Skytrofa (previously Lonapegsomatropin Ascendis Pharma) Den Europæiske Union - dansk - EMA (European Medicines Agency)

skytrofa (previously lonapegsomatropin ascendis pharma)

ascendis pharma endocrinology division a/s - lonapegsomatropin - growth and development - hypofysiske og hypotalamiske hormoner og analoger - growth failure in children and adolescents aged from 3 years up to 18 years due to insufficient endogenous growth hormone secretion (growth hormone deficiency [ghd]),.

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

hexyon

sanofi pasteur europe - filamentous haemagglutinin, haemophilus influenzae type b polysaccharide (polyribosylribitol phosphate), hepatitis b surface antigen, pertussis toxoid, poliovirus (inactivated) type 1 (mahoney strain) produced on vero cells, poliovirus (inactivated) type 2 (mef-1 strain) produced on vero cells, poliovirus (inactivated) type 3 (saukett strain) produced on vero cells, tetanus protein, tetanus toxoid adsorbed on aluminium hydroxide, hydrated, diphtheria toxoid - hepatitis b; tetanus; immunization; meningitis, haemophilus; whooping cough; poliomyelitis; diphtheria - vacciner - hexyon (dtap-ipv-hb-hib) er angivet til primær og booster nødvaccination, som spædbørn og småbørn fra seks uger mod difteri, stivkrampe, kighoste, hepatitis b, polio og invasive sygdomme forårsaget af haemophilus influenzae type b (hib). brug af denne vaccine bør være i overensstemmelse med de officielle anbefalinger.

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

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacciner - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. brug af denne vaccine bør være i overensstemmelse med de officielle anbefalinger.

Spikevax (previously COVID-19 Vaccine Moderna) Den Europæiske Union - dansk - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacciner - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

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

arexvy

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - respiratoriske syncytiale virusinfektioner - vacciner - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. brug af denne vaccine bør være i overensstemmelse med de officielle anbefalinger.

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

advocate

bayer animal health gmbh - imidacloprid, moxidectin - antiparasitiske produkter, insekticider og repellenter - dogs; cats; ferrets - dogsfor hunde, der lider af, eller er i risiko fra, blandet parasitære infektioner:behandling og forebyggelse af loppeangreb (ctenocephalides felis),behandling af bidende lus (trichodectes canis),behandling af øre-mide angrebets (otodectes cynotis), sarcoptic mange (forårsaget af sarcoptes scabiei var. canis), demodicosis (forårsaget af demodex canis),forebyggelse af sygdom hjerteorm (l3 og l4-larver af dirofilaria immitis),behandling af cirkulerende microfilariae (dirofilaria immitis),behandling af kutane dirofilariosis (voksne stadier af dirofilaria repens)forebyggelse af kutan dirofilariosis (l3 larver af dirofilaria repens),reduktion af cirkulerende microfilariae (dirofilaria repens),forebyggelse af angiostrongylosis (l4-larver og umodne voksne af angiostrongylus vasorum),behandling af angiostrongylus vasorum og crenosoma vulpis,forebyggelse af spirocercosis (spirocerca lupi),behandling af eucoleus (syn. capillaria) boehmi (voksne),behandling af øjet orm thelazia callipaeda (voksne),behandling af infektioner med mave-nematoder (l4-larver, umodne og voksne af toxocara canis, ancylostoma caninum og uncinaria stenocephala, voksne af toxascaris leonina og trichuris vulpis). produktet kan bruges som en del af en behandlingsstrategi for loppe allergi dermatitis (fad). catsfor katte, der lider af, eller er i risiko fra, blandet parasitære infektioner:behandling og forebyggelse af loppeangreb (ctenocephalides felis),behandling af øre-mide angrebets (otodectes cynotis),behandling af notoedric sukkerærter (notoedres cati),behandling af lungworm eucoleus aerophilus (syn. capillaria aerophila) (voksne),forebyggelse af lungworm sygdom (l3/l4-larver af aelurostrongylus abstrusus),behandling af lungworm aelurostrongylus abstrusus (voksne),behandling af øjet orm thelazia callipaeda (voksne),forebyggelse af sygdom hjerteorm (l3 og l4-larver af dirofilaria immitis),behandling af infektioner med mave-nematoder (l4-larver, umodne og voksne af toxocara cati og ancylostoma tubaeforme). produktet kan bruges som en del af en behandlingsstrategi for loppe allergi dermatitis (fad). ferretsfor fritter, der lider af, eller er i risiko fra, blandet parasitære infektioner:behandling og forebyggelse af loppeangreb (ctenocephalides felis),forebyggelse af sygdom hjerteorm (l3 og l4-larver af dirofilaria immitis).

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

suprelorin

virbac s.a. - deslorelinacetat - hypofysiske og hypotalamiske hormoner og analoger - dogs; ferrets - til induktion af midlertidig infertilitet hos raske, hele, seksuelt modne hundehunde og fritter.

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

vectormune nd

ceva-phylaxia co. ltd. - celleassocieret levende rekombinant kalkunherpesvirus (rhvt / nd), der udtrykker fusionsproteinet af newcastle disease-virus-d-26-lentogen stamme - immunologicals for aves, live viral vacciner - chicken; embryonated eggs - til aktiv immunisering af 18 dage gamle befrugtede æg eller en-dage gamle kyllinger til at reducere dødelighed og kliniske tegn forårsaget af newcastle disease virus og til at reducere dødeligheden, kliniske tegn og læsioner forårsaget af marek ' s disease virus med en fænotype, der er "fremme i skoene".

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

kolbam

retrophin europe ltd - cholsyre - metabolisme, infødte fejl - galde og lever terapi - cholic syre fgk er indiceret til behandling af medfødte fejl af primær galdesyre syntese, i spædbørn fra én måneds alder til kontinuerlig livslang behandling gennem voksenalderen, omfatter følgende enkelt enzym fejl:sterol-27-hydroxylase (fremlægger som cerebrotendinous xanthomatosis, ctx) mangel;2- (eller alpha-) methylacyl-coa racemase (amacr) mangel;kolesterol 7 alfa-hydroxylase (cyp7a1) - mangel.

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

teslascan

ge healthcare as - mangafodipir trinatrium - mr scanning - kontrastmedier - dette lægemiddel er kun til diagnostisk brug. kontrastmiddel til diagnostisk magnetisk resonans imaging (mri) til påvisning af læsioner i leveren, der mistænkes for at være på grund af metastatisk sygdom eller hepatocellulært karcinom. som et supplement til mr-at en støtte i undersøgelsen af fokale læsioner i bugspytkirtlen.