Łotwa - łotewski - Zāļu valsts aģentūra

glaxosmithkline biologicals s.a., belgium - gripas vakcīna (šķelts virions, inaktivēts) - suspensija injekcijām pilnšļircē - 0,5 ml

Łotwa - łotewski - Zāļu valsts aģentūra

mylan ire healthcare ltd, ireland - gripas vakcīna (virsmas antigēns, inaktivēta) - suspensija injekcijām pilnšļircē

Łotwa - łotewski - Zāļu valsts aģentūra

glaxosmithkline biologicals s.a., belgium - difterijas, stingumkrampju, acelulāra garā klepus un poliomielīta (inaktivēta) vakcīna (adsorbēta) - suspensija injekcijām pilnšļircē

Łotwa - łotewski - Zāļu valsts aģentūra

sanofi pasteur, france - gripas vakcīna (šķelts virions, inaktivēts) - suspensija injekcijām pilnšļircē - 0,5 ml

Unia Europejska - łotewski - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - other antineoplastic agents - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

Łotwa - łotewski - Zāļu valsts aģentūra

viatris healthcare limited, ireland - gripas vakcīna (virsmas antigēns, inaktivēta) - suspensija injekcijām pilnšļircē

Łotwa - łotewski - Zāļu valsts aģentūra

sanofi pasteur, france - gripas vakcīna (šķelts virions, inaktivēts) - suspensija injekcijām pilnšļircē - 0,7 ml

Unia Europejska - łotewski - EMA (European Medicines Agency)

sanofi pasteur - influenza a virus subtype h1n1 haemagglutinin, recombinant, influenza a virus subtype h3n2 haemagglutinin, recombinant, influenza b virus victoria lineage haemagglutinin, recombinant, influenza b virus yamagata lineage haemagglutinin, recombinant - gripas, cilvēka - vakcīnas - supemtek is indicated for active immunization for the prevention of influenza disease in adults. supemtek should be used in accordance with official recommendations.

Unia Europejska - łotewski - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - maribavir - citomegalovīrusu infekcijas - pretvīrusu līdzekļi sistēmiskai lietošanai - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). jāņem vērā oficiālās vadlīnijas par piemērotu izmantot pretvīrusu aģentu.

Unia Europejska - łotewski - EMA (European Medicines Agency)

acino ag - clopidogrel - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antitrombotiskie līdzekļi - clopidogrel is indicated in adults for the prevention of atherothrombotic events in: , , , 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, 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, patients suffering from acute coronary syndrome. , ,.