Sefitude (Quietude) Húðuð tafla 445 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sefitude (quietude) húðuð tafla 445 mg

florealis ehf. - valerian root dry extract (3-6:1), ethanol 70 %(v/v) - húðuð tafla - 445 mg

Harpatinum Mjúkt hylki 225 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

harpatinum mjúkt hylki 225 mg

florealis ehf. - devil´s claw dry extract ethanolic 60% (v/v) (4.4-5.0:1) - mjúkt hylki - 225 mg

Sugammadex Mylan 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.

Sugammadex Piramal 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.

Sugammadex Fresenius Kabi 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.

Sugammadex Amomed 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.

Sugammadex Adroiq 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.

Sugammadex hameln Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sugammadex hameln stungulyf, lausn 100 mg/ml

hameln pharma gmbh - sugammadex sodium - stungulyf, lausn - 100 mg/ml

Tobradex Augndropar, dreifa Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

tobradex augndropar, dreifa

novartis healthcare a/s - dexamethasonum fosfat; tobramycinum inn - augndropar, dreifa

Bridion Evrópusambandið - íslenska - EMA (European Medicines Agency)

bridion

merck sharp & dohme b.v. - sugammadex - taugakerfi - Öll önnur lækningavörur - afturköllun taugavöðvablokkunar sem valdið er af rócuronium eða vecuronium. fyrir peadiatric íbúafjöldi: sugammadex er einungis fyrir lífi viðsnúningur rocuronium völdum umsátur í börn og unglingar.