Senstend Europska Unija - hrvatski - EMA (European Medicines Agency)

senstend

plethora pharma solutions limited - lidokain, prilocaine - prerane ejakulacije - anestetici - senstend indiciran za liječenje primarne prerane ejakulacije kod odraslih muškaraca.

Xospata Europska Unija - hrvatski - EMA (European Medicines Agency)

xospata

astellas pharma europe b.v. - gilteritinib фумарат - leukemija, mieloidna, akutna - antineoplastična sredstva - xospata prikazan kao monoterapija za liječenje odraslih pacijenata s relaps ili vatrostalne akutne mijeloične leukemije (aml) s перегласовкой flt3 na .

Veklury Europska Unija - hrvatski - EMA (European Medicines Agency)

veklury

gilead sciences ireland uc - remdesivir - covid-19 virus infection - veklury is indicated for the treatment of coronavirus disease 2019 (covid 19) in:adults and paediatric patients (at least 4 weeks of age and weighing at least 3 kg) with pneumonia requiring supplemental oxygen (low- or high-flow oxygen or other non-invasive ventilation at start of treatment)adults and paediatric patients (weighing at least 40 kg) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

Byfavo Europska Unija - hrvatski - EMA (European Medicines Agency)

byfavo

paion deutschland gmbh - remimazolam besilate - svjesna sedacija - psycholeptics - remimazolam is indicated in adults for procedural sedation. remimazolam 50 mg is indicated in adults for intravenous induction and maintenance of general anaesthesia.

Vazkepa Europska Unija - hrvatski - EMA (European Medicines Agency)

vazkepa

amarin pharmaceuticals ireland limited - icosapent ethyl - dislipidemije - sredstva za modifikaciju lipida - indicated to reduce cardiovascular risk as an adjunct to statin therapy.

BroPair Spiromax Europska Unija - hrvatski - EMA (European Medicines Agency)

bropair spiromax

teva b.v. - xinafoate сальметерол, flutikazon propionat - astma - lijekovi za opstruktivne plućne bolesti dišnih putova, - bropair spiromax is indicated in the regular treatment of asthma in adults and adolescents aged 12 years and older not adequately controlled with inhaled corticosteroids and ‘as needed’ inhaled short-acting β₂ agonists.

Seffalair Spiromax Europska Unija - hrvatski - EMA (European Medicines Agency)

seffalair spiromax

teva b.v. - fluticasone propionate, salmeterol xinafoate - astma - lijekovi za opstruktivne plućne bolesti dišnih putova, - seffalair spiromax is indicated in the regular treatment of asthma in adults and adolescents aged 12 years and older not adequately controlled with inhaled corticosteroids and ‘as needed’ inhaled short-acting β₂ agonists.

Evkeeza Europska Unija - hrvatski - EMA (European Medicines Agency)

evkeeza

ultragenyx germany gmbh - evinacumab - hiperkolesterolemija - sredstva za modifikaciju lipida - evkeeza is indicated as an adjunct to diet and other low-density lipoprotein-cholesterol (ldl-c) lowering therapies for the treatment of adult and adolescent patients aged 12 years and older with homozygous familial hypercholesterolaemia (hofh).

Carvykti Europska Unija - hrvatski - EMA (European Medicines Agency)

carvykti

janssen-cilag international nv - ciltacabtagene autoleucel - multipli mijelom - carvykti is indicated for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Emtriva Europska Unija - hrvatski - EMA (European Medicines Agency)

emtriva

gilead sciences ireland uc - emtricitabina - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - emtriva je indicirana za liječenje hiv-1 inficiranih odraslih i djece u kombinaciji s drugim antiretrovirusnim sredstvima. ovaj prikaz se temelji na istraživanjima u liječenju naivnih bolesnika i liječenje bolesnika sa stalnim вирусологическим kontrolom. nema iskustvo korištenja Эмтрива kod pacijenata koji nisu u mogućnosti da ih trenutnog načina rada ili пропустившие nekoliko krugova. pri odabiru novog profila za pacijente koji nisu антиретровирусные lijekovi, pažljivo razmatranje treba dati model mutacije povezane s različitim lijekovima i povijest liječenja pojedinog pacijenta. gdje je to moguće, ispitivanje otpora može biti prikladno.