Dukoral Európska únia - slovenčina - EMA (European Medicines Agency)

dukoral

valneva sweden ab - rekombinantnej cholery toxínu b podjednotky, vibrio cholerae 01 - cholera; immunization - vakcíny - dukoral je indikovaný na aktívnu imunizáciu proti chorobám spôsobeným vibrio cholerae séroskupinou o1 u dospelých a detí vo veku od 2 rokov, ktorí navštevujú endemické / epidemické oblasti. použitie dukoral by mali byť stanovené na základe oficiálnych odporúčaní, berúc do úvahy premenlivosť epidemiológia a riziko ochorenia v rôznych geografických oblastiach a cestovné podmienky. dukoral by nemali nahradiť štandardné ochranné opatrenia. v prípade hnačky opatrenia rehydratačný by mali byť podaný.

Spikevax (previously COVID-19 Vaccine Moderna) Európska únia - slovenčina - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) 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 - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

Infanrix Penta Európska únia - slovenčina - EMA (European Medicines Agency)

infanrix penta

glaxosmithkline biologicals s.a. - diphtheria toxoid, tetanus toxoid, bordetella pertussis antigens (pertussis toxoid, filamentous haemagglutinin, pertactin), poliovirus (inactivated) (type 1 (mahoney strain), type 2 (mef-1 strain), type 3 (saukett strain)), hepatitis b surface antigen - hepatitis b; tetanus; immunization; whooping cough; poliomyelitis; diphtheria - vakcíny - infanrix penta je indikovaný na primárne a posilňovacie očkovanie detí proti záškrtu, tetanu, pertussis, hepatitíde b a poliomyelitíde.

CHIROCAINE 5 mg/ml Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

chirocaine 5 mg/ml

abbvie s.r.o., slovensko - levobupivakaín - 01 - anaesthetica (lokÁlne)

Sufentanil Chiesi 5 µg/ml Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

sufentanil chiesi 5 µg/ml

chiesi pharmaceuticals gmbh, rakúsko - sufentanil - 65 - analgetica - anodyna

Sufentanil Chiesi 50 µg/ ml Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

sufentanil chiesi 50 µg/ ml

chiesi pharmaceuticals gmbh, rakúsko - sufentanil - 65 - analgetica - anodyna

Bupivakaín Accord 5 mg/ml injekčný roztok Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

bupivakaín accord 5 mg/ml injekčný roztok

accord healthcare polska sp. z o.o., poľsko - bupivakaín - 01 - anaesthetica (lokÁlne)

Bupivakaín Accord 2,5 mg/ml injekčný roztok Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

bupivakaín accord 2,5 mg/ml injekčný roztok

accord healthcare polska sp. z o.o., poľsko - bupivakaín - 01 - anaesthetica (lokÁlne)

Coxevac Európska únia - slovenčina - EMA (European Medicines Agency)

coxevac

ceva santé animale - inaktivovaná vakcína proti coxiella burnetii, kmeň nine mile - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

ProteqFlu-Te Európska únia - slovenčina - EMA (European Medicines Agency)

proteqflu-te

boehringer ingelheim vetmedica gmbh - clostridium tetani toxoid / vcp 2242 virus / vcp1529 virus / vcp1533 virus / vcp3011 vírus - immunologicals for equidae, live viral and inactivated bacterial vaccines, equine influenza virus + clostridium - kone - aktívna imunizácia koní štyroch mesiacov alebo starších proti chrípke koní na zníženie klinických príznakov a vylučovania vírusu po infekcii a proti tetanu na prevenciu úmrtnosti.