Lumeblue (previously known as Methylthioninium chloride Cosmo) Европска Унија - Мелтешки - EMA (European Medicines Agency)

lumeblue (previously known as methylthioninium chloride cosmo)

alfasigma s.p.a. - methylthioninium chloride - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Apexxnar Европска Унија - Мелтешки - EMA (European Medicines Agency)

apexxnar

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - infezzjonijiet pnewmokokkali - vaċċini - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. ara t-taqsimiet 4. 4 u 5. 1 għal informazzjoni dwar il-protezzjoni kontra serotipi pnewmokokkiċi speċifiċi. apexxnar should be used in accordance with official recommendations. .

Filsuvez Европска Унија - Мелтешки - EMA (European Medicines Agency)

filsuvez

amryt pharmaceuticals dac - dry extract from birch bark (der 5-10 : 1), extraction solvent n-heptane 95% (w/w) - epidermolysis bullosa dystrophica; epidermolysis bullosa, junctional - preparazzjonijiet għat-trattament ta 'feriti u ulċeri - treatment of partial thickness wounds associated with dystrophic and junctional epidermolysis bullosa (eb) in patients 6 months and older.

Rivastigmine 3M Health Care Ltd Европска Унија - Мелтешки - EMA (European Medicines Agency)

rivastigmine 3m health care ltd

3m health care limited - rivastigmine - marda ta 'alzheimer - psychoanaleptics, , anticholinesterases - trattament sintomatiku ta 'dimenzja ta' alzheimer ħafifa għal moderatament gravi.

Adasuve Европска Унија - Мелтешки - EMA (European Medicines Agency)

adasuve

ferrer internacional s.a. - loxapine - schizophrenia; bipolar disorder - sistema nervuża - adasuve huwa indikat għall-kontroll rapidu ta 'aġitazzjoni ħafifa għal moderata f'pazjenti adulti bi skiżofrenja jew disturb bipolari. il-pazjenti għandhom jirċievu trattament regolari immedjatament wara l-kontroll ta 'sintomi ta' aġitazzjoni akuta.

Amyvid Европска Унија - Мелтешки - EMA (European Medicines Agency)

amyvid

eli lilly nederland b.v. - florbetapir (18f) - radjonuklidi imaging - radjofarmaċewtiċi dijanjostiċi - dan il-prodott mediċinali huwa għal użu dijanjostiku biss. amyvid hija prodott radjufarmaċewtiku indikat għall-positron emission tomography (pet) tal-immaġini tal-β-amyloid neuritic-plakka densità fl-imħuħ tal-pazjenti adulti b'indeboliment konjittiv li jkunu qed jiġu evalwati għall-marda ta'alzheimer (ad) u kawżi oħra ta ' indeboliment konjittiv. amyvid għandhom jintużaw flimkien ma ' evalwazzjoni klinika. negattiv scan jindika skarsa jew l-ebda plakek, li mhuwiex konsistenti mal-dijanjosi tal ad.

Arzerra Европска Унија - Мелтешки - EMA (European Medicines Agency)

arzerra

novartis europharm ltd - ofatumumab - lewkimja, linfokitika, kronika, b-Ċellula - antikorpi monoklonali - ma kienux trattati qabel lewkimja limfoċitika kronika (cll): arzerra flimkien ma 'chlorambucil jew bendamustine huwa indikat għall-kura ta' pazjenti b'cll li ma rċevew terapija minn qabel u li mhumiex eliġibbli għall-fludarabine-terapija bbażata fuq. rkadew cll: arzerra huwa indikat flimkien ma 'fludarabine u cyclophosphamide għat-trattament ta' pazjenti adulti b'all rikadut cll. refrattarji cll: arzerra huwa indikat għall-kura ta cll f'pazjenti li huma refrattarji għal pazjenti b'b-ll u alemtuzumab.

Bretaris Genuair Европска Унија - Мелтешки - EMA (European Medicines Agency)

bretaris genuair

covis pharma europe b.v. - aclidinium bromide - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - bretaris genuair huwa indikat bħala trattament ta 'manteniment tal-bronkodilatur biex itaffi s-sintomi f'pazjenti adulti b'mard pulmonari ostruttiv kroniku (copd).

Budesonide/Formoterol Teva Европска Унија - Мелтешки - EMA (European Medicines Agency)

budesonide/formoterol teva

teva pharma b.v. - budesonide, formoterol fumarate dihydrate - pulmonary disease, chronic obstructive; asthma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - budesonide / formoterol teva huwa indikat fl-adulti ta '18-il sena' l fuq biss. asthmabudesonide/formoterol teva huwa indikat fit-trattament regolari ta ' l-ażżma, fejn l-użu tal-kombinazzjoni (kortikosterojdi meħuda man-nifs u li jaħdem fit-tul β2 adrenoceptor agonist) huwa xieraq:f'pazjenti li mhumiex adegwatament ikkontrollati bil-kortikosterojdi meħuda man-nifs u l - "kif meħtieġ" man-nifs qasir waqt li jaġixxi β2 adrenoceptor agonisti. fjorin pazjenti li diġà ikkontrollati adegwatament fuq iż-żewġ kortikosterojdi meħuda man-nifs u li jaħdem fit-tul β2 adrenoceptor agonisti. copdsymptomatic-trattament ta ' pazjenti b'indeboliment serju copd (fev1 < 50% mbassra-normal) u l-istorja tal-aggravar tal-attakki ripetuti, li għandhom sinifikanti sintomi minkejja regolari it-terapija b'taġixxi fit-tul bronkodilataturi.

Budesonide/Formoterol Teva Pharma B.V. Европска Унија - Мелтешки - EMA (European Medicines Agency)

budesonide/formoterol teva pharma b.v.

teva pharma b.v. - budesonide, formoterol - ażma - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - budesonide / formoterol teva pharma b. hija indikata fl-adulti ta '18-il sena u akbar biss. asthmabudesonide/formoterol teva pharma b. is indicated in the regular treatment of asthma, where use of a combination (inhaled corticosteroid and long-acting β2 adrenoceptor agonist) is appropriate: orin patients not adequately controlled with inhaled corticosteroids and “as needed” inhaled short-acting β2 adrenoceptor agonists. in patients already adequately controlled on both inhaled corticosteroids and long-acting β2 adrenoceptor agonists.