Onytec 80 mg/g medicinsk neglelak Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

onytec 80 mg/g medicinsk neglelak

orifarm a/s - ciclopirox - medicinsk neglelak - 80 mg/g

Onytec 80 mg/g medicinsk neglelak Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

onytec 80 mg/g medicinsk neglelak

paranova danmark a/s - ciclopirox - medicinsk neglelak - 80 mg/g

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

idefirix

hansa biopharma ab - imlifidase - desensitization, immunologic; kidney transplantation - immunosuppressiva - idefirix is indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. the use of idefirix should be reserved for patients unlikely to be transplanted under the available kidney allocation system including prioritisation programmes for highly sensitised patients.

Fentanyl Carefarm 12 mikrogram/time depotplastre Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

fentanyl carefarm 12 mikrogram/time depotplastre

orifarm a/s - fentanyl - depotplastre - 12 mikrogram/time

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

bridion

merck sharp & dohme b.v. - sugammadex - neuromuskulær blokade - alle andre terapeutiske produkter - tilbagevendelse af neuromuskulær blokade induceret af rocuronium eller vecuronium. for peadiatric befolkning: sugammadex er kun anbefales til rutinemæssig tilbageførsel af rocuronium-induceret blokade i børn og unge.

Sugammadex "hameln" 100 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sugammadex "hameln" 100 mg/ml injektionsvæske, opløsning

hameln pharma gmbh - sugammadexnatrium - injektionsvæske, opløsning - 100 mg/ml

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

sugammadex mylan

mylan ireland limited - sugammadex sodium - neuromuskulær blokade - alle andre terapeutiske 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 "Teva" 100 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sugammadex "teva" 100 mg/ml injektionsvæske, opløsning

teva b.v. - sugammadexnatrium - injektionsvæske, opløsning - 100 mg/ml

Sugammadex Fresenius Kabi Den Europæiske Union - dansk - EMA (European Medicines Agency)

sugammadex fresenius kabi

fresenius kabi deutschland gmbh - sugammadex sodium - neuromuskulær blokade - alle andre terapeutiske 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 "Noridem" 100 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sugammadex "noridem" 100 mg/ml injektionsvæske, opløsning

noridem enterprises ltd. - sugammadexnatrium - injektionsvæske, opløsning - 100 mg/ml