intuniv
takeda pharmaceuticals international ag ireland branch - guanfacín hýdróklóríð - attention deficit disorder með ofvirkni - antiadrenergic agents, centrally acting, antihypertensives, - intuniv is indicated for the treatment of attention deficit hyperactivity disorder (adhd) in children and adolescents 6 17 years old for whom stimulants are not suitable, not tolerated or have been shown to be ineffective. intuniv verður að vera notað sem hluti af alhliða kynlÍf meðferð áætlun, venjulega þar á meðal sálfræðilega, mennta og félagslega mælist.
ultomiris
alexion europe sas - ravulizumab - blóðrauði, ofsakláði - valdar ónæmisbælandi lyf - 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.
seroquel prolong forðatafla 50 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 50 mg
seroquel prolong forðatafla 300 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 300 mg
seroquel prolong forðatafla 200 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 200 mg
seroquel prolong forðatafla 150 mg
cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 150 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 50 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 50 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 200 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 200 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 300 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 300 mg
quetiapine alvogen (quetiapin ratiopharm) forðatafla 400 mg
alvogen ehf. - quetiapinum fúmarat - forðatafla - 400 mg