True Test plaster til provokationstest Dánia - dán - Lægemiddelstyrelsen (Danish Medicines Agency)

true test plaster til provokationstest

smartpractice denmark aps - alfa-amylcinnamaldehyd, almindelig slåenlav (evernia prunastri), benzocain, benzylparahydroxybenzoat, butylparahydroxybenzoat, chlorquinaldol, cinchocainhydrochlorid, cinnamaldehyd, cinnamylalkohol, clioquinol, cyclohexylbenzothiazylsulfenamid, dibenzothiazyldisulfid, dipentamethylenthiuramdisulfid, diphenylguanidin, disulfiram, epoxyresin, ethylendiamindihydrochlorid, ethylparahydroxybenzoat, eugenol, geraniol, hydroxycitronellal, isoeugenol, kaliumdichromat, koboltchlorid, kolofonium, lanolinalkohol, merc - plaster til provokationstest

Dolmatil 400 mg filmovertrukne tabletter Dánia - dán - Lægemiddelstyrelsen (Danish Medicines Agency)

dolmatil 400 mg filmovertrukne tabletter

orifarm a/s - sulpirid - filmovertrukne tabletter - 400 mg

Soliris Európai Unió - dán - EMA (European Medicines Agency)

soliris

alexion europe sas - eculizumab - hemoglobinuri, paroxysmal - immunosuppressiva - soliris er indiceret hos voksne og børn til behandling af:paroksysmal natlig haemoglobinuria (pnh). dokumentation af klinisk fordel er påvist hos patienter med haemolysis med klinisk symptom(er) betegnende for høj sygdomsaktivitet, uanset transfusion historie (se afsnit 5. atypiske hæmolytisk uræmisk syndrom (ahus). soliris er indiceret hos voksne til behandling af:ildfaste generaliseret myasthenia gravis (gmg) i patienter, der er anti-acetylcholin-receptor (achr) antistof-positive (se afsnit 5. neuromyelitis optica spektrum forstyrrelse (nmosd) i patienter, der er anti-aquaporin-4 (aqp4) antistof-positive med en recidiverende forløbet af sygdommen.

Supemtek Európai Unió - dán - EMA (European Medicines Agency)

supemtek

sanofi pasteur - influenza a virus subtype h1n1 haemagglutinin, recombinant, influenza a virus subtype h3n2 haemagglutinin, recombinant, influenza b virus victoria lineage haemagglutinin, recombinant, influenza b virus yamagata lineage haemagglutinin, recombinant - influenza, human - vacciner - supemtek is indicated for active immunization for the prevention of influenza disease in adults. supemtek should be used in accordance with official recommendations.

Epysqli Európai Unió - dán - EMA (European Medicines Agency)

epysqli

samsung bioepis nl b.v. - eculizumab - hemoglobinuri, paroxysmal - immunosuppressiva - epysqli is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). evidence of clinical benefit is demonstrated in patients with haemolysis with clinical symptom(s) indicative of high disease activity, regardless of transfusion history.

Bekemv Európai Unió - dán - EMA (European Medicines Agency)

bekemv

amgen technology (ireland) uc - eculizumab - hemoglobinuri, paroxysmal - immunosuppressiva - bekemv is indicated in adults and children for the treatment of paroxysmal nocturnal haemoglobinuria (pnh). dokumentation af klinisk fordel er påvist hos patienter med haemolysis med klinisk symptom(er) betegnende for høj sygdomsaktivitet, uanset transfusion historie (se afsnit 5.

Campral 333 mg enterotabletter Dánia - dán - Lægemiddelstyrelsen (Danish Medicines Agency)

campral 333 mg enterotabletter

merck sante s.a.s. - acamprosatcalcium - enterotabletter - 333 mg

Campral 333 mg enterotabletter Dánia - dán - Lægemiddelstyrelsen (Danish Medicines Agency)

campral 333 mg enterotabletter

paranova danmark a/s - acamprosatcalcium - enterotabletter - 333 mg

Campral 333 mg enterotabletter Dánia - dán - Lægemiddelstyrelsen (Danish Medicines Agency)

campral 333 mg enterotabletter

orifarm a/s - acamprosatcalcium - enterotabletter - 333 mg

Campral EC 333 mg enterotabletter Dánia - dán - Lægemiddelstyrelsen (Danish Medicines Agency)

campral ec 333 mg enterotabletter

orifarm a/s - acamprosatcalcium - enterotabletter - 333 mg