Bosulif Európai Unió - dán - EMA (European Medicines Agency)

bosulif

pfizer europe ma eeig - bosutinib (som monohydrat) - leukæmi, myeloid - antineoplastic agents, protein kinase inhibitors - bosulif er indiceret til behandling af voksne patienter med nyligt diagnosticeret kronisk fase (cp) philadelphia-kromosom-positiv kronisk myelogenous leukæmi (ph+ cml). cp, accelereret fase (ap), og blast fase (bp) ph+ cml, der tidligere er behandlet med en eller flere tyrosin kinase inhibitor(s) [tki(s)], og for hvem imatinib, nilotinib og dasatinib er ikke anset som egnede behandlingsmuligheder.

Champix Európai Unió - dán - EMA (European Medicines Agency)

champix

pfizer europe ma eeig - vareniclin - anvendelse af tobaksbrug - andre narkotika stoffer - champix er indiceret til rygestop hos voksne.

Ibrance Európai Unió - dán - EMA (European Medicines Agency)

ibrance

pfizer europe ma eeig  - palbociclib - bryst neoplasmer - antineoplastiske midler - ibrance er indiceret til behandling af hormon-receptor (hr) positiv, human epidermal growth factor receptor 2 (her2) negativ lokalt fremskreden eller metastatisk brystkræft:i kombination med en aromatasehæmmer, og i kombination med fulvestrant i kvinder, der har modtaget før den endokrine terapi. i præ - eller perimenopausal kvinder, den endokrine behandling bør kombineres med en luteiniserende hormon releasing hormon (lhrh) agonist.

Inlyta Európai Unió - dán - EMA (European Medicines Agency)

inlyta

pfizer europe ma eeig  - axitinib - carcinom, nyrecelle - protein kinase hæmmere - inlyta is indicated for the treatment of adult patients with advanced renal cell carcinoma (rcc) after failure of prior treatment with sunitinib or a cytokine.

Xalkori Európai Unió - dán - EMA (European Medicines Agency)

xalkori

pfizer europe ma eeig - crizotinib - carcinom, ikke-småcellet lunge - antineoplastiske midler - 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.

Vfend Európai Unió - dán - EMA (European Medicines Agency)

vfend

pfizer europe ma eeig - voriconazol - candidiasis; mycoses; aspergillosis - antimykotika til systemisk brug - voriconazol, er et bredt spektrum, triazol-svampemidler agent og er angivet i voksne og børn i alderen 2 år og derover, som følger:behandling af invasiv aspergillosis;behandling af i candidaemianon-neutropenic patienter, behandling af fluconazol-resistente alvorlige invasive candida infektioner (herunder c. krusei);behandling af alvorlige svampeinfektioner forårsaget af scedosporium spp.. og fusarium spp.. vfend bør administreres primært til patienter med progressive, eventuelt livstruende infektioner. profylakse af invasive svampeinfektioner i høj risiko allogen hæmatopoietisk stamcelletransplantation (hsct) modtagere.

Talzenna Európai Unió - dán - EMA (European Medicines Agency)

talzenna

pfizer europe ma eeig - talazoparib - bryst neoplasmer - antineoplastiske midler - talzenna er angivet som monoterapi til behandling af voksne patienter med germline brca1/2 mutationer, der har her2-negative lokalt fremskreden eller metastatisk brystkræft. 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 brystkræft skulle have været behandlet med en forudgående endokrine-baseret terapi, eller anses uegnet til at endokrine-baseret terapi.

Lorviqua Európai Unió - dán - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - carcinom, ikke-småcellet lunge - 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.

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

daurismo

pfizer europe ma eeig - glasdegib maleate - leukæmi, myeloid, akut - antineoplastiske midler - 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.

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

litfulo

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