الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
sugammadex mylan
mylan ireland limited - sugammadex sodium - taugakerfi - Öll önnur lækningavörur - 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.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
sugammadex fresenius kabi
fresenius kabi deutschland gmbh - sugammadex sodium - taugakerfi - Öll önnur lækningavörur - 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.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
sugammadex amomed
aop orphan pharmaceuticals gmbh - sugammadex sodium - taugakerfi - Öll önnur lækningavörur - afturköllun taugavöðvablokkunar sem valdið er af rócuronium eða vecuronium. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
sugammadex piramal
piramal critical care b.v. - sugammadex sodium - taugakerfi - sugammadex - reversal of neuromuscular blockade induced by rocuronium or vecuronium in adults.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
sugammadex adroiq
extrovis eu ltd. - sugammadex sodium - taugakerfi - Öll önnur lækningavörur - 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.
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
sugammadex hameln stungulyf, lausn 100 mg/ml
hameln pharma gmbh - sugammadex sodium - stungulyf, lausn - 100 mg/ml
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
caprelsa
sanofi b.v. - vandetanib - skjaldkirtilsæxli - Æxlishemjandi og ónæmismælandi lyf - meðferð er ætlað fyrir meðferð árásargjarn og einkennum sjúklingunum skjaldkirtilskrabbamein (mtc) í sjúklinga með unresectable staðnum háþróaður eða sjúklingum sjúkdómur. meðferð er ætlað í fullorðnir, börn og unglingar á aldrinum 5 ára og eldri. fyrir sjúklinga í hvern aftur komið-á-innleiðsla(sm) stökkbreytingu er ekki vitað eða er neikvæð, hugsanlega neðri gagnast ætti að taka með í reikninginn áður en einstaka meðferð ákvörðun.
الاتحاد الأوروبي -
الأيسلاندية -
EMA (European Medicines Agency)
nexobrid
mediwound germany gmbh - proteolytic enzymes enriched in bromelain - debridement - undirbúningur til meðferðar á sár og sár - nexobrid er ætlað til að fjarlægja eschar hjá fullorðnum með djúpum hluta og fullum þykktumbruna.
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
vetmedin vet. (pimovita) tuggutafla 1,25 mg
boehringer ingelheim vetmedica gmbh* - pimobendanum inn - tuggutafla - 1,25 mg
أيسلندا -
الأيسلاندية -
LYFJASTOFNUN (Icelandic Medicines Agency)
vetmedin vet. (pimovita) tuggutafla 10 mg
boehringer ingelheim vetmedica gmbh* - pimobendanum inn - tuggutafla - 10 mg