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 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.

Ertapenem SUN Evrópusambandið - íslenska - EMA (European Medicines Agency)

ertapenem sun

sun pharmaceutical industries (europe) b.v. - natríum ertapenem - bakteríusýkingar - ertapenem - treatmentertapenem sun is indicated in paediatric patients (3 months to 17 years of age) and in adults for the treatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required (see sections 4. 4 og 5. 1):- intra-abdominal infections- community acquired pneumonia- acute gynaecological infections- diabetic foot infections of the skin and soft tissue (see section 4. 4)preventionertapenem sun is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery (see section 4. Íhuga ætti að opinbera leiðsögn á réttri notkun af sýklalyfjum.

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.

Sitagliptin Sandoz Filmuhúðuð tafla 100 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sitagliptin sandoz filmuhúðuð tafla 100 mg

sandoz a/s* - sitagliptinum hýdróklóríð - filmuhúðuð tafla - 100 mg

Sitagliptin Zentiva Filmuhúðuð tafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sitagliptin zentiva filmuhúðuð tafla 50 mg

zentiva k.s.* - sitagliptinum hýdróklóríð - filmuhúðuð tafla - 50 mg

Sitagliptin/Metformin Krka Filmuhúðuð tafla 50 mg/1000 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

sitagliptin/metformin krka filmuhúðuð tafla 50 mg/1000 mg

krka, d.d., novo mesto - sitagliptinum inn; metforminum hýdróklóríð - filmuhúðuð tafla - 50 mg/1000 mg