Vizimpro Európai Unió - máltai - EMA (European Medicines Agency)

vizimpro

pfizer europe ma eeig - dacomitinib monohydrate - karċinoma, pulmun mhux taċ-Ċellula Żgħira - aġenti antineoplastiċi - vizimpro, bħala monoterapija, huwa indikat għall-kura tal-ewwel linja ta 'pazjenti adulti b'lokalment avvanzat jew dak metastatiku li mhux ta' ċelluli żgħar kanċer tal-pulmun (nsclc) mar-riċettur tal-fattur tat-tkabbir epidermali (egfr) mutazzjonijiet li jattivaw.

Staquis Európai Unió - máltai - EMA (European Medicines Agency)

staquis

pfizer europe ma eeig  - crisaborole - dermatite, atopika - preparazzjonijiet oħra dermatoloġiċi - staquis huwa indikat għall-kura ta ħfief għal moderati-dermatite atopika fl-adulti u f'pazjenti pedjatriċi minn 2-il sena ma ' ≤ 40% - superfiċje tal-ġisem (bsa) milquta.

Daurismo Európai Unió - máltai - EMA (European Medicines Agency)

daurismo

pfizer europe ma eeig - glasdegib maleate - lewkimja, mijelojda, akuta - aġenti antineoplastiċi - daurismo is indicated, in combination with low-dose cytarabine, for the treatment of newly diagnosed de novo or secondary acute myeloid leukaemia (aml) in adult patients who are not candidates for standard induction chemotherapy.

Cibinqo Európai Unió - máltai - EMA (European Medicines Agency)

cibinqo

pfizer europe ma eeig  - abrocitinib - dermatite, atopika - preparazzjonijiet oħra dermatoloġiċi - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

Ngenla Európai Unió - máltai - EMA (European Medicines Agency)

ngenla

pfizer europe ma eeig - somatrogon - growth and development - pitwitarja u l-assi ipotalamika-ormoni u analogi - indicated for the long-term treatment of paediatric patients with growth disturbance due to insufficient secretion of growth hormone.

Oxbryta Európai Unió - máltai - EMA (European Medicines Agency)

oxbryta

pfizer europe ma eeig  - voxelotor - anemia; anemia, hemolytic; anemia, sickle cell - other hematological agents - oxbryta is indicated for the treatment of haemolytic anaemia due to sickle cell disease (scd) in adults and paediatric patients 12 years of age and older as monotherapy or in combination with hydroxycarbamide.

Apexxnar Európai Unió - máltai - EMA (European Medicines Agency)

apexxnar

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 - infezzjonijiet pnewmokokkali - vaċċini - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. ara t-taqsimiet 4. 4 u 5. 1 għal informazzjoni dwar il-protezzjoni kontra serotipi pnewmokokkiċi speċifiċi. apexxnar should be used in accordance with official recommendations. .

Abrysvo Európai Unió - máltai - EMA (European Medicines Agency)

abrysvo

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - infezzjonijiet ta 'virus sintetiku respiratorju - vaċċini - abrysvo is indicated for:passive protection against lower respiratory tract disease caused by respiratory syncytial virus (rsv) in infants from birth through 6 months of age following maternal immunisation during pregnancy. ara t-taqsimiet 4. 2 u 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. l-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

Litfulo Európai Unió - máltai - EMA (European Medicines Agency)

litfulo

pfizer europe ma eeig - ritlecitinib tosilate - alopecia areata - immunosoppressanti - litfulo is indicated for the treatment of severe alopecia areata in adults and adolescents 12 years of age and older.

ProMeris Európai Unió - máltai - EMA (European Medicines Agency)

promeris

pfizer limited  - metaflumizone - ektoparasitaċidali għall-użu topiku, inklużi. insettiċidi - qtates - trattament u prevenzjoni ta 'infestazzjonijiet tal-briegħed (ctenocephalides canis u c. felis) fil-qtates. il-prodott mediċinali veterinarju jista 'jintuża bħala parti minn strateġija ta' trattament għal dermatite tal-allerġija tal-briegħed (fad).