Unjoni Ewropea - Malti - EMA (European Medicines Agency)

takeda pharma a/s - ixazomib citrate - majloma multipla - aġenti antineoplastiċi - ninlaro flimkien ma ' lenalidomide u dexamethasone huwa indikat għall-kura tal-pazjenti adulti bil-myeloma multipla li rċevew terapija għall-inqas wieħed minn qabel.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi winthrop industrie - clopidogrel hydrogen sulfate - stroke; peripheral vascular diseases; atrial fibrillation; myocardial infarction; acute coronary syndrome - aġenti antitrombotiċi - secondary prevention of atherothrombotic eventsclopidogrel is indicated in:adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from seven days until less than six 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 patients undergoing percutaneous coronary intervention (including patients undergoing a stent replacement) or medically treated patients eligible for thrombolytic/fibrinolytic therapy. in patients with moderate to high-risk transient ischemic attack (tia) or minor ischemic 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. 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 u li għandhom baxx-riskju ta'fsada, clopidogrel huwa indikat, flimkien ma ' asa għall-prevenzjoni tal-aterotrombotiċi u avvenimenti tromboemboliċi, inkluż puplesija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sonidegib difosfat - karċinoma, Ċellula basal - aġenti antineoplastiċi - odomzo huwa indikat għat-trattament ta 'pazjenti adulti b'karċinoma taċ-ċelluli bażali lokalment avvanzati (bcc) li mhumiex suġġetti għal kirurġija ta' kura jew terapija bir-radjazzjoni.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - thalidomide - majloma multipla - immunosoppressanti - thalidomide bms in combination with melphalan and prednisone as first line treatment of patients with untreated multiple myeloma, aged >/= 65 years or ineligible for high dose chemotherapy. thalidomide bms is prescribed and dispensed according to the thalidomide celgene pregnancy prevention programme (see section 4.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

norton healthcare ltd. - paclitaxel - sarcoma, kaposi; carcinoma, non-small-cell lung; ovarian neoplasms; breast neoplasms - aġenti antineoplastiċi - paxene huwa indikat għall-kura ta 'pazjenti b':• avvanzati relatat mal-aids sarkoma ta'kaposi (aids-ks) li ma rnexxewx qabel anthracycline liposomali-terapija;• karċinoma metastatika ta'l-sider (mbc) li ma jkunux ħadmu jew ma jkunux-kandidati għall-istandard anthracycline-terapija li jkun fiha;• karċinoma avvanzata ta 'l-ovarji (aoc) jew bi residwu tal-marda (> 1 ċm) wara l-ewwel laparotomija, flimkien ma' cisplatin bħala l-ewwel linja ta 'trattament;• karċinoma metastatika ta' l-ovarju (moc) wara l-falliment ta jkun fihom il-platinu terapija kombinata mingħajr taxanes bħala t-tieni linja ta 'trattament;• non-small cell lung avvanzata (nsclc) li mhumiex kandidati għall-potenzjalment kurattiva-kirurġija u/jew terapija ta' radjazzjoni, flimkien ma ' cisplatin. dejta ta 'effikaċja limitata tappoġġja din l-indikazzjoni (ara sezzjoni 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pfizer europe ma eeig - pemetrexed ditromethamine - carcinoma, non-small-cell lung; mesothelioma - l-aċidu foliku l-analogi tagħhom, antimetaboliti - plewrali malinna mesotheliomapemetrexed hospira uk limited flimkien ma ' cisplatin huwa indikat għat-trattament tal-kimoterapija naïve pazjenti b'mesoteljoma plewrali malinna u li ma jistax jitneħħa. taċ-ċelluli mhux żgħar tal-pulmun cancerpemetrexed hospira uk limited flimkien ma 'cisplatin huwa indikat għall-kura tal-ewwel linja ta' pazjenti b'lokalment avvanzat jew metastatiku taċ-ċelluli mhux żgħar tal-pulmun il-kanċer l-oħra mill-aktar istoloġija taċ-ċellola skwamuża (ara l-smpc taqsima 5. pemetrexed hospira uk limited huwa indikat bħala monoterapija għall-kura ta 'manteniment ta lokalment avvanzat jew metastatiku taċ-ċelluli mhux żgħar tal-pulmun il-kanċer l-oħra mill-aktar istoloġija ta' ċelluli skwamużi fir-pazjenti li l-marda tagħhom ma jkunx hemm progress immedjatament wara ibbażat fuq il-platinu ' kimoterapija (ara l-smpc taqsima 5. pemetrexed hospira uk limited huwa indikat bħala monoterapija għall-tieni linja ta 'trattament ta' pazjenti b'lokalment avvanzat jew metastatiku taċ-ċelluli mhux żgħar tal-pulmun il-kanċer l-oħra mill-aktar istoloġija taċ-ċellola skwamuża (ara l-smpc taqsima 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

krka, d.d., novo mesto - clopidogrel (as hydrogen sulfate) - peripheral vascular diseases; stroke; acute coronary syndrome; myocardial infarction - aġenti antitrombotiċi - - prevenzjoni sekondarja prevenzjoni ta ' avvenimenti aterotrombotiċi clopidogrel huwa indikat fl: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. pazjenti adulti li jsofru mis-sindromu koronarju akut:- nuqqas ta 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). l - 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 atrijali:- fil-pazjenti adulti li jbatu minn fibrillazzjoni atrijali li jkollhom mill-inqas fattur ta 'riskju wieħed għall-episodji vaskulari, mhumiex adattati għall-kura bl-antagonisti tal-vitamina k (vka) u li għandhom baxx-riskju ta'fsada, clopidogrel huwa indikat, flimkien ma' asa għall-prevenzjoni tal-aterotrombotiċi u avvenimenti tromboemboliċi, inkluż puplesija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

advanced accelerator applications - lutetium (177lu) oxodotreotide - tumuri newroentokrini - radjufarmaċewtiċi terapewtiċi oħra - lutathera huwa indikat għat-trattament ta ' unresectable jew metastatic, b'mod progressiv, ukoll differenzjati (g1 u g2), somatostatin r-riċevitur gastroenteropancreatic pożittiv neuroendocrine tumuri (gep‑nets) fl-adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pierre fabre medicament - encorafenib - melanoma; colorectal neoplasms - aġenti antineoplastiċi - encorafenib is indicated:in combination with binimetinib is indicated for the treatment of adult patients with unresectable or metastatic melanoma with a braf v600 mutationin combination with cetuximab, for the treatment of adult patients with metastatic colorectal cancer (crc) with a braf v600e mutation, who have received prior systemic therapy.

Unjoni Ewropea - Malti - 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.