Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

adoh b.v. - lidocain, tetracain - creme - 70 mg/g+70 mg/g

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

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, mercaptobenzothiazol, methylchlorisothiazolinon, methylparahydroxybenzoat, morpholinylmercaptobenzothiazol, n-cyclohexyl-n-phenylparaphenylendiamin, n-hydroxymethylsuccinimid, n-isopropyl-n-phenylparaphenylendiamin, n,n-diphenylparaphenylendiamin, neomycinsulfat, nikkelsulfat, p-tert butylphenol formaldehyd harpiks, paraphenylendiamin, perubalsam, propylparahydroxybenzoat, quaternium-15, tetracainhydrochlorid, tetramethylthiurammonosulfid, thiomersal, thiram, zinkdibutyldithiocarbamat, zinkdiethyldithiocarbamat - plaster til provokationstest

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

eurocept international b.v. - lidocain, tetracain - medicinsk plaster - 70+70 mg

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

sanofi pasteur - chimeric yellow fever dengue virus serotype 1 (live, attenuated), chimeric yellow fever dengue virus serotype 2 (live, attenuated), chimeric yellow fever dengue virus serotype 3 (live, attenuated), chimeric yellow fever dengue virus serotype 4 (live, attenuated) - dengue - vacciner - dengvaxia is indicated for the prevention of dengue disease caused by dengue virus serotypes 1, 2, 3 and 4 in individuals 6 to 45 years of age with test-confirmed previous dengue infection (see sections 4. 2, 4. 4 og 4. brug af dengvaxia bør være i overensstemmelse med de officielle anbefalinger.

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

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - dengue - vacciner - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

smartpractice denmark aps - alfa-amylcinnamaldehyd, almindelig slåenlav (evernia prunastri), bacitracin, benzocain, benzylparahydroxybenzoat, bronopol, budesonid, butylparahydroxybenzoat, cinnamaldehyd, cinnamylalkohol, clioquinol, cyclohexylbenzothiazylsulfenamid, diazolidinyl urea, dibenzothiazyldisulfid, dipentamethylenthiuramdisulfid, diphenylguanidin, disperse blue 106, disulfiram, epoxyresin, ethylendiamindihydrochlorid, ethylparahydroxybenzoat, eugenol, geraniol, guldnatriumthiosulfat, hydrocortisonbutyrat, hydroxycitronellal, imidurea, isoeugenol, kaliumdichromat, koboltchlorid, kolofonium, lanolinalkohol, mercaptobenzothiazol, methylchlorisothiazolinon, methyldibromoglutharonitrile, methylparahydroxybenzoat, morpholinylmercaptobenzothiazol, n-cyclohexyl-n-phenylparaphenylendiamin, n-hydroxymethylsuccinimid, n-isopropyl-n-phenylparaphenylendiamin, n,n-diphenylparaphenylendiamin, neomycinsulfat, nikkelsulfat, p-tert butylphenol formaldehyd harpiks, paraphenylendiamin, parthenolid, perubalsam, propylparahydroxybenzoat, quaternium-15, tetracainhydrochlorid, tetramethylthiurammonosulfid, thiomersal, thiram, tixocortolpivalat, zinkdibutyldithiocarbamat, zinkdiethyldithiocarbamat - plaster til provokationstest

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

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 23f - pneumococcal infections; immunization - vacciner - aktiv immunisering til forebyggelse af invasiv sygdom, lungebetændelse og akut otitismedium forårsaget af streptococcus pneumoniae hos spædbørn, børn og unge fra 6 uger til 17 år. aktiv immunisering til forebyggelse af invasiv sygdom forårsaget af streptococcus pneumoniae i voksne ≥18 år og ældre. se afsnit 4. 4 og 5. 1 for information om beskyttelse mod specifikke pneumokokserotyper. brug af prevenar 13 bør fastsættes på grundlag af de officielle anbefalinger under hensyntagen til risikoen for invasiv sygdom i forskellige aldersgrupper, underliggende co-morbiditet samt variation af serotype epidemiologi i forskellige geografiske områder.

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

pacira ireland limited - bupivacaine - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

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

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneumokokinfektioner - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. se afsnit 4. 4 og 5. 1 for information om beskyttelse mod specifikke pneumokokserotyper. the use of vaxneuvance should be in accordance with official recommendations.

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

glaxosmithkline biologicals s.a. - split influenza virus inaktiveret, der indeholder antigen svarende til a / california / 07/2009 (h1n1) -afledt stamme anvendt nymc x-179a - influenza, human; immunization; disease outbreaks - influenzavacciner - profylakse af influenza forårsaget af a (h1n1) v 2009 virus. pandemrix bør kun anvendes, hvis de anbefalede årlige trivalente / quadrivalente influenzavacciner ikke er tilgængelige, og hvis immunisering mod (h1n1) v anses for nødvendigt (se afsnit 4. 4 og 4. pandemrix bør anvendes i overensstemmelse med officielle retningslinjer.