Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig  - palbociclib - bröst-neoplasmer - antineoplastiska medel - ibrance är indicerat för behandling av hormon receptor (hr) positiv, human epidermal growth factor receptor 2 (her2) negativa lokalt avancerad eller metastaserad bröstcancer:i kombination med en aromatashämmare, i kombination med fulvestrant i kvinnor som har fått innan endokrin terapi. i pre - eller perimenopausala kvinnor, endokrin terapi bör kombineras med en luteinizing hormone releasing hormone (gnrh) agonist.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig - crizotinib - carcinom, non-small cell lung - antineoplastiska medel - xalkori as monotherapy is indicated for:the first‑line treatment of adults with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with previously treated anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with ros1‑positive advanced non‑small cell lung cancer (nsclc)the treatment of paediatric patients (age ≥6 to.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig - talazoparib - bröst-neoplasmer - antineoplastiska medel - talzenna är indicerat som monoterapi för behandling av vuxna patienter med könsceller brca1/2 mutation, som har her2-negativa lokalt avancerad eller metastaserande bröstcancer. patients should have been previously treated with an anthracycline and/or a taxane in the (neo)adjuvant, locally advanced or metastatic setting unless patients were not suitable for these treatments. patienter med hormon receptor (hr)-positiv bröstcancer bör ha behandlats med en före endokrina-baserad terapi, eller anses vara olämpliga för endokrina-baserad terapi.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig - lorlatinib - carcinom, non-small cell lung - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig - dacomitinib monohydrat - carcinom, non-small cell lung - antineoplastiska medel - vizimpro, som monoterapi är indicerat för första linjens behandling av vuxna patienter med lokalt avancerad eller metastaserad icke småcellig lungcancer (nsclc) med epidermal growth factor receptor (egfr) med aktiverande mutationer.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig  - crisaborole - dermatit, atopisk - andra dermatologiska preparat - staquis är indicerat för behandling av mild till måttlig atopisk dermatit hos vuxna och pediatriska patienter från 2 års ålder ≤ 40% av kroppsytan (bsa) som påverkas.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig - glasdegib maleate - leukemi, myeloid, akut - antineoplastiska medel - 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.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig  - pegfilgrastim - neutropeni - immunstimulatorer, - reducera durationen av neutropeni och incidensen av febril neutropeni hos vuxna patienter som behandlas med cytotoxisk kemoterapi för malignitet (med undantag för kronisk myeloisk leukemi och myelodysplastiska syndrom).

Európai Unió - svéd - EMA (European Medicines Agency)

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.

Európai Unió - svéd - EMA (European Medicines Agency)

pfizer europe ma eeig - respiratory syncytial virus, subgroup a, stabilized prefusion f protein / respiratory syncytial virus, subgroup b, stabilized prefusion f protein - respiratoriska syncytialvirusinfektioner - vacciner - 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. se avsnitt 4. 2 och 5. active immunisation of individuals 60 years of age and older for the prevention of lower respiratory tract disease caused by rsv. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.