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

haleon czech republic s.r.o., Česká republika - uhličitan vápenatý a cholekalciferol - 39 - soli a ionty pro p.o. a parent. aplikÁciu

Európska únia - slovenčina - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - atogepant - poruchy migrény - aquipta is indicated for prophylaxis of migraine in adults who have at least 4 migraine days per month.

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

haleon czech republic s.r.o., Česká republika - kyselina acetylsalicylová, kombinácie s výnimkou psycholeptík - 07 - analgetica, antipyretica

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

gedeon richter plc., maďarsko - levonorgestrel - 17 - anticoncipientia

Európska únia - slovenčina - EMA (European Medicines Agency)

novartis europharm limited - erenumab - poruchy migrény - analgetiká - aimovig je indikovaný na profylaxiu migrény u dospelých, ktorí majú aspoň 4 migréna dní za mesiac pri začatí liečby s aimovig.

Európska únia - slovenčina - EMA (European Medicines Agency)

eli lilly nederland b.v. - galcanezumab - poruchy migrény - analgesics, galcanezumab - emgality je indikovaný na profylaxiu migrény u dospelých, ktorí majú aspoň 4 migréna dní za mesiac.

Európska únia - slovenčina - EMA (European Medicines Agency)

eli lilly nederland b.v. - lasmiditan succinate - poruchy migrény - analgetiká - rayvow is indicated for the acute treatment of the headache phase of migraine attacks, with or without aura in adults.

Európska únia - slovenčina - EMA (European Medicines Agency)

teva pharma b.v.  - lamivudine, zidovudine - hiv infekcie - antivirotiká na systémové použitie - lamivudin / zidovudine teva je indikovaný v kombinovanej antiretrovírusovej liečbe na liečbu infekcie vírusom ľudskej imunodeficiencie (hiv).

Európska únia - slovenčina - EMA (European Medicines Agency)

teva gmbh - fremanezumab - poruchy migrény - calcitonin gene-related peptide (cgrp) antagonists - ajovy je indikovaný na profylaxiu migrény u dospelých, ktorí majú aspoň 4 migréna dní za mesiac.

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.