Terbinafin Medical Valley Tafla 250 mg Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

terbinafin medical valley tafla 250 mg

medical valley invest ab - terbinafinum hýdróklóríð - tafla - 250 mg

Salmeterol/Fluticasone Neutec (Salmeterol/Fluticasone Wellnex) Innöndunarduft, afmældir skammtar 50 míkróg/250 míkróg/skammt Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

salmeterol/fluticasone neutec (salmeterol/fluticasone wellnex) innöndunarduft, afmældir skammtar 50 míkróg/250 míkróg/skammt

neutec inhaler ireland limited - salmeterolum xínafóat; fluticasonum própíónat - innöndunarduft, afmældir skammtar - 50 míkróg/250 míkróg/skammt

Norgesic 35 mg/450 mg Tafla 35+450 mg Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

norgesic 35 mg/450 mg tafla 35+450 mg

viatris aps - orphenadrinum cítrat; paracetamolum inn - tafla - 35+450 mg

Salmex Innöndunarduft, afmældir skammtar 50 míkróg/250 míkróg/skammt Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

salmex innöndunarduft, afmældir skammtar 50 míkróg/250 míkróg/skammt

glenmark pharmaceuticals nordic ab* - salmeterolum xínafóat; fluticasonum própíónat - innöndunarduft, afmældir skammtar - 50 míkróg/250 míkróg/skammt

Seretide Innúðalyf, dreifa 25/250 míkróg/skammt Izland - izlandi - LYFJASTOFNUN (Icelandic Medicines Agency)

seretide innúðalyf, dreifa 25/250 míkróg/skammt

glaxosmithkline pharma a/s - salmeterolum xínafóat; fluticasonum própíónat - innúðalyf, dreifa - 25/250 míkróg/skammt

Recarbrio Európai Unió - izlandi - EMA (European Medicines Agency)

recarbrio

merck sharp & dohme b.v.  - imipenem einhýdrat, cílastatín járn, relebactam einhýdrat - gramm-neikvæð bakteríusýkingum - carbapenems, antibacterials for systemic use, - recarbrio is indicated for:- treatment of hospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap), in adults (see sections 4. 4 og 5. - treatment of bacteraemia that occurs in association with, or is suspected to be associated with hap or vap, in adults. - treatment of infections due to aerobic gram-negative organisms in adults with limited treatment options (see sections 4. 2, 4. 4 og 5. Íhuga ætti að opinbera leiðsögn á réttri notkun af sýklalyfjum.

Nplate Európai Unió - izlandi - EMA (European Medicines Agency)

nplate

amgen europe b.v. - romiplostim - purpura, blóðflagnafæð, blóðflagnafæð - antihemorrhagics - adults:nplate is indicated for the treatment of primary immune thrombocytopenia  (itp) in adult patients who are refractory to other treatments (e. barkstera, immúnóglóbúlín). paediatrics:nplate is indicated for the treatment of chronic primary immune thrombocytopenia (itp) in paediatric patients one year of age and older who are refractory to other treatments (e. barkstera, immúnóglóbúlín).