Unione Europea - italiano - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - cedazuridine, decitabine - leucemia, mieloide - agenti antineoplastici - inaqovi is indicated as monotherapy for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (aml) who are ineligible for standard induction chemotherapy.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

kedrion s.p.a. - immunoglobuline, umane normali, per somm. extravascolare - immunoglobuline, umane normali, per somm. extravascolare

Unione Europea - italiano - EMA (European Medicines Agency)

samsung bioepis nl b.v. - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - agenti antineoplastici - aybintio in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. aybintio in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. per ulteriori informazioni sullo stato del recettore del fattore di crescita epidermico umano 2 (her2), fare riferimento alla sezione 5. 1 of the smpc. aybintio in combination with capecitabine is indicated for first-line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracyclinecontaining regimens in the adjuvant setting within the last 12 months should be excluded from treatment with aybintio in combination with capecitabine. per ulteriori informazioni sullo stato her2, fare riferimento alla sezione 5. 1 of the smpc. aybintio, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. aybintio, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. 1 of the smpc). aybintio in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. aybintio, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. 1 of the smpc). aybintio, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents. aybintio, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum-resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. 1 of the smpc). aybintio, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5. 1 of the smpc).

Unione Europea - italiano - EMA (European Medicines Agency)

centus biotherapeutics europe limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell - agenti antineoplastici - bevacizumab in combinazione con chemioterapia a base di fluoropirimidina è indicato per il trattamento di pazienti adulti con carcinoma metastatico del colon o del retto. bevacizumab in combinazione con paclitaxel è indicato per il trattamento di prima linea di pazienti adulti con carcinoma mammario metastatico. per ulteriori informazioni sullo stato del recettore del fattore di crescita epidermico umano 2 (her2), fare riferimento alla sezione 5. bevacizumab in combinazione con capecitabina è indicato per il trattamento di prima linea di pazienti adulti con carcinoma mammario metastatico nei quali il trattamento con chemioterapia opzioni, tra cui i taxani o antracicline non è considerato appropriato. patients who have received taxane and anthracycline- containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with equidacent in combination with capecitabine. per ulteriori informazioni sullo stato her2, fare riferimento alla sezione 5. bevacizumab, in addition to platinum-based chemotherapy, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-small cell lung cancer other than predominantly squamous cell histology. bevacizumab, in combinazione con erlotinib, è indicato per il trattamento di prima linea di pazienti adulti con metastasi avanzato, metastatico o ricorrente non squamose del polmone non a piccole cellule cancro con epidermal growth factor receptor (egfr) mutazioni attivanti. bevacizumab in combination with interferon alfa-2a is indicated for first-line treatment of adult patients with advanced and/or metastatic renal cell cancer. bevacizumab, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iiib, iiic and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. bevacizumab, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum-sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor-targeted agents. bevacizumab, in combinazione con paclitaxel e cisplatino o, in alternativa, paclitaxel e topotecan in pazienti che non possono ricevere platino terapia, è indicato per il trattamento di pazienti adulti con persistente, ricorrente o metastatico carcinoma della cervice uterina.

Unione Europea - italiano - EMA (European Medicines Agency)

ipsen pharma - cabozantinib (s)-malate - carcinoma, renal cell; carcinomas, hepatocellular - agenti antineoplastici - renal cell carcinoma (rcc)cabometyx is indicated as monotherapy for the treatment of advanced renal cell carcinoma (rcc):in treatment-naïve adults with intermediate or poor risk,in adults following prior vascular endothelial growth factor (vegf)-targeted therapy. cabometyx, in combination with nivolumab, is indicated for the first-line treatment of advanced renal cell carcinoma in adults. hepatocellular carcinoma (hcc)cabometyx is indicated as monotherapy for the treatment of hepatocellular carcinoma (hcc) in adults who have previously been treated with sorafenib.

Unione Europea - italiano - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - immunosoppressori selettivi - la colite colitisentyvio è indicato per il trattamento di pazienti adulti con moderatamente a gravemente attiva la colite ulcerosa, che hanno avuto una risposta inadeguata, persa la risposta, o sono intolleranti a terapia convenzionale o fattore di necrosi tumorale alfa (tnfa) antagonista. il morbo di crohn diseaseentyvio è indicato per il trattamento di pazienti adulti con moderata a grave malattia di crohn attiva che hanno avuto una risposta inadeguata, persa la risposta, o sono intolleranti a terapia convenzionale o fattore di necrosi tumorale alfa (tnfa) antagonista. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Unione Europea - italiano - EMA (European Medicines Agency)

baxalta innovations gmbh - vonicog alfa - malattie di von willebrand - antiemorragici - veyvondi è indicato negli adulti (età 18 anni) con malattia di von willebrand (vwd), quando la desmopressina (ddavp) al solo trattamento è inefficace o non è indicato per il trattamento di emorragie e sanguinamento chirurgico per la prevenzione del sanguinamento chirurgico. veyvondi non deve essere usato nel trattamento dell'emofilia a.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

biotest pharma gmbh - immunoglobuline, umane normali, per somm. intravascolare - immunoglobuline, umane normali, per somm. intravascolare

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

octapharma ag - immunoglobulinum humanum normale - soluzione iniettabile - immunoglobulinum humanum normale 165 mg, maltosum, polysorbatum 80, aqua ad iniectabile, ad solutionem pro 1 ml. - substitutionstherapie bei erwachsenen, kindern und jugendlichen (0 18 jahre) bei ; - primären immunmangelkrankheiten (pid) mit eingeschränkter antikörperbildung. ; - sekundären immunmangelkrankheiten (sid) bei patienten, die an schweren oder rezidivierenden infektionen leiden, bei denen eine antimikrobielle therapie ; unwirksam ist und die entweder ein nachgewiesenes versagen spezifischer antikörper (psaf)* oder igg-serum-spiegel von <4g/l aufweisen.; *psaf = nichterreichen eines mindestens zweifachen anstiegs des igg-antikörpertiters für impfstoffe mit pneumokokken-polysacchariden und polypeptid- ; antigenen. - emoderivati

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

baxalta innovations gmbh - immunoglobuline, umane normali, per somm. intravascolare - immunoglobuline, umane normali, per somm. intravascolare