União Europeia - lituano - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - tolvaptan - netinkamas adh sindromas - diuretikai, - suaugusių pacientų, sergančių netinkamą antidiurezinio hormono sekreciją (siadh), sindromu pasireiškusios hiponatremijos gydymas..

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

zakłady farmaceutyczne polpharma s.a. - furozemidas - injekcinis tirpalas - 20 mg/2 ml - furosemide

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

pharmaceutical works polpharma s.a. - furozemidas - tabletės - 40 mg - furosemide

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

as kalceks - furozemidas - injekcinis ar infuzinis tirpalas - 10 mg/ml - furosemide

União Europeia - lituano - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - bevacizumabas - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antinavikiniai vaistai - vegzelma in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. vegzelma in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. daugiau informacijos apie žmogaus epidermio augimo faktoriaus receptorių 2 (her2) būklę rasite 5 skyriuje. vegzelma 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 anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with vegzelma in combination with capecitabine. daugiau informacijos apie her2 statusą rasite 5 skyriuje. vegzelma, 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 (nsclc) other than predominantly squamous cell histology. vegzelma, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent nsclc with epidermal growth factor receptor (egfr) activating mutations (see section 5. vegzelma, in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. vegzelma, 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. vegzelma, 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 vascular endothelial growth factor (vegf) inhibitors or vegf receptor–targeted agents. vegzelma in combination with paclitaxel, 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. vegzelma, 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.

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

pharmaceutical works polpharma s.a. - acetazolamidas - tabletės - 250 mg - acetazolamide

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

menarini international operations luxembourg s.a. - torazemidas - tabletės - 20 mg/4 ml; 200 mg; 10 mg - torasemide

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

ferring gmbh - desmopresinas - geriamasis liofilizatas - 50 µg; 25 µg - desmopressin

Lituânia - lituano - SMCA (Valstybinė vaistų kontrolės tarnyba)

fresenius kabi polska sp.z.o.o. - gliukozė - infuzinis tirpalas - 200 mg/ml; 50 g/1000 ml; 100 g/1000 ml - carbohydrates

União Europeia - lituano - EMA (European Medicines Agency)

dompé biotec s.p.a. - darbepoetinas alfa - kidney failure, chronic; anemia; cancer - antianeminiai preparatai - simptominės anemijos, susijusios su lėtiniu inkstų nepakankamumu (crf), gydymas suaugusiems ir vaikams. gydymas simptominis anemija suaugusiųjų sergančių pacientų, su ne mieloidinių piktybinių navikų gauna chemoterapija.