Lantus Europska Unija - malteški - EMA (European Medicines Agency)

lantus

sanofi-aventis deutschland gmbh - insulina glargine - diabetes mellitus - drogi użati fid-dijabete - trattament tad-dijabete mellitus f'adulti, adolexxenti u tfal ta 'sentejn u aktar.

Volibris Europska Unija - malteški - EMA (European Medicines Agency)

volibris

glaxosmithkline (ireland) limited - ambrisentan - pressjoni għolja, pulmonari - għal pressjoni għolja, - volibris is indicated for treatment of pulmonary arterial hypertension (pah) in adult patients of who functional class (fc) ii to iii, including use in combination treatment (see section 5.  efficacy has been shown in idiopathic pah (ipah) and in pah associated with connective tissue disease. volibris is indicated for treatment of pah in adolescents and children (aged 8 to less than 18 years) of who functional class (fc) ii to iii including use in combination treatment. efficacy has been shown in ipah, familial, corrected congenital and in pah associated with connective tissue disease (see section 5.

Ambrisentan Mylan Europska Unija - malteški - EMA (European Medicines Agency)

ambrisentan mylan

mylan s.a.s - ambrisentan - pressjoni għolja, pulmonari - għal pressjoni għolja, - ambrisentan mylan huwa indikat għall-kura tal-pressjoni għolja arterjali pulmonari (pah) f'pazjenti adulti tal-klassi funzjonali tal-who (fc) ii iii, inkluż l-użu fil-kura flimkien. l-effikaċja ntweriet f'aph idjopatika (ipah) u f'pah assoċjata ma 'mard tat-tessut konnettiv. ambrisentan mylan huwa indikat għall-kura tal-pressjoni għolja arterjali pulmonari (pah) f'pazjenti adulti tal-klassi funzjonali tal-who (fc) ii iii, inkluż l-użu fil-kura flimkien. l-effikaċja ntweriet f'aph idjopatika (ipah) u f'pah assoċjata ma 'mard tat-tessut konnettiv.

Semglee Europska Unija - malteški - EMA (European Medicines Agency)

semglee

viatris limited - insulina glargine - diabetes mellitus - drogi użati fid-dijabete - trattament tad-dijabete mellitus f'adulti, adolexxenti u tfal ta 'sentejn u aktar.

Abasaglar (previously Abasria) Europska Unija - malteški - EMA (European Medicines Agency)

abasaglar (previously abasria)

eli lilly nederland b.v. - insulina glargine - diabetes mellitus - drogi użati fid-dijabete - trattament tad-dijabete mellitus f'adulti, adolexxenti u tfal ta 'sentejn u aktar.

Hepcludex Europska Unija - malteški - EMA (European Medicines Agency)

hepcludex

gilead sciences ireland uc - bulevirtide acetate - hepatitis d, chronic - antivirali għal użu sistemiku - hepcludex is indicated for the treatment of chronic hepatitis delta virus (hdv) infection in plasma (or serum) hdv-rna positive adult patients with compensated liver disease.

Clopidogrel Teva Pharma B.V. Europska Unija - malteški - EMA (European Medicines Agency)

clopidogrel teva pharma b.v.

teva pharma b.v.  - clopidogrel (as hydrobromide) - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - aġenti antitrombotiċi - il-prevenzjoni ta aterotrombotiċi eventsclopidogrel huwa indikat f': pazjenti adulti li jbatu minn infart mijokardijaku (minn ftit jiem sa inqas minn 35 jum), puplesija iskemika (minn 7 ijiem sa inqas minn 6 xhur) jew mard arterjali periferali;f'pazjenti adulti li jsofru mis-sindromu koronarju akut: mhux elevazzjoni tas-segment st sindromu koronarju akut (anġina instabbli jew mhux-mewġa-q infart mijokardijaku), li jinkludu pazjenti fi proċess li titpoġġa stent wara intervent koronarju perkutanju, flimkien ma ' acetylsalicylic acid (asa);elevazzjoni tas-segment st infart mijokardijaku akut, flimkien ma ' asa f'medikament pazjenti kkurati b'eliġibbli għat-terapija trombolitika. il-prevenzjoni ta aterotrombotiċi u avvenimenti tromboemboliċi fil-fibrillazzjoni ta 'l-fibrillationin pazjenti adulti li jbatu minn fibrillazzjoni atrijali li jkollhom mill-inqas fattur ta' riskju wieħed għall-episodji vaskulari, mhumiex adattati għall-kura bil-vitamina k antagonisti (vka) u li għandhom baxx-riskju ta'fsada, clopidogrel huwa indikat, flimkien ma ' asa għall-prevenzjoni tal-aterotrombotiċi u avvenimenti tromboemboliċi, inkluż puplesija.

Olanzapine Glenmark Europe Europska Unija - malteški - EMA (European Medicines Agency)

olanzapine glenmark europe

glenmark arzneimittel gmbh - olanzapine - schizophrenia; bipolar disorder - psikolettiċi - adultsolanzapine huwa indikat għall-kura ta ' skizofrenja. olanzapine hija effettiva biex iżżomm it-titjib kliniku waqt terapija kontinwa f'pazjenti li wrew rispons inizjali għat-trattament. olanzapine hu indikat għall-kura moderata għal severa ta ' episodju ta'manija. f'pazjenti li l-episodju ta'manija għandu rrispondew għat-trattament b'olanzapine, olanzapine hija indikata għall-prevenzjoni ta'rikorrenza f'pazjenti b'diżordni bipolari.

Pioglitazone Teva Pharma Europska Unija - malteški - EMA (European Medicines Agency)

pioglitazone teva pharma

teva pharma b.v. - pioglitazone hydrochloride - diabetes mellitus, tip 2 - drogi użati fid-dijabete - pioglitazone is indicated in the treatment of type-2 diabetes mellitus as monotherapy: , in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance. , pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance. wara l-bidu tat-terapija b'pioglitazone, il-pazjenti għandhom jiġu riveduti wara 3 sa 6 xhur biex tevalwa l-adegwatezza tal-rispons għall-kura (e. it-tnaqqis fl-hba1c). f'pazjenti li jonqsu li juru rispons adegwat, pioglitazone għandu jitwaqqaf. fid-dawl tar-riskji potenzjali fit-tul mal-terapija, it-tobba għandhom jikkonfermaw fil-sussegwenti ta 'rutina reviżjonijiet li l-benefiċċju ta' pioglitazone jinżamm.

Clopidogrel Taw Pharma (previously Clopidogrel Mylan) Europska Unija - malteški - EMA (European Medicines Agency)

clopidogrel taw pharma (previously clopidogrel mylan)

taw pharma (ireland) limited - clopidogrel hydrochloride - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - aġenti antitrombotiċi - , , , , secondary prevention of atherothrombotic events, , clopidogrel is indicated in: , - adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. , - adult patients suffering from acute coronary syndrome:,    - non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). ,     - st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is), clopidogrel in combination with asa is indicated in:, - adult patients with moderate to high-risk tia (abcd2  score ≥4) or minor is (nihss  ≤3) within 24 hours of either the tia or is event.  , , prevention of atherothrombotic and thromboembolic events in atrial fibrillation, in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. , , for further information please refer to section 5. , , ,.