পর্তুগাল - পর্তুগীজ - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

medice pharma gmbh & co. kg - tirotricina + cloreto de benzalcónio + benzocaína - pastilha - 0.5 mg + 1 mg + 1.5 mg - cloreto de benzalcónio 1 mg ; benzocaína 1.5 mg ; tirotricina 0.5 mg - various - n/a - duração do tratamento: curta ou média duração

পর্তুগাল - পর্তুগীজ - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

medice pharma gmbh & co. kg - tirotricina + cloreto de benzalcónio + benzocaína - pastilha - 0.5 mg + 1 mg + 1.5 mg - cloreto de benzalcónio 1 mg ; benzocaína 1.5 mg ; tirotricina 0.5 mg - various - n/a - duração do tratamento: curta ou média duração

পর্তুগাল - পর্তুগীজ - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

chemische fabrik kreussler & co. gmbh - lauromacrogol 400 - solução injetável - 20 mg/ml - lauromacrogol 400 20 mg/ml - polidocanol - n/a - duração do tratamento: longa duração

পর্তুগাল - পর্তুগীজ - INFARMED (Autoridade Nacional do Medicamento e Produtos de Saúde)

chemische fabrik kreussler & co. gmbh - lauromacrogol 400 - solução injetável - 30 mg/ml - lauromacrogol 400 30 mg/ml - polidocanol - n/a - duração do tratamento: longa duração

ইউরোপীয় ইউনিয়ন - পর্তুগীজ - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - dalbavancin hydrochloride - soft tissue infections; skin diseases, bacterial - antibacterianos para uso sistémico, - tratamento de infecções bacterianas agudas da pele e da pele (absssi) em adultos.

ইউরোপীয় ইউনিয়ন - পর্তুগীজ - EMA (European Medicines Agency)

grünenthal gmbh - lesinurad - hiperuricemia - antigout preparações - zurampic, em combinação com um inibidor da xantina oxidase, é indicado em adultos para o tratamento adjuvante de hiperuricemia em pacientes com gota (com ou sem tophi) que não atingiram níveis de ácido úrico sérico alvo com uma dose adequada de um inibidor de xantina oxidase sozinho.

ইউরোপীয় ইউনিয়ন - পর্তুগীজ - EMA (European Medicines Agency)

grunenthal gmbh - alopurinol, lesinurad - gota - antigout preparações - duzallo é indicado em adultos para o tratamento de hyperuricaemia em gota pacientes que não tenham conseguido alvo de soro níveis de ácido úrico, com adequada dose de alopurinol sozinho.

ইউরোপীয় ইউনিয়ন - পর্তুগীজ - EMA (European Medicines Agency)

taw pharma (ireland) limited - cloridrato de clopidogrel - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - agentes antitrombóticos - , , , , 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. , , ,.

ইউরোপীয় ইউনিয়ন - পর্তুগীজ - EMA (European Medicines Agency)

sanofi winthrop industrie - clopidogrel - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - agentes antitrombóticos - prevenção secundária de aterotrombóticos eventsclopidogrel está indicado em:pacientes adultos que sofrem de infarto do miocárdio (de alguns dias até menos de 35 dias), avc isquémico (a partir de 7 dias até menos de 6 meses) ou doença arterial periférica estabelecida. pacientes adultos que sofrem de síndrome coronariana aguda:supradesnívelamento de síndrome coronariana aguda (angina instável ou não-q-onda de infarto do miocárdio), incluindo pacientes submetidos a uma colocação de stent após intervenção coronária percutânea, em combinação com ácido acetilsalicílico (asa). st segment elevation acute myocardial infarction, in combination with asa in patients undergoing percutaneous coronary intervention (including patients undergoing a stent placement) 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. prevenção de aterotrombóticos e de eventos tromboembólicos em atrial fibrillationin pacientes adultos com fibrilação atrial que tenham pelo menos um fator de risco para eventos vasculares não são adequados para o tratamento com antagonistas da vitamina k (avk) e que têm um baixo risco de sangramento, o clopidogrel é indicado em combinação com asa para a prevenção de aterotrombóticos e eventos tromboembólicos, incluindo acidente vascular cerebral.

ইউরোপীয় ইউনিয়ন - পর্তুগীজ - EMA (European Medicines Agency)

sanofi winthrop industrie - clopidogrel hidrogen sulfato - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - agentes antitrombóticos - 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. prevenção de aterotrombóticos e de eventos tromboembólicos em atrial fibrillationin pacientes adultos com fibrilação atrial que tenham pelo menos um fator de risco para eventos vasculares não são adequados para o tratamento com vitamina-k antagonistas e que têm um baixo risco de sangramento, o clopidogrel é indicado em combinação com asa para a prevenção de aterotrombóticos e eventos tromboembólicos, incluindo acidente vascular cerebral.