Európska únia - slovenčina - EMA (European Medicines Agency)

pfizer europe ma eeig - pemetrexed disodium, pemetrexed disodium hemipentahydrate - carcinoma, non-small-cell lung; mesothelioma - antineoplastické činidlá - malignant pleural mesotheliomapemetrexed pfizer in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancerpemetrexed pfizer in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. pemetrexed pfizer is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. pemetrexed pfizer is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Európska únia - slovenčina - EMA (European Medicines Agency)

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 - vakcíny - 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. použitie tejto vakcíny by mali byť v súlade s oficiálne odporúčania.

Európska únia - slovenčina - EMA (European Medicines Agency)

pfizer europe ma eeig - pemetrexed ditromethamine - carcinoma, non-small-cell lung; mesothelioma - kyseliny listovej analógy, antimetabolites - malígny pleurálna mesotheliomapemetrexed hospira uk limited v kombinácii s cisplatin je indikovaný na liečbu chemoterapiou insitného pacientov s unresectable malígny pleurálna mesothelioma. non-small cell lung cancerpemetrexed hospira uk limited v kombinácii s cisplatin je uvedené, za prvé-line liečbu pacientov s lokálne pokročilým alebo metastatickým non-small cell lung cancer iné ako prevažne dlaždicových buniek histology (pozri smpc oddiel 5. pemetrexed hospira uk limited je označené ako monotherapy pre udržiavaciu liečbu lokálne pokročilým alebo metastatickým non-small cell lung cancer iné ako prevažne dlaždicových buniek histology u pacientov, ktorých ochorenie nie postupoval bezprostredne po platinum-založené chemoterapia (pozri smpc oddiel 5. pemetrexed hospira uk limited je označené ako monotherapy pre druhý riadok liečbu pacientov s lokálne pokročilým alebo metastatickým non-small cell lung cancer iné ako prevažne dlaždicových buniek histology (pozri smpc oddiel 5.

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - klindamycín - 15 - antibiotica (proti mikrob. a vÍrusovÝm infekciam)

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - očkovacia látka proti meningokom c, purifikovaný polysacharidový konjugovaný antigén - 59 - immunopraeparata

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - klindamycín - 15 - antibiotica (proti mikrob. a vÍrusovÝm infekciam)

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - očkovacia látka proti kliešťovej encefalitíde, inaktivovaná, neporušený vírus - 59 - immunopraeparata

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - dinoprostón - 54 - gynaecologica

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - karboprost - 81 - uterotonica

Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pfizer europe ma eeig, belgicko - očkovacia látka proti kliešťovej encefalitíde, inaktivovaná, neporušený vírus - 59 - immunopraeparata