Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

clinres farmacija d.o.o. - traneksaminska kiselina - otopina za injekciju - 100 mg/1 ml - 1 ampula otopine za injekciju od 5 ml sadrži: 500 mg traneksaminske kiseline

Europska Unija - hrvatski - EMA (European Medicines Agency)

sanofi-aventis groupe - clopidogrel, acetylsalicylic acid - acute coronary syndrome; myocardial infarction - antitrombotska sredstva - akutna koronarna infarkt syndromemyocardial .

Europska Unija - hrvatski - EMA (European Medicines Agency)

mylan ireland limited - rivaroksaban - venous thromboembolism; pulmonary embolism; acute coronary syndrome; stroke; coronary artery disease; peripheral arterial disease; atrial fibrillation - antitrombotska sredstva - rivaroxaban mylan co-administered with acetylsalicylic acid (asa) alone or with asa plus clopidogrel or ticlopidine, is indicated for the prevention of atherothrombotic events in adult patients after an acute coronary syndrome (acs) with elevated cardiac biomarkers.  rivaroxaban mylan co-administered with acetylsalicylic acid (asa), is indicated for the prevention of atherothrombotic events in adult patients with coronary artery disease (cad) or symptomatic peripheral artery disease (pad) at high risk of ischaemic events.  ------prevention of venous thromboembolism (vte) in adult patients undergoing elective hip or knee replacement surgery.  treatment of deep vein thrombosis (dvt) and pulmonary embolism (pe), and prevention of recurrent dvt and pe in adults. -------adults prevention of stroke and systemic embolism in adult   patients with non-valvular atrial fibrillation with one or more risk factors, such as congestive heart failure, hypertension, age ≥ 75 years, diabetes mellitus, prior stroke or transient ischaemic attack. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing from 30 kg to 50 kg after at least 5 days of initial parenteral anticoagulation treatment. paediatric population treatment of venous thromboembolism (vte) and prevention of vte recurrence in children and adolescents aged less than 18 years and weighing more than 50 kg after at least 5 days of initial parenteral anticoagulation treatment.

Europska Unija - hrvatski - EMA (European Medicines Agency)

gilead sciences ireland uc - bictegravir, эмтрицитабин, Тенофовир alafenamide, фумарат - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - biktarvy is indicated for the treatment of human immunodeficiency virus 1 (hiv 1) infection in adults and paediatric patients at least 2 years of age and weighing at least 14 kg i without present or past evidence of viral resistance to the integrase inhibitor class, emtricitabine or tenofovir. (vidi odjeljak 5.

Europska Unija - hrvatski - EMA (European Medicines Agency)

accord healthcare s.l.u. - ibandroninska kiselina - wounds and injuries; breast diseases; neoplastic processes; calcium metabolism disorders; water-electrolyte imbalance - lijekovi za liječenje bolesti kostiju - Ибандронатом drugačije u forprevention odrasle skeletnih događaja (patološke frakture, komplikacije kostiju, zahtijevaju radijacijske terapije ili operacije) kod bolesnika s rakom dojke i метастазами u kosti . liječenje tumor-induced гиперкальциемии sa ili bez metastaza. liječenje osteoporoze kod žena u postmenopauzi s povećanim rizikom od prijeloma (vidi odjeljak 5. smanjenje rizika od prijeloma kralježaka je pokazao učinkovitost na prijeloma vrata bedrene kosti nije instaliran.

Europska Unija - hrvatski - EMA (European Medicines Agency)

novartis vaccines and diagnostics s.r.l. - antigeni virusa influence (hemaglutinin i neuraminidaza) soja a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - cjepiva - aktivna imunizacija protiv h5n1 podtipa virusa gripe a. , , this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing a/vietnam/1194/2004 (h5n1)-like strain. , , prepandemic influenza vaccine (h5n1) novartis vaccines and diagnostic should be used in accordance with official recommendations.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

viatris hrvatska d.o.o., koranska 2, zagreb, hrvatska - nadroparinkalcij - otopina za injekciju u napunjenoj štrcaljki - 2850 iu anti-xa/0,3 ml - urbroj: 0,3 ml otopine za injekciju (1 napunjena štrcaljka) sadrži 2850 iu aktivnosti anti-xa nadroparinkalcija

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

viatris hrvatska d.o.o., koranska 2, zagreb, hrvatska - nadroparinkalcij - otopina za injekciju u napunjenoj štrcaljki - 3800 iu anti-xa/0,4 ml - urbroj: 0,4 ml otopine za injekciju (1 napunjena štrcaljka) sadrži 3800 iu aktivnosti anti-xa nadroparinkalcija

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

viatris hrvatska d.o.o., koranska 2, zagreb, hrvatska - nadroparinkalcij - otopina za injekciju u napunjenoj štrcaljki - 5700 iu anti-xa/0,6 ml - urbroj: 0,6 ml otopine za injekciju (1 napunjena štrcaljka) sadrži 5700 iu aktivnosti anti-xa nadroparinkalcija

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

viatris hrvatska d.o.o., koranska 2, zagreb, hrvatska - nadroparinkalcij - otopina za injekciju u napunjenoj štrcaljki - 7600 iu anti-xa/0,8 ml - urbroj: 0,8 ml otopine za injekciju (1 napunjena štrcaljka) sadrži 7600 iu aktivnosti anti-xa nadroparinkalcija