Voriconazole Hikma (previously Voriconazole Hospira) ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

voriconazole hikma (previously voriconazole hospira)

hikma farmaceutica (portugal) s.a. - voriconazolo - bacterial infections and mycoses; aspergillosis; candidiasis - antimicotici per uso sistemico - voriconazolo è un ampio spettro, triazolo agente antimicotico ed è indicato negli adulti e nei bambini di età compresa tra 2 anni e sopra come segue:il trattamento dell'aspergillosi invasiva;trattamento di candidaemia non neutropenici pazienti;trattamento di fluconazole-resistant gravi infezioni da candida invasive (tra cui c. krusei);il trattamento di gravi infezioni fungine causate da scedosporium spp. e fusarium spp.. voriconazolo deve essere somministrato principalmente a pazienti con progressiva, possibilmente infezioni life-threatening. profilassi di infezioni fungine invasive ad alto rischio allogenico di cellule staminali emopoietiche (hsct)destinatari.

Vfend ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

vfend

pfizer europe ma eeig - voriconazolo - candidiasis; mycoses; aspergillosis - antimicotici per uso sistemico - voriconazolo, è un ampio spettro, triazolo agente antimicotico ed è indicato negli adulti e nei bambini di età compresa tra 2 anni e sopra come segue:il trattamento dell'aspergillosi invasiva;trattamento di candidaemianon-pazienti neutropenici;trattamento di fluconazole-resistant gravi infezioni da candida invasive (tra cui c. krusei);il trattamento di gravi infezioni fungine causate da scedosporium spp. e fusarium spp.. vfend deve essere somministrato principalmente a pazienti con progressiva, possibilmente infezioni life-threatening. profilassi di infezioni fungine invasive ad alto rischio allogenico di cellule staminali emopoietiche (hsct) destinatari.

Voriconazole Accord ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

voriconazole accord

accord healthcare s.l.u. - voriconazolo - aspergillosis; candidiasis; mycoses - antimicotici per uso sistemico, derivati triazolo - voriconazolo è un ampio spettro, triazolo agente antimicotico ed è indicato negli adulti e nei bambini dai due anni e sopra come segue:il trattamento dell'aspergillosi invasiva;trattamento di candidaemia non neutropenici pazienti;trattamento di fluconazole-resistant gravi infezioni da candida invasive (tra cui c. krusei);il trattamento di gravi infezioni fungine causate da scedosporium spp. e fusarium spp.. voriconazolo accord deve essere somministrato principalmente a pazienti con progressiva, possibilmente infezioni life-threatening.

Pacifica Xpert ইতালী - ইতালীয় - Ministero della Salute

pacifica xpert

bayer ag - iodosulfuron metil sodio; amidosulfuron; mefenpyr etere; mesosulfuron-metile; - granuli idrodispersibili - 1.0 g; 5.0 g; 9.0 g; 3.0 g i valori indicati sono per 100 g di prodotto. - mesosulfuron-methyl; 3%; iodosulfuron-methyl; sodium; 1%; amidosulfuron; 5% - diserbante

Decis Evo ইতালী - ইতালীয় - Ministero della Salute

decis evo

bayer ag - deltametrina; - emulsione olio in acqua - 2.42 g i valori indicati sono per 100 g di prodotto. - deltametrina; 2,42%; (25; g/l) - insetticida

Ketek ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

ketek

aventis pharma s.a. - telitromicina - sinusitis; tonsillitis; bronchitis, chronic; pharyngitis; community-acquired infections; pneumonia, bacterial - antibatterici per uso sistemico, - quando si prescrive ketek, si dovrebbe prendere in considerazione una guida ufficiale sull'uso appropriato degli agenti antibatterici e sulla prevalenza locale della resistenza. ketek è indicato per il trattamento delle seguenti infezioni:in pazienti di 18 anni e oldercommunity polmonite acquisita in, lieve o moderata. quando il trattamento di infezioni causate da noti o sospetti beta-lattamici e / o macrolidi-ceppi resistenti (secondo la storia di pazienti e / o nazionali e / o regionali resistenza di dati coperti dal antibatterico spettro di telitromicina:esacerbazione acuta di bronchite cronica;sinusite acuta;in pazienti di 12 anni e oldertonsillitis / faringite causata da streptococcus pyogenes, come alternativa quando antibiotici beta-lattamici non sono appropriati in paesi / regioni con una significativa prevalenza di macrolidi-resistente s. pyogenes, quando mediata da ermtr o mefa.

