Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
dexól saft 3 mg/ml
laboratoria qualiphar - dextromethorphanum hýdróbrómíð mónóhýdrat - saft - 3 mg/ml
Evrópusambandið -
íslenska -
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.
Evrópusambandið -
íslenska -
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.
Evrópusambandið -
íslenska -
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.
Evrópusambandið -
íslenska -
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.
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
dexavit stungulyf/innrennslislyf, lausn 4 mg/ml
vital pharma nordic aps - dexamethasonum natríumfosfat - stungulyf/innrennslislyf, lausn - 4 mg/ml
Evrópusambandið -
íslenska -
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.
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
dexametason abcur tafla 1 mg
abcur ab - dexamethasonum fosfat - tafla - 1 mg
Ísland -
íslenska -
LYFJASTOFNUN (Icelandic Medicines Agency)
dexametason abcur tafla 4 mg
abcur ab - dexamethasonum fosfat - tafla - 4 mg
Evrópusambandið -
íslenska -
EMA (European Medicines Agency)
pramipexole accord
accord healthcare s.l.u. - pramipexól tvíhýdróklóríð einhýdrat - parkinson disease; restless legs syndrome - anti-parkinsonslyf - pramipexole accord er ætlað fullorðnum til meðferðar á einkennum parkinsonsveiki, einkennalaus (án levodopa) eða í samsettri meðferð með levodopa, ég. á meðan á sjúkdómnum stendur, í gegnum seint stig þegar áhrif levódópa berast eða verða ósamræmi og sveiflur á meðferðaráhrifum eiga sér stað (lokaskammtur eða "á-burt" sveiflur).