체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 11237 levetiracetam - potahovaná tableta - 500mg - levetiracetam

유럽 연합 - 체코어 - EMA (European Medicines Agency)

krka, d.d., novo mesto - desloratadin - rhinitis, allergic, perennial; rhinitis, allergic, seasonal; urticaria - antihistaminika pro systémové použití, - přípravek dasselta je indikován k zmírnění příznaků spojených s:alergickou rýmou;kopřivka.

체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 2418 metformin-hydrochlorid - potahovaná tableta - 1000mg - metformin

체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 2418 metformin-hydrochlorid - potahovaná tableta - 500mg - metformin

체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 2418 metformin-hydrochlorid - potahovaná tableta - 850mg - metformin

체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 2418 metformin-hydrochlorid - tableta s prodlouženým uvolňováním - 1000mg - metformin

체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 2418 metformin-hydrochlorid - tableta s prodlouženým uvolňováním - 500mg - metformin

체코 - 체코어 - SUKL (Státní ústav pro kontrolu léčiv)

stada arzneimittel ag, bad vilbel array - 2418 metformin-hydrochlorid - tableta s prodlouženým uvolňováním - 750mg - metformin

유럽 연합 - 체코어 - EMA (European Medicines Agency)

eli lilly nederland b.v. - tadalafil - hypertenze, plicní - urologika - adultstreatment of pulmonary arterial hypertension (pah) classified as who functional class ii and iii, to improve exercise capacity (see section 5. Účinnost byla prokázána u idiopatické pah (ipah) a u pah souvisejících s vaskulárním onemocněním kolagenu. paediatric populationtreatment of paediatric patients aged 2 years and above with pulmonary arterial hypertension (pah) classified as who functional class ii and iii.

유럽 연합 - 체코어 - EMA (European Medicines Agency)

taw pharma (ireland) limited - hydrochlorid klopidogrelu - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitrombotické činidla - , , , , 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. , , ,.