Keytruda ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

keytruda

merck sharp & dohme b.v. - pembrolizumab - melanoma; hodgkin disease; carcinoma, renal cell; carcinoma, non-small-cell lung; carcinoma, transitional cell; squamous cell carcinoma of head and neck; urologic neoplasms; endometrial neoplasms - agenti antineoplastici - melanomakeytruda as monotherapy is indicated for the treatment of adults and adolescents aged 12 years and older with advanced (unresectable or metastatic) melanoma. keytruda as monotherapy is indicated for the adjuvant treatment of adults and adolescents aged 12 years and older with stage iib, iic, or with stage iii melanoma and lymph node involvement who have undergone complete resection. non small cell lung carcinoma (nsclc)keytruda as monotherapy is indicated for the adjuvant treatment of adults with non-small cell lung carcinoma who are at high risk of recurrence following complete resection and platinum based chemotherapy (for selection criteria, see section 5. keytruda as monotherapy is indicated for the first line treatment of metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 50% tumour proportion score (tps) with no egfr or alk positive tumour mutations. keytruda, in combination with pemetrexed and platinum chemotherapy, is indicated for the first-line treatment of metastatic non squamous non small cell lung carcinoma in adults whose tumours have no egfr or alk positive mutations. keytruda, in combination with carboplatin and either paclitaxel or nab paclitaxel, is indicated for the first line treatment of metastatic squamous non small cell lung carcinoma in adults. keytruda  as monotherapy is indicated for the treatment of locally advanced or metastatic non small cell lung carcinoma in adults whose tumours express pd l1 with a ≥ 1% tps and who have received at least one prior chemotherapy regimen. i pazienti con egfr o alk positivo mutazioni tumorali devono, inoltre, hanno ricevuto la terapia mirata prima di ricevere keytruda. classical hodgkin lymphoma (chl)keytruda as monotherapy is indicated for the treatment of adult and paediatric patients aged 3 years and older with relapsed or refractory classical hodgkin lymphoma who have failed autologous stem cell transplant (asct) or following at least two prior therapies when asct is not a treatment option. urothelial carcinomakeytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who have received prior platinum containing chemotherapy. keytruda as monotherapy is indicated for the treatment of locally advanced or metastatic urothelial carcinoma in adults who are not eligible for cisplatin containing chemotherapy and whose tumours express pd l1 with a combined positive score (cps) ≥ 10. head and neck squamous cell carcinoma (hnscc)keytruda, as monotherapy or in combination with platinum and 5 fluorouracil (5 fu) chemotherapy, is indicated for the first line treatment of metastatic or unresectable recurrent head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a cps ≥ 1. keytruda as monotherapy is indicated for the treatment of recurrent or metastatic head and neck squamous cell carcinoma in adults whose tumours express pd l1 with a ≥ 50% tps and progressing on or after platinum containing chemotherapy. renal cell carcinoma (rcc)keytruda, in combination with axitinib, is indicated for the first line treatment of advanced renal cell carcinoma in adults. keytruda  as monotherapy is indicated for the adjuvant treatment of adults with renal cell carcinoma at increased risk of recurrence following nephrectomy, or following nephrectomy and resection of metastatic lesions (for selection criteria, please see section 5. microsatellite instability high (msi-h) or mismatch repair deficient (dmmr) cancerscolorectal cancer (crc)keytruda as monotherapy is indicated for theadults with msi-h or dmmr colorectal cancer in the following settings:first line treatment of metastatic microsatellite instability high (msi h) or mismatch repair deficient (dmmr) colorectal cancer in adults;treatment of unresectable or metastatic colorectal cancer after previous fluoropyrimidine based combination therapy.  non-colorectal cancerskeytruda as monotherapy is indicated for the treatment of the following msi h or dmmr tumours in adults with:advanced or recurrent endometrial carcinoma, who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation;unresectable or metastatic gastric, small intestine, or biliary cancer, who have disease progression on or following at least one prior therapy. oesophageal carcinomakeytruda, in combination with platinum and fluoropyrimidine based chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic carcinoma of the oesophagus or her-2 negative gastroesophageal junction adenocarcinoma, in adults whose tumours express pd l1 with a cps ≥ 10. triple negative breast cancer (tnbc)keytruda, in combination with chemotherapy as neoadjuvant treatment, and then continued as monotherapy as adjuvant treatment after surgery, is indicated for the treatment of adults with locally advanced, or early stage triple negative breast cancer at high risk of recurrence. keytruda, in combination with chemotherapy, is indicated for the treatment of locally recurrent unresectable or metastatic triple negative breast cancer in adults whose tumours express pd l1 with a cps ≥ 10 and who have not received prior chemotherapy for metastatic disease. endometrial carcinoma (ec)keytruda, in combination with lenvatinib, is indicated for the treatment of advanced or recurrent endometrial carcinoma in adults who have disease progression on or following prior treatment with a platinum containing therapy in any setting and who are not candidates for curative surgery or radiation. cervical cancerkeytruda, in combination with chemotherapy with or without bevacizumab, is indicated for the treatment of persistent, recurrent, or metastatic cervical cancer in adults whose tumours express pd l1 with a cps ≥ 1. gastric or gastro-oesophageal junction (gej) adenocarcinomakeytruda, in combination with trastuzumab, fluoropyrimidine and platinum-containing chemotherapy, is indicated for the first-line treatment of locally advanced unresectable or metastatic her2-positive gastric or gastro-oesophageal junction adenocarcinoma in adults whose tumours express pd-l1 with a cps ≥ 1.

