Latvja - Latvjan - Zāļu valsts aģentūra

sun pharmaceutical industries europe b.v., netherlands - lopinavirum, ritonavirum - apvalkotā tablete - 200 mg/50 mg

Latvja - Latvjan - Zāļu valsts aģentūra

sun pharmaceutical industries europe b.v., netherlands - ciprofloksacīns - apvalkotā tablete - 500 mg

Unjoni Ewropea - Latvjan - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatide - osteoporosis; osteoporosis, postmenopausal - kalcija homeostāze - teriparatide sun is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Latvja - Latvjan - Zāļu valsts aģentūra

teva czech industries s.r.o., czech republic - metoprolola tartrāts - modificētās darbības tablete - 50 mg

Latvja - Latvjan - Zāļu valsts aģentūra

teva czech industries s.r.o., czech republic - metoprolola tartrāts - modificētās darbības tablete - 100 mg

Unjoni Ewropea - Latvjan - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate - cukura diabēts, 2. tips - cukura diabēts - for adult patients with type 2 diabetes mellitus, sitagliptin sun is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. a thiazolidinedione) when use of a pparγ agonist is appropriate and when diet and exercise plus the pparγ agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a pparγ agonist and metformin when use of a pparγ agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin sun is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

Unjoni Ewropea - Latvjan - EMA (European Medicines Agency)

sun pharmaceutical industries (europe) b.v. - ertapenēma nātrijs - bakteriālas infekcijas - ertapenēms - treatmentertapenem sun is indicated in paediatric patients (3 months to 17 years of age) and in adults for the treatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required (see sections 4. 4 un 5. 1):- intra-abdominal infections- community acquired pneumonia- acute gynaecological infections- diabetic foot infections of the skin and soft tissue (see section 4. 4)preventionertapenem sun is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery (see section 4. jāņem vērā oficiālās vadlīnijas par piemērotu izmantot antibakteriālas vielas.

Unjoni Ewropea - Latvjan - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - cukura diabēts, 2. tips - cukura diabēts - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride sun is indicated in combination with a sulphonylurea (i. , triple kombinēto terapiju), kā palīglīdzekli, lai diētu un vingrošanu pacientiem nepietiekami kontrolē par to maksimālā pieļaujama devu metformīns un sulfonilurīnvielas pamata. sitagliptin/metformin hydrochloride sun is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. sitagliptin/metformin hydrochloride sun is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Unjoni Ewropea - Latvjan - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - levetiracetam - epilepsija - citi pretepilepsijas līdzekļi - levetiracetāms saule ir indicēta kā monoterapija daļējas lēkmes lēkmju ārstēšanā ar sekundāru ģeneralizāciju vai bez tās pacientiem no 16 gadu vecuma ar nesen diagnosticētu epilepsiju. levetiracetam saule ir norādīts kā adjunctive terapija): ārstēšana daļēju sākums lēkmju ar vai bez sekundāras vispārināšanas pieaugušajiem un bērniem no četru gadu vecuma slimo ar epilepsiju;ārstēšanā myoclonic lēkmes pieaugušajiem un pusaudžiem no 12 gadu vecuma ar nepilngadīgo myoclonic epilepsija;ārstēšanā galvenais ir vispārēja tonizējoša-clonic lēkmes pieaugušajiem un pusaudžiem no 12 gadu vecuma ar ģeneralizēta idiopātiska epilepsija. levetiracetam saule koncentrāts ir alternatīva pacientiem, kad iekšķīgi ir uz laiku nav iespējams.

Unjoni Ewropea - Latvjan - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - temozolomide - glioma; glioblastoma - antineoplastiski līdzekļi - temozolomide saule ir indicēts, lai ārstētu:pieaugušiem pacientiem ar jaunatklātiem glioblastoma multiforme kopā ar staru terapijas (rt) un pēc tam kā monotherapy apstrāde;bērniem vecumā no trīs gadiem, pusaudžiem un pieaugušiem pacientiem ar ļaundabīgiem glioma, piemēram, glioblastoma multiforme vai anaplastic astrocytoma, parādot atkārtošanās vai progresēšanu pēc tam, kad standarta terapija.