União Europeia - letão - EMA (European Medicines Agency)

gilead sciences ireland uc - elvitegravir, cobicistat, emtricitabine, tenofovir disoproxil fumarate - hiv infekcijas - antivirals for treatment of hiv infections, combinations, antivirals for systemic use - Ārstēšana ar cilvēka imūndeficīta vīrusu (hiv 1) 1 infekcijas pieaugušajiem vecumā no 18 gadiem un virs kurš ir antiretrovirālo ārstēšanu-naivi vai ir inficēti ar hiv 1 bez zināmas mutācijas, kas saistītas ar rezistenci pret jebkuru no trim pretretrovīrusu aģentu stribild.

União Europeia - letão - EMA (European Medicines Agency)

viiv healthcare bv - dolutegravir - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of human immunodeficiency virus (hiv) infected adults, adolescents and children of at least 6 years of age or older and weighing at least 14 kg. tivicay is indicated in combination with other anti-retroviral medicinal products for the treatment of human immunodeficiency virus (hiv) infected adults, adolescents and children of at least 4 weeks of age or older and weighing at least 3 kg.

União Europeia - letão - EMA (European Medicines Agency)

merck sharp dohme ltd - boceprevīrs - c hepatīts, hronisks - pretvīrusu līdzekļi sistēmiskai lietošanai - victrelis indicēts hroniska hepatīta c (chc) genotipu 1 infekcija, kombinācijā ar peginterferon alfa un ribavirīnu pieaugušiem pacientiem ar apmaksātiem aknu slimība, kuri iepriekš neapstrādātus vai kuri nav iepriekšējās terapijas ārstēšanas.

União Europeia - letão - EMA (European Medicines Agency)

sanofi winthrop industrie - klopidogrela ūdeņraža sulfāts - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - antitrombotiskie līdzekļi - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six months) or established peripheral arterial disease;adult patients suffering from acute coronary syndrome:non-st-segment-elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa);st-segment-elevation acute myocardial infarction, in combination with asa in patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic stroke (is)clopidogrel in combination with asa is indicated in:adult patients with moderate to high-risk tia (abcd2  score ≥4) or minor is (nihss  ≤3) within 24 hours of either the tia or is event. profilakse atherothrombotic un trombembolisku notikumu ātriju fibrillationin pieaugušiem pacientiem ar priekškambaru mirdzēšana, kuriem ir vismaz viena riska faktors asinsvadu notikumi, nav piemēroti apstrādei ar vitamīna k antagonisti un, kas ir zems asiņošanas risku, klopidogrelu, ir norādīts kopā ar asa novēršanas atherothrombotic un trombembolisku notikumu, tostarp insulta.

União Europeia - letão - EMA (European Medicines Agency)

janssen-cilag international nv - darunavir - hiv infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

União Europeia - letão - EMA (European Medicines Agency)

janssen-cilag international n.v. - darunavir, cobicistat - hiv infekcijas - antivirals for systemic use, antivirals for treatment of hiv infections, combinations - rezolsta ir indicēts kombinācijā ar citām pretretrovīrusu zālēm cilvēka imūndeficīta vīrusa (hiv 1) infekcijas ārstēšanai pieaugušajiem no 18 gadu vecuma. genotypic testēšana būtu ceļvedis, lietošanas rezolsta.

União Europeia - letão - EMA (European Medicines Agency)

janssen-cilag international nv - bedaquilīna fumarāts - tuberkuloze, pret multidrugiem izturīga - antimikobaktērijas - sirturo ir norādīts, izmantot atbilstošu kombināciju režīms, lai plaušu tām rezistentas tuberkulozes (mdr-tb) pieaugušo un pusaudžu pacientiem (12 gadi, lai mazāks par 18 gadiem un kas sver vismaz 30 kg), kad efektīvu ārstēšanas shēmu citādi nevar sastāv iemesli, pretestības vai panesamības. jāņem vērā oficiālās vadlīnijas par piemērotu izmantot antibakteriālas vielas.

União Europeia - letão - EMA (European Medicines Agency)

bioprojet pharma - pitolisant - narkolepsija - other nervous system drugs - wakix is indicated in adults, adolescents and children from the age of 6 years for the treatment of narcolepsy with or without cataplexy (see also section 5.

União Europeia - letão - EMA (European Medicines Agency)

janssen-cilag international nv - canagliflozin, metformīns hidrohlorīds - cukura diabēts, 2. tips - cukura diabēts - vokanamet ir norādīts pieaugušajiem vecumā no 18 gadiem un vecāki ar 2. tipa cukura diabētu, kā palīglīdzekli, lai diētu un vingrinājumiem, lai uzlabotu glycaemic kontrole:pacientiem, kas netiek pienācīgi kontrolēta to maksimāli panes devas metformīns alonein pacientiem par to maksimāli panes devas metformīns kopā ar citām glikozes samazinot zāles, tostarp insulīna, kad tie nesniedz pietiekamu kontroles glycaemic. pacientiem, kas jau tiek ārstēti ar kombināciju canagliflozin un metformīnu kā atsevišķu tabletsfor pētījuma rezultātiem attiecībā uz ogļūdeņražu terapiju, ietekmi uz glycaemic kontroles un sirds un asinsvadu notikumi, un populācijas izpēte, skatīt 4. 4, 4. 5 un 5.

União Europeia - letão - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - hydrocortisone - virsnieru nepietiekamība - kortikosteroīdi sistēmiskai lietošanai - narkotiku nepietiekamības ārstēšana pieaugušajiem.