkeet, - kanuma on tarkoitettu pitkäaikaiselle entsyymikorvaushoidolle (ert) kaiken ikäisille potilaille, joilla on lysosomaalihappo-lipaasi (lal) -häiriö.
soliris
alexion europe sas - ekulitsumabi - hemoglobinuria, paroxysmal - immunosuppressantit - soliris on tarkoitettu aikuisten ja lasten hoitoon:kohtauksittainen yöllinen haemoglobinuria (pnh). todisteita kliininen hyöty on osoitettu potilailla, joilla on hemolyysi kanssa kliinisiä oireita(s) osoittaa korkea taudin aktiivisuus, riippumatta siitä, verensiirtoon historia (ks. kohta 5. epätyypillinen hemolyyttis-ureeminen oireyhtymä (ilmankäsittely-yksiköissä). soliris on tarkoitettu aikuisten hoitoon:tulenkestävät yleistynyt myastenia gravis (gmg) potilailla, jotka ovat anti-asetyylikoliini-reseptorin (achr) vasta-aineen positiivinen (ks. kohta 5. neuromyelitis optica kirjon (nmosd) potilailla, jotka ovat anti-aquaporin-4 (aqp4) vasta-aine positiivinen aaltomaisesti taudinkulku.
ultomiris
alexion europe sas - ravulizumab - hemoglobinuria, paroxysmal - selektiiviset immunosuppressantit - 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.
strensiq
alexion europe sas - asfotase alfa - hypofosfatasiafenotyypin - muut ruuansulatuselimistön sairauksien ja aineenvaihduntasairauksien lääkkeet, - strensiq on tarkoitettu pitkäaikaiselle entsyymikorvaushoidolle potilaille, joilla on lapsi-alkamainen hypophosphatasia, taudin luun oireiden hoitamiseksi.
rennie lakritsi imeskelytabletti
bayer oy - calcium carbonate, magnesium carbonate, heavy - imeskelytabletti - tavanomaiset aluminium/kalsium/magnesiumyhdisteet
parosept 1.2 mg/ml suuvesi
sunstar france - chlorhexidine digluconate - suuvesi - 1.2 mg/ml - klooriheksidiini
medipekt 0.8 mg/ml oraaliliuos
orion corporation - bromhexine hydrochloride - oraaliliuos - 0.8 mg/ml - bromiheksiini
kvilla oraaliliuos
aco hud nordic ab - extractum fluidum quillajae (lat.), ammonium chloride - oraaliliuos - yhdistelmävalmisteet