Levviax ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

levviax

aventis pharma s.a. - telitromicina - community-acquired infections; pharyngitis; bronchitis, chronic; pneumonia; tonsillitis; sinusitis - antibatterici per uso sistemico, - quando si prescrive levviax, si deve prendere in considerazione una guida ufficiale sull'uso appropriato degli agenti antibatterici e sulla prevalenza locale della resistenza (vedere anche le sezioni 4).. 4 e 5. levviax è indicato per il trattamento delle seguenti infezioni:in pazienti di età superiore a 18 anni:-polmonite acquisita in comunità, di lieve o moderata (vedere paragrafo 4. - durante il trattamento di infezioni causate da noti o sospetti beta-lattamici e/o macrolidi ceppi resistenti (secondo la storia di pazienti e / o nazionali e/o regionali resistenza di dati coperti dal antibatterico spettro di telitromicina (vedere sezioni 4. 4 e 5. 1):- esacerbazione acuta di bronchite cronica, acuta sinusitisin pazienti di 12 anni ed oltre:- tonsillite/faringite causata da streptococcus pyogenes, come alternativa quando beta lattamici non sono appropriati in paesi/regioni con una significativa prevalenza di macrolide resistant s. pyogenes, quando mediato da ermtr o mefa (vedere paragrafi 4). 4 e 5.

Scintimun ইউরোপীয় ইউনিয়ন - ইতালীয় - EMA (European Medicines Agency)

scintimun

cis bio international  - besilesomab - osteomyelitis; radionuclide imaging - radiofarmaci diagnostici - questo medicinale è solo per uso diagnostico e l'indicazione approvata è l'imaging scintigrafico, in combinazione con altre modalità di imaging appropriate, per determinare la posizione dell'infiammazione / infezione nell'osso periferico negli adulti con sospetta osteomielite. scintimun non deve essere usato per la diagnosi di infezione del piede diabetico.