Phelinun Europeiska unionen - litauiska - EMA (European Medicines Agency)

phelinun

adienne s.r.l. s.u. - melphalan hydrochloride - multiple myeloma; hodgkin disease; lymphoma, non-hodgkin; precursor cell lymphoblastic leukemia-lymphoma; leukemia, myeloid, acute; neuroblastoma; ovarian neoplasms; hematopoietic stem cell transplantation - antinavikiniai vaistai - high-dose of phelinun used alone or in combination with other cytotoxic medicinal products and/or total body irradiation is indicated in the treatment of:multiple myeloma,malignant lymphoma (hodgkin, non-hodgkin lymphoma),acute lymphoblastic and myeloblastic leukemia,childhood neuroblastoma,ovarian cancer,mammary adenocarcinoma. phelinun in combination with other cytotoxic medicinal products is indicated as reduced intensity conditioning (ric) treatment prior to allogeneic haematopoietic stem cell transplantation (allo-hsct) in malignant haematological diseases in adults. phelinun in combination with other cytotoxic medicinal products is indicated as conditioning regimen prior to allogeneic haematopoietic stem cell transplantation in haematological diseases in the paediatric population as:myeloablative conditioning (mac) treatment in case of malignant haematological diseasesric treatment in case of non-malignant haematological diseases.

Pepaxti Europeiska unionen - litauiska - EMA (European Medicines Agency)

pepaxti

oncopeptides ab - melphalan flufenamide hydrochloride - daugybinė mieloma - antinavikiniai vaistai - pepaxti is indicated, in combination with dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least three prior lines of therapies, whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and one anti-cd38 monoclonal antibody, and who have demonstrated disease progression on or after the last therapy. for patients with a prior autologous stem cell transplantation, the time to progression should be at least 3 years from transplantation (see section 4.

LORINDEN A Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

lorinden a

bausch health ireland limited - flumetazonas/salicilo rūgštis - tepalas - 0,2 mg/30 mg/g - flumetasone

FLUCINAR N Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

flucinar n

bausch health ireland limited - fluocinolono acetonidas/neomicino sulfatas - tepalas - 0,25 mg/5 mg/g - fluocinolone acetonide and antibiotics

OXYCORT Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

oxycort

bausch health ireland limited - oksitetraciklinas/hidrokortizonas - tepalas - 30 mg/10 mg/g - hydrocortisone and antibiotics

FLUCINAR Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

flucinar

bausch health ireland limited - fluocinolono acetonidas - gelis - 0,25 mg/g - fluocinolone acetonide

Betnovate Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

betnovate

glaxosmithkline trading services limited - betametazonas - odos emulsija - 1 mg/g - betamethasone

Opatanol Europeiska unionen - litauiska - EMA (European Medicines Agency)

opatanol

novartis europharm limited - olopatadino hidrochloridas - konjunktyvitas, alerginis - oftalmologai - akių požymiai ir simptomai sezoninio alerginio konjunktyvito gydymas.

Zovirax Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

zovirax

glaxosmithkline dungarvan limited - acikloviras - kremas - 50 mg/g - aciclovir

Vizitrav Litauen - litauiska - SMCA (Valstybinė vaistų kontrolės tarnyba)

vizitrav

bausch + lomb ireland limited - travoprostas - akių lašai (tirpalas) - 40 µg/ml - travoprost