Unió Europea - maltès - EMA (European Medicines Agency)

novo nordisk a/s - insulin aspart - diabetes mellitus - drugs used in diabetes, insulins and analogues for injection, fast-acting - trattament tad-dijabete mellitus f'adulti, adolexxenti u tfal ta 'sena u aktar.

Unió Europea - maltès - EMA (European Medicines Agency)

gilead sciences ireland uc - ledipasvir, sofosbuvir - epatite Ċ, kronika - antivirali għal użu sistemiku - harvoni is indicated for the treatment of chronic hepatitis c (chc) in adult and paediatric patients aged 3 years and above (see sections 4. 2, 4. 4 u 5. għall-vajrus tal-epatite Ċ (hcv) ġenotip-attività speċifika ara sezzjonijiet 4. 4 u 5.

Unió Europea - maltès - EMA (European Medicines Agency)

csl behring gmbh - immunoglobulina normali umana (scig) - sindromi ta 'defiċjenza immunoloġika - sera immuni u immunoglobulini, - replacement therapy in adults, children and adolescents (0-18 years) in:- primary immunodeficiency syndromes with impaired antibody production (see section 4. - secondary immunodeficiencies (sid) in patients who suffer from severe or recurrent infections, ineffective antimicrobial treatment and either proven specific antibody failure (psaf)* or serum igg level of.

Unió Europea - maltès - EMA (European Medicines Agency)

bayer animal health gmbh - imidakloprid, moksidektin - prodotti kontra l-parassiti, insettiċidi u repellenti - dogs; cats; ferrets - dogsfor klieb li qed isofru minn, jew huma f'riskju minn infezzjonijiet kawżati minn parassiti diversi:it-trattament u l-prevenzjoni tal-infestazzjoni mill-briegħed (ctenocephalides felis),trattament tal-qamel li jigdem (trichodectes canis),trattament ta ' infestazzjoni dudu tal-widna (otodectes cynotis), sarcoptic mange (ikkawżata minn sarcoptes scabiei var. canis), 'domodikosis (ikkawżata minn demodex canis),il-prevenzjoni tal-heartworm disease (l3 u l-larva l4 tad-dirofilaria immitis),trattament ta jiċċirkola microfilariae (dirofilaria immitis),il-kura ta' cutaneous dirofilariosis (adulti l-istadji tal-dirofilaria repens)il-prevenzjoni tal-ġilda dirofilariosis (larva l3 tal-dirofilaria repens),it-tnaqqis tal jiċċirkola microfilariae (dirofilaria repens),il-prevenzjoni tal-angiostrongylosis (larva l4 u l-adulti immaturi ta 'angiostrogylus vasorum),it-trattament ta' angiostrogylus vasorum u crenosoma vulpis,il-prevenzjoni tal-spirocercosis (spirocerca lupi),it-trattament tal-eucoleus (sin. capillaria) boehmi (adulti),il-kura ta 'l-għajn worm thelazia callipaeda (adulti),il-kura ta' infezzjonijiet bl-ħniex gastro-intestinali (larva l4, adulti immaturi u l-adulti tal-toxocara canis, ancylostoma caninum u uncinaria stenocephala, adulti tat-toxascaris leonina u trichuris vulpis). il-prodott jista 'jintuża bħala parti minn strateġija ta' trattament għal dermatite tal-allerġija tal-briegħed (fad). catsfor-qtates li jbatu minn, jew huma f'riskju minn infezzjonijiet kawżati minn parassiti diversi:it-trattament u l-prevenzjoni tal-infestazzjoni mill-briegħed (ctenocephalides felis),trattament ta 'infestazzjoni dudu tal-widna (otodectes cynotis),it-trattament tal-notoedric mange (notoedres cati),il-kura ta' l-lungworm eucoleus aerophilus (sin. capillaria aerophila) (adulti),il-prevenzjoni tal-lungworm-marda (l3/larva l4 ta'aelurostrongylus abstrusus),il-kura ta 'l-lungworm aelurostrongylus abstrusus (adulti),il-kura ta' l-għajn worm thelazia callipaeda (adulti),il-prevenzjoni tal-heartworm disease (l3 u l-larva l4 tad-dirofilaria immitis),trattament ta ' infezzjonijiet b'nematodi gastrointestinali (larva l4, adulti immaturi u l-adulti tal-toxocara cati u ancylostoma tubaeforme). il-prodott jista 'jintuża bħala parti minn strateġija ta' trattament għal dermatite tal-allerġija tal-briegħed (fad). ferretsfor l-inmsa li qed isofru minn, jew huma f'riskju minn infezzjonijiet kawżati minn parassiti diversi:it-trattament u l-prevenzjoni tal-infestazzjoni mill-briegħed (ctenocephalides felis),il-prevenzjoni tal-heartworm disease (l3 u l-larva l4 tad-dirofilaria immitis).

