Aciclovir Accord 25 mg/ml Koncentrat do sporządzania roztworu do infuzji Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

aciclovir accord 25 mg/ml koncentrat do sporządzania roztworu do infuzji

accord healthcare polska sp. z o.o. - aciclovirum - koncentrat do sporządzania roztworu do infuzji - 25 mg/ml

Maxiseptic (1 mg + 20 mg)/ml Aerozol na skórę, roztwór Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

maxiseptic (1 mg + 20 mg)/ml aerozol na skórę, roztwór

bausch health ireland ltd. - octenidini dihydrochloridum + phenoxyethanol - aerozol na skórę, roztwór - (1 mg + 20 mg)/ml

Maxiseptic (1 mg + 20 mg)/ml Roztwór na skórę Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

maxiseptic (1 mg + 20 mg)/ml roztwór na skórę

bausch health ireland limited - octenidini dihydrochloridum + phenoxyethanolum - roztwór na skórę - (1 mg + 20 mg)/ml

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Unia Europejska - polski - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - chlorowodorek klopidogrelu - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - Środki przeciwzakrzepowe - , , , , 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. , , ,.

Neurobion Advance 100 mg + 50 mg + 1 mg Tabletki powlekane Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

neurobion advance 100 mg + 50 mg + 1 mg tabletki powlekane

p&g health germany gmbh - thiamini nitras + pyridoxini hydrochloridum + cyanocobalaminum - tabletki powlekane - 100 mg + 50 mg + 1 mg

Clopidogrel Viatris (previously Clopidogrel Taw Pharma) Unia Europejska - polski - EMA (European Medicines Agency)

clopidogrel viatris (previously clopidogrel taw pharma)

viatris limited - besylan klopidogrelu - peripheral vascular diseases; stroke; myocardial infarction - Środki przeciwzakrzepowe - 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). elewacja segmentu st ostry zawał mięśnia sercowego, w połączeniu z asa w leczenie pacjentów kwalifikujących się do leczenia trombolitycznego. 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. aby uzyskać więcej informacji, proszę odnieść się do rozdziału 5.

Kalydeco Unia Europejska - polski - EMA (European Medicines Agency)

kalydeco

vertex pharmaceuticals (ireland) limited - iwakaftor - zwłóknienie torbielowate - inne produkty układu oddechowego - kalydeco tablets are indicated:as monotherapy for the treatment of adults, adolescents, and children aged 6 years and older and weighing 25 kg or more with cystic fibrosis (cf) who have an r117h cftr mutation or one of the following gating (class iii) mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene: g551d, g1244e, g1349d, g178r, g551s, s1251n, s1255p, s549n or s549r (see sections 4. 4 i 5. in a combination regimen with tezacaftor/ivacaftor tablets for the treatment of adults, adolescents, and children aged 6 years and older with cystic fibrosis (cf) who are homozygous for the f508del mutation or who are heterozygous for the f508del mutation and have one of the following mutations in the cftr gene: p67l, r117c, l206w, r352q, a455e, d579g, 711+3a→g, s945l, s977f, r1070w, d1152h, 2789+5g→a, 3272 26a→g, and 3849+10kbc→t. in a combination regimen with ivacaftor/tezacaftor/elexacaftor tablets for the treatment of adults, adolescents, and children aged 6 years and older with cystic fibrosis (cf) who have at least one f508del mutation in the cftr gene (see section 5. kalydeco granules are indicated for the treatment of infants aged at least 4 months, toddlers and children weighing 5 kg to less than 25 kg with cystic fibrosis (cf) who have an r117h cftr mutation or one of the following gating (class iii) mutations in the cftr gene: g551d, g1244e, g1349d, g178r, g551s, s1251n, s1255p, s549n or s549r (see sections 4. 4 i 5. in a combination regimen with ivacaftor/tezacaftor/elexacaftor for the treatment of cystic fibrosis (cf) in paediatric patients aged 2 to less than 6 years who have at least one f508del mutation in the cftr gene.

Brinzolamide Accord 10 mg/ml Krople do oczu, zawiesina Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

brinzolamide accord 10 mg/ml krople do oczu, zawiesina

accord healthcare polska sp. z o.o. - brinzolamidum - krople do oczu, zawiesina - 10 mg/ml

Mantreda 15 mg Tabletki powlekane Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

mantreda 15 mg tabletki powlekane

sigillata limited - rivaroxabanum - tabletki powlekane - 15 mg

Mantreda 20 mg Tabletki powlekane Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

mantreda 20 mg tabletki powlekane

sigillata limited - rivaroxabanum - tabletki powlekane - 20 mg