Denmark - Danish - Lægemiddelstyrelsen (Danish Medicines Agency)

newbury pharmaceuticals ab - icatibant - injektionsvæske, opløsning i fyldt injektionssprøjte - 30 mg

Denmark - Danish - Lægemiddelstyrelsen (Danish Medicines Agency)

glenmark pharmaceuticals s.r.o. - mometasonfuroat monohydrat, olopatadinhydrochlorid - næsespray, suspension - 25+600 mikrog./dosis

European Union - Danish - EMA (European Medicines Agency)

roche registration ltd. - daclizumab - graft rejection; kidney transplantation - immunosuppressiva - zenapax er indiceret til forebyggelse af akut organafstødning i de novo allogen nyre transplantation og skal anvendes samtidig med en immunosuppressive regime, herunder cyclosporin og kortikosteroider i patienter, der ikke er meget vaccineret.

European Union - Danish - EMA (European Medicines Agency)

intervet international b.v. - levende fugleinfektiøs bronkitisvirus, stamme d388 - live viral vaccines, domestic fowl - kylling - til aktiv immunisering af kyllinger for at reducere respiratoriske tegn på aviær infektiøs bronkitis forårsaget af qx-lignende varianter af infektiøs bronkitisvirus.

European Union - Danish - EMA (European Medicines Agency)

roche registration gmbh  - casirivimab, imdevimab - covid-19 virus infection - immune sera og immunoglobuliner, - ronapreve is indicated for:treatment of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19 (see section 4. prevention of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg (see section 4. the use of ronapreve should take into account information on the activity of ronapreve against viral variants of concern. se afsnit 4. 4 og 5.

European Union - Danish - EMA (European Medicines Agency)

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

European Union - Danish - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - regdanvimab - covid-19 virus infection - immune sera og immunoglobuliner, - regdanvimab is indicated for the treatment of adults with coronavirus disease 2019 (covid-19) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

European Union - Danish - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - clopidogrel (as hydrogen sulfate) - stroke; peripheral vascular diseases; myocardial infarction; acute coronary syndrome - antitrombotiske midler - clopidogrel er indiceret hos voksne til forebyggelse af atherothrombotic begivenheder i:- patienter med myokardieinfarkt (fra få dage, indtil der er mindre end 35 dage), iskæmisk slagtilfælde (fra 7 dage indtil mindre end 6 måneder) eller etableret perifer arteriel sygdom. - patienter, der lider af akut koronar syndrom:non-st-segment elevation akut koronar syndrom (ustabil angina pectoris eller non-q-tak myokardieinfarkt), herunder patienter, der gennemgår en stent placering efter perkutan koronar intervention, i kombination med acetylsalicylsyre (asa). st-segment elevation akut myokardieinfarkt, i kombination med asa i medicinsk behandlede patienter, der er berettiget til trombolytisk terapi.

European Union - Danish - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - nivolumab - carcinom, ikke-småcellet lunge - antineoplastiske og immunmodulerende midler, monoklonale antistoffer - nivolumab bms er indiceret til behandling af lokalt avanceret eller metastatisk pladeformet ikke-småcellet lungekræft (nsclc) efter forudgående kemoterapi hos voksne.

European Union - Danish - EMA (European Medicines Agency)

glaxosmithkline trading services limited - sotrovimab - covid-19 virus infection - immune sera og immunoglobuliner, - xevudy is indicated for the treatment of adults and adolescents (aged 12 years and over and weighing at least 40 kg) with coronavirus disease 2019 (covid-19) who do not require oxygen supplementation and who are at increased risk of progressing to severe covid-19.