Unió Europea - maltès - EMA (European Medicines Agency)

intervet international bv - vaċċin tal-vajrus tal-bluetongue, serotip 8 (mhux attivat) - vaċċini virali inattivati, virus tal-bluetongue, nagĦaĠ - sheep; cattle - cattle to stimulate active immunity in sheep from 6 weeks of age against bluetongue virus serotype 8 to reduce viraemia sheep to stimulate active immunity in sheep from 1 month of age against bluetongue virus serotype 8 to prevent viraemia,.

Unió Europea - maltès - EMA (European Medicines Agency)

ceva santé animale - benazepril hydrochloride, spironolactone - sistema kardjovaskulari - klieb - għat-trattament ta 'insuffiċjenza tal-qalb konġestiva kkawżata minn mard valvulari klementi deġenerattiv fil-klieb (b'appoġġ dijuretiku kif xieraq).

Unió Europea - maltès - EMA (European Medicines Agency)

janssen-cilag international nv - ibrutinib - lymphoma, mantle-cell; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, protein kinase inhibitors - imbruvica as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl). imbruvica as a single agent or in combination with rituximab or obinutuzumab or venetoclax is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. imbruvica as a single agent or in combination with bendamustine and rituximab (br) is indicated for the treatment of adult patients with cll who have received at least one prior therapy. imbruvica as a single agent is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo immunotherapy. imbruvica in combination with rituximab is indicated for the treatment of adult patients with wm.

Unió Europea - maltès - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - pomalidomide - majloma multipla - immunosoppressanti - imnovid f'kombinazzjoni ma'bortezomib u dexamethasone hu indikat fit-trattament ta'pazjenti adulti b'mjeloma multipla li rċievew mill-inqas wieħed minn qabel ta ' trattament inkluż lenalidomide. imnovid fil kombinazzjoni ma dexamethasone hija indikata fit-trattament tal-pazjenti adulti ma relapsed u refrattorji myeloma multipla li jkunu rċevew mill-inqas żewġ reġimi ta ' trattament minn qabel, inklużi kemm lenalidomide u bortezomib, u wrew progressjoni tal-marda fuq l-aħħar terapija.

Unió Europea - maltès - EMA (European Medicines Agency)

bavarian nordic a/s - vaċċin immodifikat ankara - il-virus bavarian nordic (mva-bn) - smallpox vaccine; monkeypox virus - oħra tal-vaċċini virali, - active immunisation against smallpox, monkeypox and disease caused by vaccinia virus in adults (see sections 4. 4 u 5. l-użu ta ' dan il-vaċċin għandha tkun skond ir-rakkomandazzjonijiet uffiċjali.

Unió Europea - maltès - EMA (European Medicines Agency)

techdow pharma netherlands b.v.  - enoxaparin sodium - tromboemboliżmu tal-vini - aġenti antitrombotiċi - inhixa huwa indikat għall-adulti għall -: profilassi ta ' tromboemboliżmu fil-vini, partikolarment f'pazjenti li jgħaddu minn kirurġija ortopedika, ġenerali jew onkoloġika-kirurġija. - profilassi ta 'tromboemboliżmu venuż f'pazjenti bedridden minħabba mard akut inkluż akuta insuffiċjenza tal-qalb, waqfien akut tan-nifs, infezzjonijiet gravi, kif ukoll l-aggravament tal-mard rewmatiku li jikkawżaw l-immobbilizzazzjoni tal-pazjent (japplika għall-qawwiet ta' 40 mg/0. 4 ml). trattament ta 'trombożi f' vina fonda (dvt), kkumplikati jew mhux ikkomplikati minn emboliżmu pulmonari. trattament ta 'anġina mhux stabbli u n-non-q-wave' infart mijokardijaku, flimkien ma ' acetylsalicylic acid (asa). it-trattament ta 'elevazzjoni tas-segment st' infart mijokardijaku (stemi) inklużi pazjenti li ser jiġu ttrattati b'mod konservattiv jew li wara jgħaddu minn koronarju perkutanju l-anġoplastika (japplika għall-qawwiet ta ' 60 mg/0. 6 ml, 80 mg/0. 8 ml, u 100 mg/1 ml). - tagħqid tad-demm għall-prevenzjoni fil-ċ-ċirkolazzjoni ekstrakorporali matul l-emodijalisi.