Estonja - Estonjan - Ravimiamet

pharmaswiss ceska republika s.r.o. - esetimiib - tablett - 10mg 10tk; 10mg 28tk; 10mg 20tk; 10mg 84tk; 10mg 50tk; 10mg 30tk; 10mg 300tk; 10mg 90tk; 10mg 98tk

Estonja - Estonjan - Ravimiamet

pharma nord aps - melatoniin - õhukese polümeerikattega tablett - 3mg 30tk

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

mundipharma corporation (ireland) limited - pegfilgrastim - neutropeenia - immunostimulants, - vähendada kestus neutropenia ja esinemissagedus febriilsed neutropenia tõttu keemiaravi.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

viatris limited - klopidogreel-besilaat - peripheral vascular diseases; stroke; myocardial infarction - antitrombootilised ained - 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 segmendi elevatsiooniga ägeda müokardi infarkti korral kombinatsioonis asa on meditsiiniliselt ravitud patsientide abikõlblikud trombolüütiline ravi. 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. täiendava teabe jaoks vt osa 5.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

glaxosmithkline (ireland) limited - belimumab - erütematoosne luupus, süsteemne - immunosupressandid - benlysta on näidustatud add-ravi patsientidel vanuses 5 aastat ja vanemad, aktiivne, autoantibody positiivne süsteemne erütematoosne luupus (sle) suure tõenäosusega haiguse tegevus (e. positiivseid anti dsdna ja väike täiendus) vaatamata standardi ravi. benlysta is indicated in combination with background immunosuppressive therapies for the treatment of adult patients with active lupus nephritis.

Unjoni Ewropea - Estonjan - EMA (European Medicines Agency)

mylan s.a.s. - pregabaliin - anxiety disorders; neuralgia; epilepsy - antiepileptics, - epilepsypregabalin mylan pharma on näidustatud adjunctive ravi täiskasvanutel, osaline krambid koos või ilma sekundaarse üldistada. generaliseerunud Ärevus disorderpregabalin mylan pharma on näidustatud ravi generaliseerunud Ärevushäire (gad) täiskasvanutel.

Estonja - Estonjan - Ravimiamet

venus pharma gmbh - tsefuroksiim - süste-/infusioonilahuse pulber - 750mg 1tk

Estonja - Estonjan - Ravimiamet

venus pharma gmbh - tsefuroksiim - süste-/infusioonilahuse pulber - 1,5g 1tk

Estonja - Estonjan - Ravimiamet

venus pharma gmbh - tseftriaksoon - süste-/infusioonilahuse pulber - 2g 10tk; 2g 1tk; 2g 5tk

Estonja - Estonjan - Ravimiamet

venus pharma gmbh - tseftriaksoon - süste-/infusioonilahuse pulber - 1g 1tk; 1g 10tk