România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

sanofi-aventis deutschland gmbh - germania - insulina umane - sol. inj. in flacon - 100ui/ml - insuline si analogi insuline si analogi cu actiune rapida, injectabile

Uniunea Europeană - română - EMA (European Medicines Agency)

almirall s.a - tildrakizumab - psoriazis - imunosupresoare, inhibitori de interleukină, - ilumetri este indicat pentru tratamentul adulților cu forme moderate sau severe de psoriazis în plăci la care sunt candidați pentru terapia sistemică.

Uniunea Europeană - română - EMA (European Medicines Agency)

novartis europharm limited  - voretigene neparvovec - leber congenital amaurosis; retinitis pigmentosa - other ophthalmologicals - luxturna este indicat pentru tratamentul pacienților adulți și pacienți copii și adolescenți cu pierderea vederii din cauza moștenit distrofie retinei cauzate de confirmat biallelic rpe65 mutații și care au suficient de viabile celulele retinei.

Uniunea Europeană - română - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infecții pneumococice - vaccinuri - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. vezi secțiunile 4. 4 și 5. 1 pentru informații privind protecția împotriva serotipurilor pneumococice specifice. apexxnar should be used in accordance with official recommendations. .

Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

nanogen pharmceutical biotechnology company ltd. - peginterferon alfa-2a - solutie injectabila in seringa preumpluta - 180 mcg/0,5 ml

Uniunea Europeană - română - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - imunosupresoare - consultați documentul cu informații despre produs.

Uniunea Europeană - română - EMA (European Medicines Agency)

dompé biotec s.p.a. - darbepoetină alfa - kidney failure, chronic; anemia; cancer - preparate antianemice - tratamentul anemiei simptomatice asociate cu insuficiența renală cronică (crf) la adulți și copii. tratamentul anemiei simptomatice la pacienții adulți cu cancer non-mieloid administrează chimioterapie.

Uniunea Europeană - română - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabetul zaharat - medicamente utilizate în diabet - diabet zaharat în care este necesară tratamentul cu insulină. insulina umană winthrop rapidă, de asemenea, este potrivit pentru tratarea hyperglycaemic coma si cetoacidoza, precum şi pentru realizarea pre-, intra - şi stabilizare postoperatorie la pacienţii cu diabet zaharat.

Uniunea Europeană - română - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - diabetul zaharat - medicamente utilizate în diabet - diabet zaharat în care este necesară tratamentul cu insulină. insuman rapid este de asemenea potrivit pentru tratamentul hyperglycaemic comă şi cetoacidoza, precum şi pentru realizarea pre-, intra - şi stabilizare postoperatorie la pacienţii cu diabet zaharat.

Uniunea Europeană - română - 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 - vaccinuri - 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. utilizarea acestui vaccin ar trebui să fie în conformitate cu recomandările oficiale.