Europese Unie - Deens - EMA (European Medicines Agency)

zoetis belgium sa - modificeret levende svine respiratorisk og reproduktiv syndrom virus - immunologicals for suidae, live viral vaccines - svin - til aktiv immunisering af klinisk raske svin fra 1 dag af alder i en porcine respiratory og reproduktiv syndrom (prrs) - virus forurenet miljøet, at reducere viraemia og nasal kaste forårsaget af infektion med europæisk stammer af prrs-virus (genotype 1). fedtsvin: desuden blev vaccination af seronegative 1-dages gamle grise påvist for signifikant at reducere lungelæsioner mod udfordring indgivet efter 26 uger efter vaccination. vaccination af seronegative 2 uger gamle smågrise blev påvist, at reducere lunge læsioner og mundtlige kaste imod udfordringen administreres på 28 dage, og på 16 uger efter vaccination. gylte og søer: ud, før graviditet vaccination af klinisk raske gylte og søer, enten seropositive eller seronegative, blev påvist, at reducere transplacental infektion forårsaget af prrs-virus i løbet af tredje trimester af graviditeten, og for at mindske den dermed forbundne negative indvirkning på den reproduktive ydeevne (reduktion af forekomst af dødfødsler, grisling viraemia ved fødslen og ved fravænning, af lunge læsioner og viral load i lungerne i smågrise til fravænning).

Europese Unie - Deens - EMA (European Medicines Agency)

pfizer europe ma eeig - gemtuzumab ozogamicin - leukæmi, myeloid, akut - antineoplastiske midler - mylotarg er angivet for kombinationsbehandling med daunorubicin (dnr) og cytarabine (arac) til behandling af patienter, alder 15 år og derover med tidligere ubehandlet, de novo cd33-positive akut myeloid leukæmi (aml), bortset fra akut promyelocyt leukæmi (apl).

Europese Unie - Deens - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - andre antineoplastiske midler - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Europese Unie - Deens - EMA (European Medicines Agency)

paion deutschland gmbh - remimazolam besilate - bevidst sedation - psykoleptika - remimazolam is indicated in adults for procedural sedation. remimazolam 50 mg is indicated in adults for intravenous induction and maintenance of general anaesthesia.

Europese Unie - Deens - EMA (European Medicines Agency)

techdow pharma netherlands b.v.  - enoxaparinnatrium - venøs tromboembolisme - antitrombotiske midler - inhixa er angivet for voksne om:forebyggelse af venøs tromboemboli, især hos patienter, der gennemgår ortopædisk, generelt eller onkologiske kirurgi. forebyggelse af venøs tromboemboli hos patienter, sengeliggende på grund af akut sygdom, herunder akut hjertesvigt, akut respirationssvigt, alvorlige infektioner, samt forværring af reumatiske sygdomme, der forårsager blokering af patienten (gælder for styrker på 40 mg/0. 4 ml). behandling af dyb venøs trombose (dvt), kompliceret eller ukompliceret ved lungeemboli. behandling af ustabil angina og non q bølge myokardieinfarkt, i kombination med acetylsalicylsyre (asa). behandling af akut st-segment elevation myocardial infarction (stemi), herunder patienter, der behandles konservativt eller der vil senere gennemgå perkutan koronar angioplastik (gælder for styrker på 60 mg/0. 6 ml, 80 mg/0. 8 ml og 100 mg/1 ml). blodprop forebyggelse i den ekstrakorporale cirkulation under hæmodialyse.

Europese Unie - Deens - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - hase herpesvirus (f205 stamme) antigener - immunologier til canidae - hunde - aktiv immunisering af tæver for at forebygge dødelighed, kliniske tegn og læsioner hos hvalpe som følge af hundeinfektioner af hundeinfektioner erhvervet i de første par dage af livet.

Europese Unie - Deens - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains) - immunologicals for felidae, - katte - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs. onsets of immunity isone week after primary vaccination course. the duration of immunity is one year after primary vaccination course and three years after the last re-vaccination.

Europese Unie - Deens - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline panleucopenia virus (pli iv) - immunologicals for felidae, - katte - active immunisation of cats aged eight weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs;against feline panleucopenia to prevent mortality and clinical signs. onset of immunity is one week after primary vaccination course the duration of immunity is one year after the primary vaccination course and three years after the last re-vaccination.

Europese Unie - Deens - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated feline panleucopenia virus (pli iv), felv recombinant canarypox virus (vcp97) - immunologicals for felidae, - katte - active immunisation of cats aged 8 weeks and older:against feline viral rhinotracheitis to reduce clinical signs;against calicivirus infection to reduce clinical signs ;against feline panleucopenia to prevent mortality and clinical signs;against leukaemia to prevent persistent viraemia and clinical signs of the related disease. onsets of immunity are 1 week after primary vaccination course for rhinotracheitis, calicivirus and panleucopenia components, and 2 weeks after primary vaccination course for feline leukaemia component. the duration of immunity is one year after the last re-vaccination for the feline leukaemia component, and one year after primary vaccination course and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.

Europese Unie - Deens - EMA (European Medicines Agency)

boehringer ingelheim vetmedica gmbh - attenuated feline rhinotracheitis herpesvirus (fhv f2 strain), inactivated feline calicivirosis antigens (fcv 431 and g1 strains), attenuated chlamydophila felis (905 strain), attenuated feline panleucopenia virus (pli iv) - immunologicals for felidae, - katte - active immunisation of cats aged eight weeks and older:• against feline viral rhinotracheitis to reduce clinical signs;• against calicivirus infection to reduce clinical signs;• against chlamydophila felis infection to reduce clinical signs;• against feline panleucopenia to prevent mortality and clinical signs. immunitetstrin har vist sig en uge efter primærvaccinationskursus for rhinotracheitis, calicivirus, chlamydophila felis og panleucopenia komponenter. the duration of immunity is one year after the last re-vaccination for the chlamydiosis component, and oneyear after primary vaccination and three years after the last re-vaccination for the rhinotracheitis, calicivirosis and panleucopenia components.