Evropska unija - slovenščina - EMA (European Medicines Agency)

novartis vaccines and diagnostics s.r.l. - površinski antigeni virusa influence (hemaglutinin in nevraminidaza) seva a / viet nam / 1194/2004 (h5n1) - influenza, human; immunization; disease outbreaks - cepiva - aktivna imunizacija proti podtipu h5n1 virusa influenca a. , , this indication is based on immunogenicity data from healthy subjects from the age of 18 years onwards following administration of two doses of the vaccine containing a/vietnam/1194/2004 (h5n1)-like strain. , , prepandemic influenza vaccine (h5n1) novartis vaccines and diagnostic should be used in accordance with official recommendations.

Evropska unija - slovenščina - EMA (European Medicines Agency)

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - limfom, mantle cell - antineoplastična sredstva - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Evropska unija - slovenščina - EMA (European Medicines Agency)

vbi vaccines b.v. - površinski antigen hepatitisa b - hepatitis b - cepiva - prehevbri is indicated for active immunisation against infection caused by all known subtypes of the hepatitis b virus in adults. it can be expected that hepatitis d will also be prevented by immunisation with prehevbri as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection. the use of prehevbri should be in accordance with official recommendations.

Evropska unija - slovenščina - EMA (European Medicines Agency)

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 - cepiva - zdravilo infanrix penta je indicirano za primarno in obnovitveno cepljenje dojenčkov proti davici, tetanusu, oslovskemu kašlju, hepatitisu b in poliomielitisu.

Evropska unija - slovenščina - EMA (European Medicines Agency)

blue earth diagnostics ireland ltd - fluciclovine (18f) - prostatic neoplasms; radionuclide imaging - diagnostični radiofarmacevtiki - to zdravilo je samo za diagnostično uporabo. axumin je označen za positron emission tomografija (pet) slikanje za odkrivanje ponovitve raka na prostati pri moških odraslih z suma ponovitve, ki temelji na zvišan krvni prostato specifični antigen (psa) ravni po primarni kurativnega zdravljenja.

Evropska unija - slovenščina - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastična sredstva - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

servier pharma d.o.o. - amlodipin; atorvastatin; perindopril - filmsko obložena tableta - amlodipin 5 mg / 1 tableta  atorvastatin10 mg / 1 tableta  perindopril3,4 mg / 1 tableta; atorvastatin 10 mg / 1 tableta  perindopril3,4 mg / 1 tableta; perindopril 3,4 mg / 1 tableta - atorvastatin, amlodipin in perindopril

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

servier pharma d.o.o. - amlodipin; atorvastatin; perindopril - filmsko obložena tableta - amlodipin 10 mg / 1 tableta  atorvastatin20 mg / 1 tableta  perindopril6,79 mg / 1 tableta; atorvastatin 20 mg / 1 tableta  perindopril6,79 mg / 1 tableta; perindopril 6,79 mg / 1 tableta - atorvastatin, amlodipin in perindopril

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

servier pharma d.o.o. - amlodipin; atorvastatin; perindopril - filmsko obložena tableta - amlodipin 5 mg / 1 tableta  atorvastatin20 mg / 1 tableta  perindopril6,79 mg / 1 tableta; atorvastatin 20 mg / 1 tableta  perindopril6,79 mg / 1 tableta; perindopril 6,79 mg / 1 tableta - atorvastatin, amlodipin in perindopril

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

servier pharma d.o.o. - amlodipin; atorvastatin; perindopril - filmsko obložena tableta - amlodipin 5 mg / 1 tableta  atorvastatin20 mg / 1 tableta  perindopril3,4 mg / 1 tableta; atorvastatin 20 mg / 1 tableta  perindopril3,4 mg / 1 tableta; perindopril 3,4 mg / 1 tableta - atorvastatin, amlodipin in perindopril