pilexam 100 mg/ ml
pilum pharma a/s - traneksamsyre - injeksjonsvæske, oppløsning - 100 mg/ ml
salmeterol/fluticasone cipla 25 mikrog / 125 mikrog
cipla europe nv - salmeterolxinafoat / flutikasonpropionat - inhalasjonsaerosol, suspensjon - 25 mikrog / 125 mikrog
salmeterol/fluticasone cipla 25 mikrog / 250 mikrog
cipla europe nv - salmeterolxinafoat / flutikasonpropionat - inhalasjonsaerosol, suspensjon - 25 mikrog / 250 mikrog
ultomiris
alexion europe sas - ravulizumab - hemoglobinuri, paroksysmal - 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.
ondexxya
astrazeneca ab - andexanet alfa - narkotika-relaterte bivirkninger og uønskede reaksjoner - alle andre terapeutiske produkter - for voksne pasienter behandlet med en direkte faktor xa (anl) inhibitor (apixaban eller rivaroxaban) når reversering av antikoagulasjonsbehandling er nødvendig på grunn av livstruende eller ukontrollert blødning.
erivedge 150 mg
orifarm as - vismodegib - kapsel, hard - 150 mg
erivedge 150 mg
2care4 aps - vismodegib - kapsel, hard - 150 mg
erivedge 150 mg
abacus medicine a/s - vismodegib - kapsel, hard - 150 mg
mometason cipla 50 mikrog/ dose
cipla europe nv - mometasonfuroatmonohydrat - nesespray, suspensjon - 50 mikrog/ dose
feksofenadin cipla 120 mg
cipla europe nv - feksofenadinhydroklorid - tablett, filmdrasjert - 120 mg