欧州連合 - マルタ語 - EMA (European Medicines Agency)

sanofi pasteur - sars-cov-2 prefusion spike delta tm protein, recombinant (b.1.351 strain) - covid-19 virus infection - vaċċini - vidprevtyn beta is indicated as a booster for active immunisation to prevent covid-19 in adults who have previously received an mrna or adenoviral vector covid-19 vaccine (see sections 4. 2 u 5. 1 in product information document). l-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

instituto grifols s.a. - l-immunoglobulina normali umana - mucocutaneous lymph node syndrome; guillain-barre syndrome; bone marrow transplantation; purpura, thrombocytopenic, idiopathic; immunologic deficiency syndromes - sera immuni u immunoglobulini, - replacement therapy in adults, children and adolescents (0-18 years) in: , primary immunodeficiency syndromes with impaired antibody production;, hypogammaglobulinaemia and recurrent bacterial infections in patients with chronic lymphocytic luekaemia, in whom prophylactic antibiotics have failed;, hypogammaglobulinaemia and recurrent bacterial infections in plateau-phase-multiple-myeloma patients who failed to respond to pneumococcal immunisation;, hypogammaglobulinaemia in patients after allogenic haematopoietic-stem-cell transplantation (hsct);, congenital aids with recurrent bacterial infections. , immunomodulation in adults, children and adolescents (0-18 years) in: , primary immune thrombocytopenia (itp), in patients at high risk of bleeding or prior to surgery to correct the platelet count;, guillain barré syndrome;, kawasaki disease.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

novartis europharm limited - tisagenlecleucel - precursor b-cell lymphoblastic leukemia-lymphoma; lymphoma, large b-cell, diffuse - aġenti antineoplastiċi oħra - kymriah is indicated for the treatment of:• paediatric and young adult patients up to and including 25 years of age with b cell acute lymphoblastic leukaemia (all) that is refractory, in relapse post transplant or in second or later relapse. • adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl) after two or more lines of systemic therapy. • adult patients with relapsed or refractory follicular lymphoma (fl) after two or more lines of systemic therapy.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

merck sharp & dohme b.v. - daptomycin - gram-positive bacterial infections; bacteremia; soft tissue infections; endocarditis, bacterial - antibatteriċi għal użu sistemiku, - cubicin huwa indikat għat-trattament ta 'l-infezzjonijiet li ġejjin. adulti u pedjatriċi (1-17-il sena) ta ' pazjenti b'infezzjonijiet ikkumplikati tal-ġilda u tat-tessuti rotob (cssti). pazjenti adulti bi dritt naħat endokardite infettiva (rie) minn staphylococcus aureus. huwa rakkomandat li d-deċiżjoni li jintuża daptomycin għandha tieħu in kunsiderazzjoni l-suxxettibilità antibatterika ta 'l-organiżmu u għandha tkun ibbażata fuq parir ta' espert. adulti u pedjatriċi (1-17-il sena) il-pazjenti bil-batterimja minn staphylococcus aureus (sab). fl-adulti, l-użu fl-batterimja għandha tkun assoċjata ma 'rie jew ma' cssti, filwaqt li fil-pazjenti pedjatriċi, l-użu fl-batterimja għandu jkun assoċjat ma ' cssti. daptomycin huwa attiv kontra batteri gram posittivi biss. imħallat ta 'l-infezzjonijiet fejn gram negattivi u/jew ċerti tipi ta' batterji anerobiċi huma suspettati, cubicin għandu jingħata flimkien ma ' sustanza anti batterjali xierqa(i). għandha tingħata kunsiderazzjoni għall-gwida uffiċjali dwar l-użu xieraq ta ' sustanzi antibatteriċi.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

takeda gmbh - dengue virus, serotype 2, expressing dengue virus, serotype 1, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 3, surface proteins, live, attenuated, dengue virus, serotype 2, expressing dengue virus, serotype 4, surface proteins, live, attenuated, dengue virus, serotype 2, live, attenuated - Ħnieżer - vaċċini - qdenga is indicated for the prevention of dengue disease in individuals from 4 years of age. the use of qdenga should be in accordance with official recommendations.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

baxalta innovations gmbh - vonicog alfa - mard von willebrand - sustanzi kontra l-emorraġija - veyvondi huwa indikat fl-adulti (età ta '18-il sena u akbar) bl-mard ta' von willebrand (vwd), meta desmopressin (ddavp) il-kura waħdu huwa ineffettivi jew mhux indikat għal - kura ta 'emorraġija u kirurġija ta' fsada - prevenzjoni tal-kirurġika emorraġija. veyvondi m'għandux jintuża fil-kura ta'l-emofilja a.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

mylan s.a.s. - docetaxel - head and neck neoplasms; carcinoma, non-small-cell lung; adenocarcinoma; prostatic neoplasms; breast neoplasms - aġenti antineoplastiċi - kura tal-kanċer tas-sider, forom speċjali ta 'kanċer tal-pulmun (kanċer tal-pulmun mhux ta' ċelluli żgħar), kanċer tal-prostata, kanċer gastriku jew kanċer tar-ras u l-għonq.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

csl behring gmbh - human alpha1-proteinase inhibitor - genetic diseases, inborn; lung diseases - sustanzi kontra l-emorraġija - respreeza huwa indikat għal trattament ta 'manteniment, biex inaqqas il-progressjoni ta' enfisema f'adulti b'defiċjenza dokumentata ta 'inibitur ta' alpha1-proteinase (e. ġenotipi pizz, piz (null), pi (null, null), pisz). il-pazjenti għandhom ikunu taħt l-aħjar trattament farmakoloġiku u mhux farmakoloġiku u juru evidenza ta 'mard tal-pulmun progressiv (e. inqas volum espiratorju furzat kull sekonda (fev1) mbassra, imfixkla kapaċità bil-mixi jew żdied in-numru ta ' l-exacerbations) kif evalwat mill-professjonista ta ' esperjenza fit-trattament tad-defiċjenza ta ' inibitur ta ' 1-proteinase.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - karċinoma, pulmun mhux taċ-Ċellula Żgħira - aġenti antineoplastiċi - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.

欧州連合 - マルタ語 - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - majloma multipla - aġenti antineoplastiċi - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.