Prepandemic Influenza Vaccine (H5N1) (Split Virion, Inactivated, Adjuvanted) GlaxoSmithKline Biologicals Europese Unie - Sloveens - EMA (European Medicines Agency)

prepandemic influenza vaccine (h5n1) (split virion, inactivated, adjuvanted) glaxosmithkline biologicals

glaxosmithkline biologicals s.a. - deaktiviran virus gripe, ki vsebuje antigen: a / vietnam / 1194/2004 (h5n1), podoben sevu (nibrg-14) - influenza, human; immunization; disease outbreaks - cepiva - aktivna imunizacija proti podtipu h5n1 virusa influenca a. ta navedba temelji na immunogenicity podatkov iz zdravih predmetov iz 18. leta starosti dalje po uporabi zdravila dva odmerka cepiva, pripravljeni iz a/vietnam/1194/2004 nibrg-14 (h5n1) (glej točko 5. prepandemic cepiva proti gripi (h5n1) (split virion, inaktivirano, adjuvanted) glaxosmithkline biologicals 3. 75 µg je treba uporabljati v skladu z uradnimi smernice.

Twinrix Adult Europese Unie - Sloveens - EMA (European Medicines Agency)

twinrix adult

glaxosmithkline biologicals s.a. - hepatitis a virus (inaktivirano), hepatitis b površinski antigen - hepatitis b; hepatitis a; immunization - cepiva - zdravilo twinrix adult je indicirano za uporabo pri neimunskih odraslih in mladostnikih, starih 16 let ali več, ki jim grozi okužba s hepatitisom a in hepatitisom b.

Axumin Europese Unie - Sloveens - EMA (European Medicines Agency)

axumin

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.

Locametz Europese Unie - Sloveens - EMA (European Medicines Agency)

locametz

novartis europharm limited  - gozetotide - radionuklidno slikanje - diagnostični radiofarmacevtiki - to zdravilo je samo za diagnostično uporabo. locametz, after radiolabelling with gallium 68, is indicated for the detection of prostate specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high risk pca prior to primary curative therapy,suspected pca recurrence in patients with increasing levels of serum prostate specific antigen (psa) after primary curative therapy,identification of patients with psma positive progressive metastatic castration resistant prostate cancer (mcrpc) for whom psma targeted therapy is indicated (see section 4.

Pylclari Europese Unie - Sloveens - EMA (European Medicines Agency)

pylclari

curium pet france - piflufolastat (18f) - prostatične neoplazme - diagnostični radiofarmacevtiki - to zdravilo je samo za diagnostično uporabo. pylclari is indicated for the detection of prostate-specific membrane antigen (psma) positive lesions with positron emission tomography (pet) in adults with prostate cancer (pca) in the following clinical settings:primary staging of patients with high-risk pca prior to initial curative therapy,to localize recurrence of pca in patients with a suspected recurrence based on increasing serum prostate-specific antigen (psa) levels after primary treatment with curative intent. pylclari is indicated for use with positron emission tomography (pet).

Ceftazidim Hospira 2 g prašek za raztopino za injiciranje/infundiranje Slovenië - Sloveens - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

ceftazidim hospira 2 g prašek za raztopino za injiciranje/infundiranje

hospira uk ltd - ceftazidim - prašek za raztopino za injiciranje/infundiranje - ceftazidim 2000 mg / 1 viala - ceftazidim