Airexar Spiromax Európska únia - maltčina - EMA (European Medicines Agency)

airexar spiromax

teva b.v. - salmeterol, fluticasone propionate - pulmonary disease, chronic obstructive; asthma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - airexar spiromax huwa indikat għall-użu fl-adulti li għandhom 18-il sena 'l fuq biss. asthmaairexar spiromax is indicated for the regular treatment of patients with severe asthma where use of a combination product (inhaled corticosteroid and long-acting β2 agonist) is appropriate:- patients not adequately controlled on a lower strength corticosteroid combination productor- patients already controlled on a high dose inhaled corticosteroid and long-acting β2 agonist. mard pulmonari ostruttiv kroniku (copd)airexar spiromax huwa indikat għall-kura sintomatika ta ' pazjenti b'copd, bil-fev1.

Aranesp Európska únia - maltčina - EMA (European Medicines Agency)

aranesp

amgen europe b.v. - darbepoetin alfa - anemia; cancer; kidney failure, chronic - oħra antianemic preparazzjonijiet - kura ta 'anemija sintomatika assoċjata ma' insuffiċjenza renali kronika (crf) f'adulti u pazjenti pedjatriċi. kura ta ' anemija sintomatika f'pazjenti adulti bil-kanċer tumuri malinni mhux majelojdi li qed jirċievu l-kimoterapija.

Daliresp Európska únia - maltčina - EMA (European Medicines Agency)

daliresp

astrazeneca ab - roflumilast - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - daliresp huwa indikat għall-manutenzjoni trattament severi kronika eliminat pulmonari marda (copd) (fev1 bronchodilator wara inqas minn 50% mbassra) assoċjati ma ' bronchitis kroniċi fil-pazjenti adulti bi storja ta ' spiss exacerbations bħala żieda trattament bronchodilator.

Defitelio Európska únia - maltčina - EMA (European Medicines Agency)

defitelio

gentium s.r.l. - defibrotide - mard epatiku-okklussiv tal-vini - aġenti antitrombotiċi - defitelio huwa indikat għall-kura ta ' severi epatiċi okklussivi veno marda (vod) magħrufa wkoll bħala sinusojdali eliminat syndrome (sos) f'terapija haematopoietic-ċelloli staminali trapjant (hsct). huwa indikat fl-adulti u fl-adoloxxenti, tfal u trabi ' l fuq minn 1 xahar ta'età.

Edistride Európska únia - maltčina - EMA (European Medicines Agency)

edistride

astrazeneca ab - dapagliflozin propanediol monohydrate - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - drogi użati fid-dijabete - type 2 diabetes mellitusedistride is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. barra minn hekk għall-prodotti mediċinali oħra għat-trattament tad-dijabete tat-tip 2. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 u 5. heart failureedistride is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseedistride is indicated in adults for the treatment of chronic kidney disease.

Flebogamma DIF (previously Flebogammadif) Európska únia - maltčina - EMA (European Medicines Agency)

flebogamma dif (previously flebogammadif)

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.

Forxiga Európska únia - maltčina - EMA (European Medicines Agency)

forxiga

astrazeneca ab - dapagliflozin propanediol monohydrate - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - drogi użati fid-dijabete - type 2 diabetes mellitusforxiga is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. barra minn hekk għall-prodotti mediċinali oħra għat-trattament tad-dijabete tat-tip 2. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 u 5. heart failureforxiga is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseforxiga is indicated in adults for the treatment of chronic kidney disease.

Equilis Prequenza Európska únia - maltčina - EMA (European Medicines Agency)

equilis prequenza

intervet international bv - razez tal-virus ta 'l-influwenza taż-żwiemel: a / equine-2 / afrika t'isfel / 4/03, a / equine-2 / newmarket / 2/93 - virus tal-influwenza ekwina - Żwiemel - immunizzazzjoni attiva ta 'żwiemel minn sitt xhur ta' età kontra l-influwenza taż-żwiemel biex jitnaqqsu s-sinjali kliniċi u l-eskrezzjoni tal-virus wara l-infezzjoni.

Equilis Prequenza Te Európska únia - maltčina - EMA (European Medicines Agency)

equilis prequenza te

intervet international bv - razez tal-virus tal-influwenza ekwina: a / equine-2 / afrika t'isfel / 4/03, a / equine-2 / newmarket / 2/93, toxoid tat-tetnu - virus tal-influwenza ekwina + clostridium - Żwiemel - immunizzazzjoni attiva ta 'żwiemel minn sitt xhur ta' età kontra l-influwenza taż-żwiemel biex tnaqqas is-sinjali kliniċi u l-eskrezzjoni tal-virus wara l-infezzjoni, u immunizzazzjoni attiva kontra t-tetnu biex tevita l-mortalità.

Equilis Te Európska únia - maltčina - EMA (European Medicines Agency)

equilis te

intervet international bv - toxoid tat-tetnu - immunoloġiċi għall-equidae - Żwiemel - immunizzazzjoni attiva ta 'żwiemel li għandhom età ta' 6 xhur kontra t-tetnu biex tevita l-mortalità. bidu ta 'immunità: 2 ġimgħat wara l-vaċċinazzjoni primarja courseduration ta' l-immunità: 17-il xahar wara l-ewwel kors ta ' tilqim, 24 xahar wara l-ewwel revaċċinazzjoni.