VeraSeal Europska Unija - švedski - EMA (European Medicines Agency)

veraseal

instituto grifols, s.a. - humant fibrinogen, humant trombin - hemostas, kirurgisk - hemostatika - stödjande behandling hos vuxna där vanliga kirurgiska tekniker är otillräckliga för förbättring av haemostasisas sutur stöd i kärlkirurgi.

Arti-Cell Forte Europska Unija - švedski - EMA (European Medicines Agency)

arti-cell forte

boehringer ingelheim vetmedica gmbh - kondrogen inducerad häst allogen perifert blod-härrör mesenkymala stamceller - andra droger för sjukdomar i muskel-skelettsystemet - hästar - minskning av mild till måttlig återkommande hälta i samband med icke-septisk ledinflammation hos häst.

Vaxchora Europska Unija - švedski - EMA (European Medicines Agency)

vaxchora

bavarian nordic a/s - vibrio cholerae, stam cvd-103-hgr, live - kolera - vacciner - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. detta vaccin ska användas i enlighet med officiella rekommendationer.

Neptra Europska Unija - švedski - EMA (European Medicines Agency)

neptra

bayer animal health gmbh - florfenikol, hydroklorid terbinafin, mometason furoate - otologicals, kortikosteroider och antiinfectives i kombination - hundar - för behandling av akut hund extern otit eller akut försämring av återkommande öroninflammationer orsakade av blandade infektioner av känsliga stammar av bakterier känsliga för florfenikol (staphylococcus pseudintermedius) och svampar är känsliga för terbinafin (malassezia pachydermatis).

Leqvio Europska Unija - švedski - EMA (European Medicines Agency)

leqvio

novartis europharm limited - inclisiran - hypercholesterolemia; dyslipidemias - lipidmodifierande medel - leqvio is indicated in adults with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia, as an adjunct to diet:in combination with a statin or statin with other lipid-lowering therapies in patients unable to reach ldl-c goals with the maximum tolerated dose of a statin, oralone or in combination with other lipid-lowering therapies in patients who are statin-intolerant, or for whom a statin is contraindicated.

Innovax-ND-ILT Europska Unija - švedski - EMA (European Medicines Agency)

innovax-nd-ilt

intervet international b.v. - cell-associated live recombinant turkey herpesvirus (strain hvt/ndv/ilt) expressing the fusion protein of newcastle disease virus and the glycoproteins gd and gi of infectious laryngotracheitis virus - immunologicals för aves - embryonated chicken eggs; chicken - for active immunisation of one-day-old chicks or embryonated chicken eggs:to reduce mortality and clinical signs caused by newcastle disease (nd) virus,to reduce mortality, clinical signs and lesions caused by avian infectious laryngotracheitis (ilt) virus and marek’s disease (md) virus.

Evrysdi Europska Unija - švedski - EMA (European Medicines Agency)

evrysdi

roche registration gmbh  - risdiplam - muskelatrofi, ryggrad - andra droger för sjukdomar i muskel-skelettsystemet - evrysdi is indicated for the treatment of 5q spinal muscular atrophy (sma) in patients with a clinical diagnosis of sma type 1, type 2 or type 3 or with one to four smn2 copies.

Sugammadex Mylan Europska Unija - švedski - EMA (European Medicines Agency)

sugammadex mylan

mylan ireland limited - sugammadex sodium - neuromuskulär blockade - alla andra terapeutiska produkter - reversal of neuromuscular blockade induced by   rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Amomed Europska Unija - švedski - EMA (European Medicines Agency)

sugammadex amomed

aop orphan pharmaceuticals gmbh - sugammadex sodium - neuromuskulär blockade - alla andra terapeutiska produkter - reversering av neuromuskulär blockad som induceras av rocuronium eller vekuronium. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Sugammadex Piramal Europska Unija - švedski - EMA (European Medicines Agency)

sugammadex piramal

piramal critical care b.v. - sugammadex sodium - neuromuskulär blockade - sugammadex - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.