RAMEVAL Lituania - lituaniană - SMCA (Valstybinė vaistų kontrolės tarnyba)

rameval

valentis, uab - valerijonų (valeriana off.) šaknų/sukatžolių (loenurus card.) žolės/apynių (humulus lupulus) spurgų/pipirmėčių (mentha x piperita) lapų tinktūra (1:5) - geriamieji lašai (tirpalas) - 1 ml/ml

Senebactum Lituania - lituaniană - SMCA (Valstybinė vaistų kontrolės tarnyba)

senebactum

valentis, uab - povidonas, joduotas - odos tirpalas - 100 mg/ml - povidone-iodine

TONUSSAN Lituania - lituaniană - SMCA (Valstybinė vaistų kontrolės tarnyba)

tonussan

valentis, uab - eleuterokokų (eleuterococcus senticosus) šaknų skystasis ekstraktas (1:1) - geriamieji lašai (tirpalas) - 1 ml/ml

Liugolis Lituania - lituaniană - SMCA (Valstybinė vaistų kontrolės tarnyba)

liugolis

valentis, uab - jodas - burnos gleivinės purškalas (tirpalas) - 12,5 mg/ml - antiseptics

Nityr Uniunea Europeană - lituaniană - EMA (European Medicines Agency)

nityr

cycle pharmaceuticals (europe) ltd - nitizinonas - tyrosinemijos - kiti virškinimo trakto ir metabolizmo produktus, - gydymas suaugusiųjų ir vaikų pacientams su patvirtinta diagnoze paveldimas tyrosinemia tipas 1 (ht-1) kartu su maistu, apribojimas tirozino ir fenilalanino.

PERTUSINAS Lituania - lituaniană - SMCA (Valstybinė vaistų kontrolės tarnyba)

pertusinas

valentis, uab - vaistinių čiobrelių (thymus vulgaris/zygis) žolės skystasis ekstraktas (1:2) - sirupas - 1 ml/5 ml

GINKOMED COGNI Lituania - lituaniană - SMCA (Valstybinė vaistų kontrolės tarnyba)

ginkomed cogni

valentis, uab - ginkmedžių (ginkgo biloba) lapų sausasis ekstraktas, rafinuotas ir kiekybiškai įvertintas (35-67:1) - kietosios kapsulės - 120 mg - ginkgo folium

Sitagliptin / Metformin hydrochloride Mylan Uniunea Europeană - lituaniană - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - cukrinis diabetas, 2 tipas - narkotikai, vartojami diabetu - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan 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 mylan is indicated in combination with a sulphonylurea (i. , trigubas derinys terapija), kaip papildoma priemonė kartu su dieta ir fiziniais pratimais pacientams, nepakankamai kontroliuojama, jų maksimali toleruojama dozė metforminas ir sulfonilkarbamido dariniai. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan 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.

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Uniunea Europeană - lituaniană - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - klopidogrelio besilatas - peripheral vascular diseases; stroke; myocardial infarction - antitromboziniai vaistai - secondary prevention of atherothrombotic events clopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischemic stroke (from 7 days until less than 6 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 segmento pakilimu ūmus miokardo infarktas, kartu su asr medikamentais gydytų pacientų, atitinkančių trombolizinė terapija. in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic 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. prevention of atherothrombotic and thromboembolic events in atrial fibrillation:in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. daugiau informacijos, skaitykite skyrių 5.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Uniunea Europeană - lituaniană - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - klopidogrelio hidrochloridas - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitromboziniai vaistai - , , , , secondary prevention of atherothrombotic events, , clopidogrel is indicated in: , - adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 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 medically treated patients eligible for thrombolytic therapy. , , in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic 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.  , , prevention of atherothrombotic and thromboembolic events in atrial fibrillation, in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. , , for further information please refer to section 5. , , ,.