technescan dtpa (vezi v09ea01)
mallinckrodt medical b.v. - olanda - tc 99 m - acid pentetic - kit pentru produs radiofarmaceutic - 20,8mg - aparat renal compusi cu technetium tc99
technescan dmsa 1,2 mg
mallinckrodt medical bv. - olanda - tc 99 m - acid succinic dirmercopto - kit pt. preparat radiofarmaceutic - 1,2mg - aparat renal compusi cu technetium tc99
technescan dtpa (vezi v09ea01)
mallinckrodt medical b.v. - olanda - tc 99m - acid pentetic - trusa (kit) pt. preparate radiofarmaceutice - 20,8mg - aparat renal compusi cu technetium tc99
technescan dmsa 1,2 mg
curium netherlands b.v. - olanda - tc 99m - acid dirmercopto succinic - kit pt. preparat radiofarmaceutic - 1,2mg - aparat renal compusi cu technetium tc99
vincamin-bp 7,5 mg/ml soluţie injectabilă
sc balkan pharmaceuticals srl - vincaminum - soluţie injectabilă - 7,5 mg/ml
vincamina 10 mg
biofarm s.a. - romania - vincaminum - draj. - 10mg - vasodilatatoare periferice alte vasodilatatoare periferice
mepivacaina normogen 30 mg/ml
laboratorios normon s.a. - spania - mepivacainum - sol. inj. - 30mg/ml - anestezice locale amide
vincamină-bp 7,5 mg/ml soluţie injectabilă
sc balkan pharmaceuticals srl - vincaminum - soluţie injectabilă - 7,5 mg/ml
vincamina drajeuri 10 mg
biofarm sa, sc - vincaminum - drajeuri - 10 mg
kalydeco
vertex pharmaceuticals (ireland) limited - ivacaftor - fibroză chistică - alte produse ale sistemului respirator - 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 și 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 și 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.