Evropska unija - slovenščina - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a.  - respiratory syncytial virus recombinant glycoprotein f stabilised in the pre-fusion conformation (rsvpref3) produced in chinese hamster ovary (cho) cells by recombinant dna technology - infekcije respiratornih sincicijskih virusov - cepiva - arexvy is indicated for active immunisation for the prevention of lower respiratory tract disease (lrtd) caused by respiratory syncytial virus in adults 60 years of age and older. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Evropska unija - slovenščina - 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 - gripa, človek - cepiva - supemtek is indicated for active immunization for the prevention of influenza disease in adults. supemtek should be used in accordance with official recommendations.

Evropska unija - slovenščina - EMA (European Medicines Agency)

sun pharmaceutical industries (europe) b.v. - ertapenem natrij - bakterijske okužbe - ertapenem - treatmentertapenem sun is indicated in paediatric patients (3 months to 17 years of age) and in adults for the treatment of the following infections when caused by bacteria known or very likely to be susceptible to ertapenem and when parenteral therapy is required (see sections 4. 4 in 5. 1):- intra-abdominal infections- community acquired pneumonia- acute gynaecological infections- diabetic foot infections of the skin and soft tissue (see section 4. 4)preventionertapenem sun is indicated in adults for the prophylaxis of surgical site infection following elective colorectal surgery (see section 4. upoštevati je treba uradne smernice za ustrezno uporabo protibakterijsko agenti.

Evropska unija - slovenščina - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - teriparatid - osteoporosis; osteoporosis, postmenopausal - kalcij homeostaza - teriparatide sun is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Evropska unija - slovenščina - EMA (European Medicines Agency)

novo nordisk a/s - nonacog beta pegol - hemofilija b - antihemoragije - zdravljenje in profilaksa krvavitve pri bolnikih s hemofilijo b (prirojene pomanjkljivosti faktorja ix). , refixia can be used for all age groups.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - roflumilast - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - daliresp je indicirano za vzdrževalno zdravljenje hude kronična obstruktivna pljučna bolezen (kopb) (fev1 po bronchodilator manj kot 50 % napovedati) povezane z kronični bronhitis pri odraslih bolnikih z zgodovino pogoste poslabšanj kot dodatek bronchodilator zdravljenje.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - roflumilast - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - daxas je indicirano za vzdrževalno zdravljenje hude kronična obstruktivna pljučna bolezen (kopb) (fev1 po bronchodilator manj kot 50 % napovedati) povezane z kronični bronhitis pri odraslih bolnikih z zgodovino pogoste poslabšanj kot dodatek za bronchodilator zdravljenje.

Evropska unija - slovenščina - EMA (European Medicines Agency)

astrazeneca ab - roflumilast - pljučna bolezen, kronična obstruktivna bolezen - zdravila za obstruktivne pljučne bolezni, - libertek je indicirano za vzdrževalno zdravljenje hude kronična obstruktivna pljučna bolezen (kopb) (fev1 po bronchodilator manj kot 50 % napovedati) povezane z kronični bronhitis pri odraslih bolnikih z zgodovino pogoste poslabšanj kot dodatek bronchodilator zdravljenje.

Evropska unija - slovenščina - EMA (European Medicines Agency)

teva b.v. - lipegfilgrastim - nevtropenija - immunostimulants, , colony stimulating factors - lonquex is indicated in adults and in children 2 years of age and older for reduction in the duration of neutropenia and the incidence of febrile neutropenia in patients treated with cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes).

Evropska unija - slovenščina - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - lanadelumab - angioedem, dedno - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.