Byannli (previously Paliperidone Janssen-Cilag International) Unjoni Ewropea - Malti - EMA (European Medicines Agency)

byannli (previously paliperidone janssen-cilag international)

janssen-cilag international n.v.   - palmpalidone palmitate - skizofrenija - psikolettiċi - byannli (previously paliperidone janssen-cilag international) a 6 monthly injection, is indicated for the maintenance treatment of schizophrenia in adult patients who are clinically stable on 1 monthly or 3 monthly paliperidone palmitate injectable products (see section 5.

Invokana Unjoni Ewropea - Malti - EMA (European Medicines Agency)

invokana

janssen-cilag international nv - canagliflozin - diabetes mellitus, tip 2 - drogi użati fid-dijabete - invokana is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise:as monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. 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.

Vokanamet Unjoni Ewropea - Malti - EMA (European Medicines Agency)

vokanamet

janssen-cilag international nv - canagliflozin, metformin hydrochloride - diabetes mellitus, tip 2 - drogi użati fid-dijabete - vokanamet huwa indikat f'adulti ta '18-il sena u akbar b'dijabete mellitus tip 2 bħala żieda mad-dieta u l-eżerċizzju biex itejjeb il-kontroll gliċemiku:f'pazjenti li mhumiex kontrollati sew fuq xieraq bl-felħu dożi ta' metformin alonein pazjenti fuq xieraq bl-felħu dożi ta 'metformin flimkien ma' oħrajn li jbaxxu glucose-prodotti mediċinali inkluża l-insulina, meta dawn ma jipprovdux kontroll gliċemiku adegwat. fil-pazjenti li diġà qegħdin jiġu kkurati b'kumbinazzjoni ta canagliflozin u metformin bħala separati tabletsfor-riżultati tal-istudju fir-rigward tal-kombinazzjoni ta ' terapiji, l-effetti fuq il-kontroll gliċemiku u episodji kardjovaskulari, u l-popolazzjonijiet studjati, ara sezzjonijiet 4. 4, 4. 5 u 5.

Natpar Unjoni Ewropea - Malti - EMA (European Medicines Agency)

natpar

takeda pharmaceuticals international ag ireland branch - ormon tal-paratirojde - ipoparatirojdiżmu - homeostasi tal-kalċju - natpar huwa indikat bħala trattament aġġuntiv ta 'pazjenti adulti b'ipoparatirojdiżmu kroniku li ma jistgħux jiġu kkontrollati b'mod adegwat b'terapija standard waħidha.

Upstaza Unjoni Ewropea - Malti - EMA (European Medicines Agency)

upstaza

ptc therapeutics international limited - eladocagene exuparvovec - amino acid metaboliżmu, Żbalji inborn - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.

Ponvory Unjoni Ewropea - Malti - EMA (European Medicines Agency)

ponvory

janssen-cilag international n.v.    - ponesimod - l-isklerożi multipla, sklerożi multipla li tirkadi u tbatti - immunosoppressanti - ponvory is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Segluromet Unjoni Ewropea - Malti - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - diabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Spedra Unjoni Ewropea - Malti - EMA (European Medicines Agency)

spedra

menarini international operations luxembourg s.a. - avanafil - disfunzjoni erettili - drogi użati f'każ ta 'disfunzjoni erettili - trattament ta 'disfunzjoni erettili f'irġiel adulti. sabiex spedra ikun effettiv, hija meħtieġa stimulazzjoni sesswali.

Zytiga Unjoni Ewropea - Malti - EMA (European Medicines Agency)

zytiga

janssen-cilag international n.v. - abiraterone acetate - neoplasmi prostatiċi - terapija endokrinali - zytiga huwa indikat ma 'prednisone jew prednisolone: - trattament tal-kanċer metastatiku tal-kastrazzjoni reżistenti għall-kanċer tal-prostata fl-irġiel adulti li huma asintomatiċi jew ħafif sintomatika wara l-falliment tat-terapija tal-privazzjoni tal-androgen fil-għalihom kimoterapija għadu mhux klinikament indicatedthe-trattament tal-kanċer metastatiku tal-kastrazzjoni reżistenti għall-kanċer tal-prostata fl-irġiel adulti li l-marda tagħhom mexa fuq jew wara docetaxel kimoterapija bbażata fuq il-kors ta'.

Bravecto Plus Unjoni Ewropea - Malti - EMA (European Medicines Agency)

bravecto plus

intervet international b.v. - fluralaner, moksidektin - antiparasitic products, insecticides and repellents, endectocides, milbemycins - qtates - għall-qtates b', jew huma f'riskju minn mħallta ' infestazzjonijiet parassitiċi mill-qurdien jew ma l-briegħed u l-dud tal-widnejn, gastro-nematodi jew dudu tal-qalb. il-prodott mediċinali veterinarju huwa esklussivament indikat meta l-użu kontra l-briegħed u l-qurdien jew waħda jew iżjed ta'l-oħra fil-mira parassiti huwa indikat fl-istess ħin. għat-trattament ta ' qurdien u infestazzjonijiet mill-briegħed fil-qtates li jipprovdu immedjata u persistenti tal-briegħed (ctenocephalides felis) u qurdien (ixodes ricinus) qtil attività għal 12-il ġimgħa. il-briegħed u l-qurdien għandhom jingħaqdu ma 'l-ospitant u jibdew jgħumu sabiex ikunu esposti għas-sustanza attiva. il-prodott jista 'jintuża bħala parti minn strateġija ta' trattament għal dermatite tal-allerġija tal-briegħed (fad). għat-trattament ta ' infestazzjonijiet bil-dud tal-widnejn (otodectes cynotis). għall-kura ta ' infezzjonijiet bl-intestinali minn infezzjonijiet mill-ħniex (4-istadju tal-larva, adulti immaturi u l-adulti tal-toxocara cati) u għall (4-istadju tal-larva, adulti immaturi u l-adulti tal-ancylostoma tubaeforme). meta jingħata ripetutament fi 12-il-ġimgħa l-intervall, il-prodott kontinwament tipprevjeni l-mard tal-heartworm ikkawżata mid-dirofilaria immitis.