Comirnaty Evropská unie - slovinština - 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 - cepiva - 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. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Xofluza Evropská unie - slovinština - EMA (European Medicines Agency)

xofluza

roche registration gmbh - baloxavir marboxil - gripa, človek - antivirusi za sistemsko uporabo - treatment of influenzaxofluza is indicated for the treatment of uncomplicated influenza in patients aged 1 year and above. post exposure prophylaxis of influenzaxofluza is indicated for post-exposure prophylaxis of influenza in individuals aged 1 year and above. xofluza should be used in accordance with official recommendations.

Jcovden (previously COVID-19 Vaccine Janssen) Evropská unie - slovinština - EMA (European Medicines Agency)

jcovden (previously covid-19 vaccine janssen)

janssen-cilag international nv - adenovirus type 26 encoding the sars-cov-2 spike glycoprotein (ad26.cov2-s) - covid-19 virus infection - cepiva - jcovden is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 years of age and older. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Copiktra Evropská unie - slovinština - EMA (European Medicines Agency)

copiktra

secura bio limited - duvelisib - leukemia, lymphocytic, chronic, b-cell; lymphoma, follicular - antineoplastična sredstva - copiktra monotherapy is indicated for the treatment of adult patients with: relapsed or refractory chronic lymphocytic leukaemia (cll) after at least two prior therapies.  follicular lymphoma (fl) that is refractory to at least two prior  systemic therapies.

Vaxzevria (previously COVID-19 Vaccine AstraZeneca) Evropská unie - slovinština - EMA (European Medicines Agency)

vaxzevria (previously covid-19 vaccine astrazeneca)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - cepiva - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. uporaba tega cepiva mora biti v skladu z uradnimi priporočili.

Influvac Tetra suspenzija za injiciranje v napolnjeni injekcijski brizgi Slovinsko - slovinština - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

influvac tetra suspenzija za injiciranje v napolnjeni injekcijski brizgi

ha seva b/phuket/3073/2013, divji tip, podoben sevu b/phuket/3073/2013; ha seva b/washington/02/2019, divji tip, podoben sevu b/washington/02/2019; ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p; ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e0826 - suspenzija za injiciranje v napolnjeni injekcijski brizgi - ha seva b/phuket/3073/2013, divji tip, podoben sevu b/phuket/3073/2013 15 µg / 1 brizga  ha seva b/washington/02/2019, divji tip, podoben sevu b/washington/02/201915 µg / 1 brizga  ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p15 µg / 1 brizga  ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e082615 µg / 1 brizga; ha seva b/washington/02/2019, divji tip, podoben sevu b/washington/02/2019 15 µg / 1 brizga  ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p15 µg / 1 brizga  ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e082615 µg / 1 brizga; ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p 15 µg / 1 brizga  ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e082615 µg / 1 brizga; ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e0826 - cepivo proti gripi, z delci virusov ali s površinskimi antigeni, inaktivirano

Influvac Tetra suspenzija za injiciranje v napolnjeni injekcijski brizgi Slovinsko - slovinština - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

influvac tetra suspenzija za injiciranje v napolnjeni injekcijski brizgi

ha seva b/phuket/3073/2013, divji tip, podoben sevu b/phuket/3073/2013; ha seva b/washington/02/2019, divji tip, podoben sevu b/washington/02/2019; ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p; ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e0826 - suspenzija za injiciranje v napolnjeni injekcijski brizgi - ha seva b/phuket/3073/2013, divji tip, podoben sevu b/phuket/3073/2013 15 µg / 1 brizga  ha seva b/washington/02/2019, divji tip, podoben sevu b/washington/02/201915 µg / 1 brizga  ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p15 µg / 1 brizga  ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e082615 µg / 1 brizga; ha seva b/washington/02/2019, divji tip, podoben sevu b/washington/02/2019 15 µg / 1 brizga  ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p15 µg / 1 brizga  ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e082615 µg / 1 brizga; ha seva a/victoria/2570/2019, ivr-215, podoben sevu a/victoria/2570/2019 (h1n1)p 15 µg / 1 brizga  ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e082615 µg / 1 brizga; ha seva ivr-224 (iz seva a/cambodia/e0826360/2020, podoben sevu a/cambodia/e0826 - cepivo proti gripi, z delci virusov ali s površinskimi antigeni, inaktivirano