Eksemestan Intas 25 mg filmsko obložene tablete Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

eksemestan intas 25 mg filmsko obložene tablete

intas pharmaceuticals limited - eksemestan - filmsko obložena tableta - eksemestan 25 mg / 1 tableta - eksemestan

Eksemestan Intas 25 mg filmsko obložene tablete Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

eksemestan intas 25 mg filmsko obložene tablete

intas pharmaceuticals limited - eksemestan - filmsko obložena tableta - eksemestan 25 mg / 1 tableta - eksemestan

Eksemestan Intas 25 mg filmsko obložene tablete Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

eksemestan intas 25 mg filmsko obložene tablete

intas pharmaceuticals limited - eksemestan - filmsko obložena tableta - eksemestan 25 mg / 1 tableta - eksemestan

Eksemestan Intas 25 mg filmsko obložene tablete Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

eksemestan intas 25 mg filmsko obložene tablete

intas pharmaceuticals limited - eksemestan - filmsko obložena tableta - eksemestan 25 mg / 1 tableta - eksemestan

Eksemestan Intas 25 mg filmsko obložene tablete Slovenia - Kislovenia - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

eksemestan intas 25 mg filmsko obložene tablete

intas pharmaceuticals limited - eksemestan - filmsko obložena tableta - eksemestan 25 mg / 1 tableta - eksemestan

Kalydeco Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

kalydeco

vertex pharmaceuticals (ireland) limited - ivacaftor - cistična fibroza - drugi proizvodi dihal - kalydeco tablets are indicated:as monotherapy for the treatment of adults, adolescents, and children aged 6 years and older and weighing 25 kg or more with cystic fibrosis (cf) who have an r117h cftr mutation or one of the following gating (class iii) mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: g551d, g1244e, g1349d, g178r, g551s, s1251n, s1255p, s549n or s549r (see sections 4. 4 in 5. in a combination regimen with tezacaftor/ivacaftor tablets for the treatment of adults, adolescents, and children aged 6 years and older with cystic fibrosis (cf) who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cftr gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t. in a combination regimen with ivacaftor/tezacaftor/elexacaftor tablets for the treatment of adults, adolescents, and children aged 6 years and older with cystic fibrosis (cf) who have at least one f508del mutation in the cftr gene (see section 5. kalydeco granules are indicated for the treatment of infants aged at least 4 months, toddlers and children weighing 5 kg to less than 25 kg with cystic fibrosis (cf) who have an r117h cftr mutation or one of the following gating (class iii) mutations in the cftr gene: g551d, g1244e, g1349d, g178r, g551s, s1251n, s1255p, s549n or s549r (see sections 4. 4 in 5. in a combination regimen with ivacaftor/tezacaftor/elexacaftor for the treatment of cystic fibrosis (cf) in paediatric patients aged 2 to less than 6 years who have at least one f508del mutation in the cftr gene.

Orkambi Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

orkambi

vertex pharmaceuticals (ireland) limited - lumacaftor, ivacaftor - cistična fibroza - drugi proizvodi dihal - orkambi tablete so primerna za zdravljenje cistična fibroza (cf) pri bolnikih, starih 6 let in več, ki so homozygous za f508del mutacije v cftr gena. orkambi granules are indicated for the treatment of cystic fibrosis (cf) in children aged 1 year and older who are homozygous for the f508del mutation in the cftr gene.

Symkevi Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

symkevi

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - cistična fibroza - drugi proizvodi dihal - symkevi is indicated in a combination regimen with ivacaftor tablets for the treatment of patients with cystic fibrosis (cf) aged 6 years and older who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t.

Zavicefta Umoja wa Ulaya - Kislovenia - EMA (European Medicines Agency)

zavicefta

pfizer ireland pharmaceuticals - avibactam sodium, ceftazidime pentahydrate - pneumonia, bacterial; soft tissue infections; pneumonia; urinary tract infections; gram-negative bacterial infections - antibacterials za sistemsko uporabo, - zavicefta is indicated in adults and paediatric patients aged 3 months and older for the treatment of the following infections:complicated intra-abdominal infection (ciai)complicated urinary tract infection (cuti), including pyelonephritishospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap)treatment of patients with bacteraemia that occurs in association with, or is suspected to be associated with, any of the infections listed above. zavicefta is also indicated for the treatment of infections due to aerobic gram-negative organisms in adults and paediatric patients aged 3 months and older with limited treatment options. upoštevati je treba uradne smernice za ustrezno uporabo protibakterijsko agenti.