Letônia - letão - Zāļu valsts aģentūra

mylan pharmaceuticals limited, ireland - bimatoprostum, timololum - acu pilieni, šķīdums - 0,3 mg/5 mg/ml

União Europeia - letão - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - ivacaftor, tezacaftor, elexacaftor - cistiskā fibroze - other respiratory system products - kaftrio is indicated in a combination regimen with ivacaftor for the treatment of cystic fibrosis (cf) in patients aged 6 years and older who have at least one f508del mutation in the cystic fibrosis transmembrane conductance regulator (cftr) gene.

União Europeia - letão - EMA (European Medicines Agency)

aimmune therapeutics ireland limited - defatted powder of arachis hypogaea l., semen (peanuts) - peanut hypersensitivity - allergens - palforzia is indicated for the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. palforzia may be continued in patients 18 years of age and older. palforzia should be used in conjunction with a peanut-avoidant diet.

União Europeia - letão - EMA (European Medicines Agency)

tmc pharma (eu) limited - fosdenopterin hydrobromide dihydrate - metal metabolism, inborn errors - citas gremošanas trakta un metabolisma produkti, - nulibry is indicated for the treatment of patients with molybdenum cofactor deficiency (mocd) type a.

União Europeia - letão - EMA (European Medicines Agency)

proveca pharma limited - glikopironija bromīds - sialorrhea - narkotikas funkcionāliem kuņģa-zarnu trakta traucējumiem - simptomātiska smaga sialojai (hroniska patoloģiska atkailināšanās) ārstēšana bērniem un pusaudžiem vecumā no 3 gadiem ar hroniskām neiroloģiskām slimībām.

União Europeia - letão - EMA (European Medicines Agency)

novartis europharm limited - dabrafenib mesilate - melanoma - antineoplastiski līdzekļi - melanomadabrafenib as monotherapy or in combination with trametinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutation (see sections 4. 4 un 5. palīgvielu attieksmi pret melanomadabrafenib kopā ar trametinib ir norādīts palīgvielu ārstēšanai pieaugušiem pacientiem ar iii stadijā melanomas ar braf v600 mutācijas, pēc pilnīgas rezekcija. non-small cell lung cancer (nsclc)dabrafenib in combination with trametinib is indicated for the treatment of adult patients with advanced non-small cell lung cancer with a braf v600 mutation.

União Europeia - letão - EMA (European Medicines Agency)

vertex pharmaceuticals (ireland) limited - tezacaftor, ivacaftor - cistiskā fibroze - other respiratory system products - 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.

União Europeia - letão - EMA (European Medicines Agency)

akcea therapeutics ireland limited - volanesorsen nātrija - i tipa hiperlipoproteinēmija - citi seruma lipīdus modificējošie līdzekļi - waylivra ir norādīts kā palīglīdzekli, lai uzturs pieaugušiem pacientiem ar ģenētiski apstiprināja, ģimenes chylomicronemia sindroms (fcs) un augsta riska pankreatīts, kuriem atbildes reakcija uz uzturu, un pazeminot triglicerīdu terapija ir bijusi nepietiekama.

União Europeia - letão - EMA (European Medicines Agency)

jazz pharmaceuticals ireland limited - cannabidiol - lennox gastaut syndrome; epilepsies, myoclonic - antiepileptics, - epidyolex ir norādīti izmantot kā adjunctive terapijas konfiskāciju, kas saistīts ar lennox gastaut sindroma (lgs) vai dravet sindroms (ds), kopā ar klobazāms, pacientiem 2 gadu vecuma un vecāki.

União Europeia - letão - EMA (European Medicines Agency)

novartis europharm limited  - siponimod fumārskābe - multiplā skleroze, recidivējoši-pārskaitot - selective immunosuppressants - mayzent ir norādīts ārstēšanai pieaugušiem pacientiem ar sekundāru pakāpeniski multiplā skleroze (spms) ar aktīvo slimību pierāda ar recidīviem vai attēlveidošanas funkcijas iekaisuma aktivitāte.