Europäische Union - Maltesisch - EMA (European Medicines Agency)

chiesi farmaceutici s.p.a. - beclometasone dipropionate, formoterol fumarate dihydrate, glycopyrronium - mard tal-pulmun, obstructive kronika - mediċini għall-imblokkar tal-passaġġ tan-nifs mard, - trattament ta ' manutenzjoni fil-pazjenti adulti ma moderat severi kronika eliminat pulmonari marda (copd) li m'humiex ittrattati adegwatament mill-għaqda tal-corticosteroid bin-nifs u a twila u jaġixxu beta2-agonist (għall-effetti fuq is-sintomi kontroll u prevenzjoni ta ' exacerbations ara taqsima 5.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

laboratoire aguettant - sufentanil citrate - uġigħ - anestetiċi - dzuveo is indicated for the management of acute moderate to severe pain in adult patients.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

kyowa kirin holdings b.v. - mogamulizumab - sezary syndrome; mycosis fungoides - aġenti antineoplastiċi - poteligeo huwa indikat għall-kura ta ' pazjenti adulti b'mycosis fungoides (mf) jew sézary sindromu (ss) li rċevew ta'l-anqas qabel terapija sistemika.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

astellas pharma europe b.v. - gilteritinib fumarate - lewkimja, mijelojda, akuta - aġenti antineoplastiċi - xospata huwa indikat bħala monoterapija għall-kura ta ' pazjenti adulti li rkadew jew refrattorji lewkimja majelojde akuta (aml) b'flt3 mutazzjoni.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

shionogi b.v. - cefiderocol sulfate tosilate - gram-negattivi infezzjonijiet tal-batterji - antibatteriċi għal użu sistemiku, - fetcroja huwa indikat għall-kura ta 'infezzjonijiet minħabba aerobiċi gram-negattivi organiżmi fl-adulti bil-limitat għażliet ta' trattament (ara sezzjonijiet 4. 2, 4. 4 u 5. għandha tingħata kunsiderazzjoni għall-gwida uffiċjali dwar l-użu xieraq ta ' sustanzi antibatteriċi.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

virbac s.a. - tulathromycin - antibacterials għal użu sistemiku - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. the product should only be used if pigs are expected to develop the disease within 2–3 days. nagħaġ: trattament tal-istadji bikrija ta 'pododermatite infettiva (taħsir tas-sieq) assoċjat ma' dichelobacter nodosus virulenti li jeħtieġ trattament sistemiku.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

kite pharma eu b.v. - autologous peripheral blood t cells cd4 and cd8 selected and cd3 and cd28 activated transduced with retroviral vector expressing anti-cd19 cd28/cd3-zeta chimeric antigen receptor and cultured (brexucabtagene autoleucel) - limfoma, mantle-cell - aġenti antineoplastiċi - mantle cell lymphomatecartus is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl) after two or more lines of systemic therapy including a bruton’s tyrosine kinase (btk) inhibitor. acute lymphoblastic leukaemiatecartus is indicated for the treatment of adult patients 26 years of age and above with relapsed or refractory b-cell precursor acute lymphoblastic leukaemia (all).

Europäische Union - Maltesisch - EMA (European Medicines Agency)

elanco gmbh - tulathromycin - antibacterials għal użu sistemiku - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. the product should only be used if pigs are expected to develop the disease within 2–3 days. nagħaġ: trattament tal-istadji bikrija ta 'pododermatite infettiva (taħsir tas-sieq) assoċjat ma' dichelobacter nodosus virulenti li jeħtieġ trattament sistemiku.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

vmd n.v. - tulathromycin - antibacterials for systemic use, macrolides - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. the product should only be used if pigs are expected to develop the disease within 2–3 days. nagħaġ: trattament tal-istadji bikrija ta 'pododermatite infettiva (taħsir tas-sieq) assoċjat ma' dichelobacter nodosus virulenti li jeħtieġ trattament sistemiku.

Europäische Union - Maltesisch - EMA (European Medicines Agency)

dechra regulatory b.v. - tulathromycin - antibacterials għal użu sistemiku - cattle; pigs; sheep - cattle: treatment and metaphylaxis of bovine respiratory disease (brd) associated with mannheimia haemolytica, pasteurella multocida, histophilus somni and mycoplasma bovis susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. treatment of infectious bovine keratoconjunctivitis (ibk) associated with moraxella bovis susceptible to tulathromycin. pigs: treatment and metaphylaxis of swine respiratory disease (srd) associated with actinobacillus pleuropneumoniae, pasteurella multocida, mycoplasma hyopneumoniae, haemophilus parasuis and bordetella bronchiseptica susceptible to tulathromycin. il-preżenza tal-marda fil-merħla għandha tiġi stabbilita qabel it-trattament metaphylactic. the product should only be used if pigs are expected to develop the disease within 2–3 days. nagħaġ: trattament tal-istadji bikrija ta 'pododermatite infettiva (taħsir tas-sieq) assoċjat ma' dichelobacter nodosus virulenti li jeħtieġ trattament sistemiku.