Zulvac 1 Bovis Unione Europea - islandese - EMA (European Medicines Agency)

zulvac 1 bovis

zoetis belgium sa - óvirkja blátunguveiru, sermigerð 1 - Ónæmisfræðilegar upplýsingar - nautgripir - virkt ónæmisaðgerð nautgripa frá 2½ mánaða aldri til að koma í veg fyrir veirublæði af völdum blátunguveiru, sermisgerð 1. upphaf ónæmis: 15 dögum eftir að grunnbólusetningarferlið er lokið. lengd ónæmis: 12 mánuðir.

Zulvac 1+8 Bovis Unione Europea - islandese - EMA (European Medicines Agency)

zulvac 1+8 bovis

zoetis belgium sa - óvirkt bluetongue veira, serotype 1, álag btv-1/alg2006/01 e1 rp, óvirkur bluetongue veira, serotype 8, álag btv-8/bel2006/02 - bluetongue veira, Ónæmislyf, Ónæmislyf fyrir bovidae, nautgripir, Óvirkur veiru bóluefni - nautgripir - virk ónæmisaðgerð nautgripa frá 3 mánaða aldri til að koma í veg fyrir veirumlækkun vegna blátunguveiru (btv), sermisgerð 1 og 8. * (hjólreiðar gildi (ct) ≥ 36 með fullgiltri rt-pcr aðferð, sem gefur til kynna að ekki sé til staðar veiruþáttur).

Veklury Unione Europea - islandese - EMA (European Medicines Agency)

veklury

gilead sciences ireland uc - remdesivir - covid-19 virus infection - veklury is indicated for the treatment of coronavirus disease 2019 (covid 19) in:adults and paediatric patients (at least 4 weeks of age and weighing at least 3 kg) with pneumonia requiring supplemental oxygen (low- or high-flow oxygen or other non-invasive ventilation at start of treatment)adults and paediatric patients (weighing at least 40 kg) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

Regkirona Unione Europea - islandese - EMA (European Medicines Agency)

regkirona

celltrion healthcare hungary kft. - regdanvimab - covid-19 virus infection - Ónæmiskerfið sera og mótefni, - 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.

Evusheld Unione Europea - islandese - EMA (European Medicines Agency)

evusheld

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

Paxlovid Unione Europea - islandese - EMA (European Medicines Agency)

paxlovid

pfizer europe ma eeig - nirmatrelvir, ritonavir - covid-19 virus infection - paxlovid is indicated for the treatment of coronavirus disease 2019 (covid-19) in adults who do not require supplemental oxygen and who are at increased risk for progressing to severe covid 19.

Okedi Unione Europea - islandese - EMA (European Medicines Agency)

okedi

laboratorios farmacéuticos rovi, s.a. - risperidone - geðklofa - psycholeptics - treatment of schizophrenia in adults for whom tolerability and effectiveness has been established with oral risperidone.

BCG-medac Duft og leysir fyrir þvagblöðrudreifu Islanda - islandese - LYFJASTOFNUN (Icelandic Medicines Agency)

bcg-medac duft og leysir fyrir þvagblöðrudreifu

medac gesellschaft für klinische spezialpräparate gmbh - bcg bacteria - duft og leysir fyrir þvagblöðrudreifu

Baytril vet. Stungulyf, lausn 100 mg/ml Islanda - islandese - LYFJASTOFNUN (Icelandic Medicines Agency)

baytril vet. stungulyf, lausn 100 mg/ml

elanco animal health gmbh - enrofloxacinum inn - stungulyf, lausn - 100 mg/ml