Den Europæiske Union - dansk - EMA (European Medicines Agency)

biocryst - peramivir - influenza, human - antivirale midler til systemisk anvendelse - alpivab er indiceret til behandling af ukompliceret influenza hos voksne og børn fra 2 år.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

laboratorios syva, s.a.u. - inaktiverede bluetongue virus, serotype 1, stamme alg2006/01 e1, inaktiveret, bluetongue virus, serotype 4, stamme btv-4/spa-1/2004, inaktiveret, bluetongue virus, serotype 8, stamme bel2006/01 - inaktiverede viral vacciner - cattle; sheep - til aktiv immunisering af får for at forhindre viraemia og reducere kliniske tegn og læsioner forårsaget af bluetongue virus serotyper 1, og/eller 8, og/eller at reducere viraemia* og kliniske tegn og læsioner forårsaget af bluetongue virus serotype 4for aktiv immunisering af kvæg for at forhindre viraemia forårsaget af bluetongue virus serotyper 1, og/eller 8, og/eller at reducere viraemia* forårsaget af bluetongue virus serotype 4.

Danmark - dansk - SEGES Landbrug & Fødevarer

bayer a/s - mefenpyr-diethyl, mefenpyr, iodosulfuron-methyl-na, iodosulfuron, mesosulfuron-methyl, mesosulfuron - vanddispergerbart granulat - 90 g/kg mefenpyr-diethyl ; (~ 76,5 g/kg mefenpyr ; 6 g/kg iodosulfuron-methyl-na ; (~ 5,59 g/kg iodosulfuron ; 30 g/kg mesosulfuron-methyl ; (~ 29,2 g/kg mesosulfuron

Danmark - dansk - SEGES Landbrug & Fødevarer

bayer a/s - mefenpyr-diethyl, mefenpyr, iodosulfuron-methyl-na, iodosulfuron, mesosulfuron-methyl, mesosulfuron - od-formulering - 30 g/l mefenpyr-diethyl ; (~ 25,5 g/l mefenpyr) ; 2 g/l iodosulfuron-methyl-na ; (~ 1,86 g/l iodosulfuron) ; 10 g/l mesosulfuron-methyl ; (~ 9,72 g/l mesosulfuron)

Den Europæiske Union - dansk - EMA (European Medicines Agency)

elanco gmbh - puk-spdv-poly2#1 dna-plasmid, der koder for laks bugspytkirtlen sygdom virus proteiner - immunologicals for atlantisk laks, - atlanterhavslaks - for den aktive immunisering af atlantisk laks til at reducere nedsat daglig vægt gevinst, og reducere dødelighed, hjerte -, pancreas-og skeletmuskulatur læsioner forårsaget af bugspytkirtlen sygdom som følge af infektion med laksefisk alphavirus subtype 3 (sav3).

Danmark - dansk - SEGES Landbrug & Fødevarer

3a kemi a/s - mefenpyr-diethyl, mefenpyr, iodosulfuron-methyl-na, iodosulfuron, mesosulfuron-methyl, mesosulfuron - vanddispergerbart granulat - 90 g/kg mefenpyr-diethyl ; (~ 76,5 g/kg mefenpyr ; 6 g/kg iodosulfuron-methyl-na ; (~ 5,59 g/kg iodosulfuron ; 30 g/kg mesosulfuron-methyl ; (~ 29,2 g/kg mesosulfuron

Den Europæiske Union - dansk - EMA (European Medicines Agency)

intervet international bv - azaglynafarelin - hypofysiske og hypotalamiske hormoner og analoger - dogs; salmonidae (salmonid fish) - kvindelige laksefisk fisk som laks (salmo salar), regnbueørred (oncorhynchus mykiss), havørred (salmo trutta) og fjeldørred (salvelinus alpinus)induktion og synkronisering af ægløsning til produktion af eyed-æg og yngel. hunde (tæver)forebyggelse af gonadal funktion i tæver via langsigtede blokade af gonadotrophin syntese.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

pharmaq as - aeromonas salmonicida (al 2017), vibrio anguillarum serovar o1 (al 112), vibrio anguillarum serovar o2 (al 104) - injektionsvæske, emulsion - akvakultur-dyr (f.eks. fisk )

Den Europæiske Union - dansk - EMA (European Medicines Agency)

pfizer europe ma eeig - crizotinib - carcinom, ikke-småcellet lunge - antineoplastiske midler - xalkori as monotherapy is indicated for:the first‑line treatment of adults with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with previously treated anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with ros1‑positive advanced non‑small cell lung cancer (nsclc)the treatment of paediatric patients (age ≥6 to.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

novartis europharm limited - eltrombopag - purpura, trombocytopenisk, idiopatisk - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 og 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 og 5. revolade is indicated in adult patients with chronic hepatitis c virus (hcv) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy (see sections 4. 4 and 5. revolade is indicated in adult patients with acquired severe aplastic anaemia (saa) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for haematopoietic stem cell transplantation (see section 5.