Eiropas Savienība - latviešu - EMA (European Medicines Agency)

sandoz gmbh - pregabalin - anxiety disorders; epilepsy - antiepileptics, - epilepsypregabalin sandoz gmbh ir norādīts kā adjunctive terapija pieaugušajiem ar daļēju lēkmju ar vai bez sekundāras vispārināšanas. Ģeneralizēta trauksme disorderpregabalin sandoz gmbh ir indicēts, lai ārstētu Ģeneralizēta trauksme (vsd) pieaugušajiem.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

zentiva, k.s. - pregabalin - anxiety disorders; epilepsy - antiepileptics, - neuropathic pain , pregabalin zentiva is indicated for the treatment of peripheral and central neuropathic pain in adults. , epilepsy , pregabalin zentiva is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. , generalised anxiety disorder , pregabalin zentiva is indicated for the treatment of generalised anxiety disorder (gad) in adults.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - ambrisentan - hipertensija, plaušu slimība - antihipertensīvie līdzekļi, - volibris is indicated for treatment of pulmonary arterial hypertension (pah) in adult patients of who functional class (fc) ii to iii, including use in combination treatment (see section 5.  efficacy has been shown in idiopathic pah (ipah) and in pah associated with connective tissue disease. volibris is indicated for treatment of pah in adolescents and children (aged 8 to less than 18 years) of who functional class (fc) ii to iii including use in combination treatment. efficacy has been shown in ipah, familial, corrected congenital and in pah associated with connective tissue disease (see section 5.

Eiropas Savienība - latviešu - EMA (European Medicines Agency)

roche registration limited - emicizumabs - a hemofīlija - antihemorāģija - hemlibra is indicated for routine prophylaxis of bleeding episodes in patients with haemophilia a (congenital factor viii deficiency):with factor viii inhibitorswithout factor viii inhibitors who have:severe disease (fviii < 1%)moderate disease (fviii ≥ 1% and ≤ 5%) with severe bleeding phenotype. hemlibra var izmantot visās vecuma grupās.

Latvija - latviešu - Zāļu valsts aģentūra

b.braun melsungen ag, germany - gelatinum succinas, natrii chloridum, natrii hydroxidum - Šķīdums infūzijām

Latvija - latviešu - Zāļu valsts aģentūra

bausch + lomb ireland limited, ireland - latanoprosts - acu pilieni, šķīdums - 50 μg/ml

Latvija - latviešu - Zāļu valsts aģentūra

medochemie ltd., cyprus - pregabalīns - kapsula, cietā - 150 mg

Latvija - latviešu - Zāļu valsts aģentūra

medochemie ltd., cyprus - pregabalīns - kapsula, cietā - 75 mg

Latvija - latviešu - Zāļu valsts aģentūra

elpen pharmaceutical co. inc (sa), greece - salmeterolum, fluticasoni propionas - inhalācijas pulveris, dozēts - 50 mikrogrami/250 mikrogrami/devā

Latvija - latviešu - Zāļu valsts aģentūra

g.l. pharma gmbh, austria - pregabalīns - kapsula, cietā - 50 mg