kodein "dak" 3 mg/ml oral opl?sning
orifarm healthcare a/s - codeinphosphathemihydrat - oral opløsning - 3 mg/ml
kodein stærk "dak" 8 mg/ml oral opløsning
orifarm healthcare a/s - codein - oral opløsning - 8 mg/ml
moniyot-131 capsule t 37-7400 mb kapsler, hårde
monrol europe s.r.l. - natriumiodid (131-i) - kapsler, hårde - 37-7400 mb
accurate delta vanddispergerbart granulat
fmc agricultural solutions a/s (tidligere: cheminova a/s) - diflufenican, metsulfuron-methyl, metsulfuron - vanddispergerbart granulat - 600 g/kg diflufenican ; 60 g/kg metsulfuron-methyl ; (~ 57,8 g/kg metsulfuron
cha 3554 flydende middel
cheminova a/s - dimethoat, gamma-cyhalothrin - flydende middel - 400 g/l dimethoat; 4 g/l gamma-cyhalothrin
cha 3556 flydende middel
cheminova a/s - dimethoat, gamma-cyhalothrin - flydende middel - 400 g/l dimethoat; 6,4 g/l gamma-cyhalothrin
cerall flydende bejdse
bioagri ab / lantmännen bioagri - pseudomonas - flydende bejdse - 10000000000 cfu/ml pseudomonas chlororaphis stamme ma342
alunbrig
takeda pharma a/s - brigatinib - carcinom, ikke-småcellet lunge - antineoplastiske midler - alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase alkpositive advanced nsclc previously treated with crizotinib.
ultomiris
alexion europe sas - ravulizumab - hemoglobinuri, paroxysmal - selektive immunosuppressiva - 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.
salifort pulver
isa nanotech bv - kalium, fosfor - pulver - 381,8 g/kg kalium ; 104,9 g/kg fosfor