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

prezista

janssen-cilag international nv - danmavir - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adult and paediatric patients from the age of 3 years and at least 15 kg body weight. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). in deciding to initiate treatment with prezista co administered with cobicistat or low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista 75 mg, 150 mg, and 600 mg tablets may be used to provide suitable dose regimens:for the treatment of hiv 1 infection in antiretroviral treatment (art) experienced adult patients, including those that have been highly pre treated. for the treatment of hiv 1 infection in paediatric patients from the age of 3 years and at least 15 kg body weight. in deciding to initiate treatment with prezista co administered with low dose ritonavir, careful consideration should be given to the treatment history of the individual patient and the patterns of mutations associated with different agents. genotypic or phenotypic testing (when available) and treatment history should guide the use of prezista. prezista, co administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv 1) infection. prezista, co administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv 1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg). prezista 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv 1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are:antiretroviral therapy (art) naïve. art experienced with no darunavir resistance associated mutations (drv rams) and who have plasma hiv 1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 106/l. in deciding to initiate treatment with prezista in such art experienced patients, genotypic testing should guide the use of prezista.

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

telzir

viiv healthcare bv - fosamprenavir kalcij - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - telzir u kombinaciji s niske doze ritonavira je indiciran za liječenje human-immunodeficiency-virus-type-1-infected odraslih, adolescenata i djece u dobi od šest godina i više u kombinaciji s drugim bosentana i antiretrovirusnih lijekova. u umjereno arv-iskusni odrasli, Телзир u kombinaciji s niskom dozom ritonavir nije bilo prikazano, da bude jednako učinkovit kao i лопинавир / ritonavir. komparativna istraživanja su provedena u djece i adolescenata. u velikoj mjeri prethodno tretiranih pacijenata, korištenje Телзир u kombinaciji s niskom dozom ritonavir je još uvijek nedovoljno istražena. u протеаза-inhibitor-iskusan pacijenata, izbor Телзир mora se temeljiti na individualnoj virusne rezistencije ispitivanje i povijesti liječenje .

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

prevymis

merck sharp & dohme b.v. - letermovir - infekcije citomegalovirusa - antivirusni lijekovi za sustavnu uporabu - prevymis je indiciran za profilaksu citomegalovirus (cmv) reaktivacije i bolesti u odraslih cmv seropozitivne primatelja [r +] transplantacija alogenih krvotvornih matičnih stanica (hsct). treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antivirusnih lijekova.

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

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - dijabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Articel-Am 10 mg/10 mg tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

articel-am 10 mg/10 mg tablete

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - perindopriltosilat amlodipinbesilat - tableta - 10 mg + 10 mg - urbroj: jedna tableta sadrži 10 mg perindopriltosilata što odgovara 6,8 mg perindoprila i 13,87 mg amlodipinbesilata što odgovara 10 mg amlodipina

Articel-Am 10 mg/5 mg tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

articel-am 10 mg/5 mg tablete

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - perindopriltosilat amlodipinbesilat - tableta - 10 mg + 5 mg - urbroj: jedna tableta sadrži 10 mg perindopriltosilata što odgovara 6,8 mg perindoprila i 6,935 mg amlodipinbesilata što odgovara 5 mg amlodipina

Articel-Am 5 mg/10 mg tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

articel-am 5 mg/10 mg tablete

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - perindopriltosilat amlodipinbesilat - tableta - 5 mg + 10 mg - urbroj: jedna tableta sadrži 5 mg perindopriltosilata što odgovara 3,4 mg perindoprila i 13,87 mg amlodipinbesilata što odgovara 10 mg amlodipina

Articel-Am 5 mg/5 mg tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

articel-am 5 mg/5 mg tablete

pliva hrvatska d.o.o., prilaz baruna filipovića 25, zagreb, hrvatska - perindopriltosilat amlodipinbesilat - tableta - 5 mg + 5 mg - urbroj: jedna tableta sadrži 5 mg perindopriltosilata što odgovara 3,4 mg perindoprila i 6,935 mg amlodipinbesilata što odgovara 5 mg amlodipina

Lopinavir/Ritonavir Sandoz 200 mg/50 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

lopinavir/ritonavir sandoz 200 mg/50 mg filmom obložene tablete

sandoz d.o.o., maksimirska 120, zagreb - lopinavirum, ritonavirum - filmom obložena tableta - 200 mg + 50 mg - urbroj: svaka filmom obložena tableta sadrži 200 mg lopinavira i 50 mg ritonavira

Natrixam 1,5 mg/10 mg tablete s prilagođenim oslobađanjem Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

natrixam 1,5 mg/10 mg tablete s prilagođenim oslobađanjem

servier pharma d.o.o., tuškanova 37, zagreb, hrvatska - indapamid amlodipinbesilat - tableta s prilagođenim oslobađanjem - 1,5 mg + 10 mg - urbroj: jedna tableta sadrži 1,5 mg indapamida i 13,87 mg amlodipinbesilata što odgovara 10 mg amlodipina