Pemetrexed Pfizer (previously Pemetrexed Hospira) Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

pemetrexed pfizer (previously pemetrexed hospira)

pfizer europe ma eeig - pemetrexed disodium, pemetrexed disodium hemipentahydrate - carcinoma, non-small-cell lung; mesothelioma - antinavikiniai vaistai - malignant pleural mesotheliomapemetrexed pfizer in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancerpemetrexed pfizer in combination with cisplatin is indicated for the first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. pemetrexed pfizer is indicated as monotherapy for the maintenance treatment of locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology in patients whose disease has not progressed immediately following platinum-based chemotherapy. pemetrexed pfizer is indicated as monotherapy for the second-line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology.

Pemetrexed Pfizer (previously known as Pemetrexed Hospira UK Limited) Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

pemetrexed pfizer (previously known as pemetrexed hospira uk limited)

pfizer europe ma eeig - pemetrexed ditromethamine - carcinoma, non-small-cell lung; mesothelioma - folio rūgšties analogai, antimetabolites - piktybinė pleuros mesotheliomapemetrexed hospira uk limited " kartu su cisplatina skiriamas gydymas chemoterapija naivu pacientams, sergantiems unresectable piktybinės pleuros mezoteliomos. nesmulkialąstelinio plaučių cancerpemetrexed hospira uk limited " kartu su cisplatina skiriamas pirmos eilės gydymas pacientams, sergantiems lokaliai išplitusio arba metastazavusio nesmulkialąstelinio plaučių vėžio, išskyrus daugiausia suragėjusių ląstelių histologija (žr. vcs 5 skirsnis. pemetrexed hospira uk limited yra nurodyta kaip monotherapy priežiūros gydymas lokaliai išplitusio arba metastazavusio nesmulkialąstelinio plaučių vėžio, išskyrus daugiausia suragėjusių ląstelių histologija pacientams, kurių liga nebuvo vyko iš karto po platinos pagrindu chemoterapija (žr. vcs 5 skirsnis. pemetrexed hospira uk limited yra nurodyta kaip monotherapy, antrą-line pacientų, sergančių vietiškai išplitusio arba metastazavusio nesmulkialąstelinio plaučių vėžio, išskyrus daugiausia suragėjusių ląstelių histologija (žr. vcs 5 skirsnis.

Oxbryta Europos Sąjunga - lietuvių - 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.

Inlyta Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

inlyta

pfizer europe ma eeig  - aksitinibas - karcinoma, inkstų ląstelė - baltymų kinazės inhibitoriai - 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.

Pregabalin Pfizer Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

pregabalin pfizer

upjohn eesv - pregabalinas - anxiety disorders; epilepsy - antiepileptics, - neuropatinis painpregabalin pfizer nurodomas gydymo periferinis ir centrinis neuropatinis skausmas suaugusieji. epilepsypregabalin "pfizer" žymi kaip adjunctive terapija suaugusiems, turintiems dalinį konfiskavimą su ar be antrinės apibendrinimas. generalizuoto nerimo disorderpregabalin "pfizer" yra nurodyta, gydant generalizuoto nerimo sutrikimas (gad) suaugusiems.

Xalkori Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

xalkori

pfizer europe ma eeig - krizotinibas - karcinoma, nesmulkiųjų ląstelių skausmas - antinavikiniai vaistai - 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.

Sutent Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

sutent

pfizer limited - sunitinibas - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antinavikiniai vaistai - gastrointestinal stromal tumour (gist)sutent is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib mesilate treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sutent is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sutent is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours with disease progression in adults. experience with sutent as first-line treatment is limited (see section 5.

Zavicefta Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

zavicefta

pfizer ireland pharmaceuticals - avibactam sodium, ceftazidime pentahydrate - pneumonia, bacterial; soft tissue infections; pneumonia; urinary tract infections; gram-negative bacterial infections - antibacterials sisteminio naudojimo, - zavicefta is indicated in adults and paediatric patients aged 3 months and older for the treatment of the following infections:complicated intra-abdominal infection (ciai)complicated urinary tract infection (cuti), including pyelonephritishospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap)treatment of patients with bacteraemia that occurs in association with, or is suspected to be associated with, any of the infections listed above. zavicefta is also indicated for the treatment of infections due to aerobic gram-negative organisms in adults and paediatric patients aged 3 months and older with limited treatment options. reikėtų atsižvelgti į oficialius nurodymus, kaip tinkamai naudoti antibakterinių veiksnių.

Lorviqua Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - karcinoma, nesmulkiųjų ląstelių skausmas - 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 Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

daurismo

pfizer europe ma eeig - glasdegib maleate - leukemija, mieloidas, ūmus - antinavikiniai vaistai - 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.