Xenleta Unia Europejska - chorwacki - EMA (European Medicines Agency)

xenleta

nabriva therapeutics ireland dac - lefamulin acetate - pneumonia, bacterial; community-acquired infections - antibakterijski lijekovi za sistemsku primjenu, - xenleta is indicated for the treatment of community-acquired pneumonia (cap) in adults when it is considered inappropriate to use antibacterial agents that are commonly recommended for the initial treatment of cap or when these have failed. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Comirnaty Unia Europejska - chorwacki - EMA (European Medicines Agency)

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - cjepiva - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. korištenje ovog cjepiva mora se provoditi u skladu sa službenim preporukama.

Vaxzevria (previously COVID-19 Vaccine AstraZeneca) Unia Europejska - chorwacki - EMA (European Medicines Agency)

vaxzevria (previously covid-19 vaccine astrazeneca)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - cjepiva - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. korištenje ovog cjepiva mora se provoditi u skladu sa službenim preporukama.

NexGard Combo Unia Europejska - chorwacki - EMA (European Medicines Agency)

nexgard combo

boehringer ingelheim vetmedica gmbh - eprinomectin, esafoxolaner, praziquantel - eprinomectin, combinations, , avermectins, antiparasitic products, insecticides and repellents - mačke - for cats with, or at risk from mixed infections by cestodes, nematodes and ectoparasites. veterinarski medicinski proizvod je isključivo ukazuje na to kada se sve tri grupe su usmjereni u isto vrijeme.

Klisyri Unia Europejska - chorwacki - EMA (European Medicines Agency)

klisyri

almirall, s.a. - tirbanibulin - keratosis, actinić - antibiotici i kemoterapeutici za dermatološku uporabu - klisyri is indicated for the field treatment of non-hyperkeratotic, non-hypertrophic actinic keratosis (olsen grade 1) of the face or scalp in adults.

Abecma Unia Europejska - chorwacki - EMA (European Medicines Agency)

abecma

bristol-myers squibb pharma eeig - idecabtagene vicleucel - multiple myeloma; neoplasms; cancer; neoplasms, plasma cell; hemostatic disorders; vascular diseases; cardiovascular diseases; paraproteinemias; blood protein disorders; hematologic diseases; hemic and lymphatic diseases; hemorrhagic disorders; infectious mononucleosis; lymphoproliferative disorders; immunoproliferative disorders; immune system diseases - antineoplastična sredstva - abecma 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.

Ozawade Unia Europejska - chorwacki - EMA (European Medicines Agency)

ozawade

bioprojet pharma - pitolisant - sleep apnea, obstructive - ostali lijekovi protiv živčanog sustava - ozawade is indicated to improve wakefulness and reduce excessive daytime sleepiness (eds) in adult patients with obstructive sleep apnoea (osa).

Bronchostop Trio oralna otopina Chorwacja - chorwacki - HALMED (Agencija za lijekove i medicinske proizvode)

bronchostop trio oralna otopina

kwizda pharma gmbh, effingergasse 21, beč, austrija - suhi ekstrakt korijena običnog bijelog sljeza (7-9:1), ekstrakcijsko otapalo: voda suhi ekstrakt lipovog cvijeta (3-8:1), ekstrakcijsko otapalo: voda suhi ekstrakt trpučevog lista (4-6:1), ekstrakcijsko otapalo: voda - oralna otopina - urbroj: 15 ml (= 16,3 g) oralne otopine sadrži: 187,5 mg ekstrakta (kao suhi ekstrakt) iz althaea officinalis l., radix (korijen bijelog sljeza) (7-9:1), ekstrakcijsko otapalo: voda. 136,4 mg ekstrakta (kao suhi ekstrakt) tilia cordata miller, tilia platyphyllos scop., tilia x vulgaris heyne ili njihove mješavine, flos (lipov cvijet) (3-8:1), ekstrakcijsko otapalo: voda. 150,0 mg ekstrakta (kao suhi ekstrakt) iz plantago lanceolata l., folium (trpučev list) (4-6:1),ekstrakcijsko otapalo: voda.

Tavneos Unia Europejska - chorwacki - EMA (European Medicines Agency)

tavneos

vifor fresenius medical care renal pharma france - avacopan - microscopic polyangiitis; wegener granulomatosis - imunosupresivi - tavneos, in combination with a rituximab or cyclophosphamide regimen, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (gpa) or microscopic polyangiitis (mpa).

Artesunate Amivas Unia Europejska - chorwacki - EMA (European Medicines Agency)

artesunate amivas

amivas ireland ltd - artesunate - malarija - antiprotozoals - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje противомалярийных posrednika.