Vegzelma Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

vegzelma

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.

octagam Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

octagam

octapharma (ip) sprl - Žmogaus normalusis imunoglobulinas - infuzinis tirpalas - 100 mg/ml - immunoglobulins, normal human, for intravascular adm.

Valproate sodium Sandoz Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

valproate sodium sandoz

sandoz d.d. - natrio valproatas - pailginto atpalaidavimo tabletės - 500 mg - valproic acid

AMITRIPTYLINE-GRINDEKS Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

amitriptyline-grindeks

as grindeks - amitriptilinas - plėvele dengtos tabletės - 25 mg; 10 mg - amitriptyline

octagam Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

octagam

octapharma (ip) sprl - Žmogaus normalusis imunoglobulinas, intraveninis - infuzinis tirpalas - 50 mg/ml - immunoglobulins, normal human, for intravascular adm.

Agenerase Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

agenerase

glaxo group ltd. - amprenaviras - Živ infekcijos - antivirusiniai vaistai sisteminiam naudojimui - agenerase, kartu su kitais antiretrovirusinis agentai, nurodomas gydymo proteazė inhibitorius (pi) patyrė Živ-1 infekuotiems suaugusiems ir vaikams virš 4 metų metus. agenerase kapsules paprastai reikia vartoti kartu su maža ritonaviro doze, kaip amprenaviro farmakokinetikos stiprintoju (žr. 4 skyrių. 2 ir 4. amprenaviro pasirinkimas turėtų būti pagrįstas atskirais viruso atsparumo tyrimais ir pacientų gydymo istorija (žr. 5 skyrių). naudinga agenerase padidino su ritonaviru nebuvo įrodyta, pi nava pacientams (žr. skyrių 5.

Fraxiparine Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

fraxiparine

lex ano, uab - nadroparino kalcio druska - injekcinis tirpalas - 2850 anti-xa tv/0,3 ml - nadroparin

Fraxiparine Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

fraxiparine

lex ano, uab - nadroparino kalcio druska - injekcinis tirpalas - 5700 anti-xa tv/0,6 ml - nadroparin

EFFIPRO, 2,5 mg/ml, odos purškalas, tirpalas katėms ir šunims Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

effipro, 2,5 mg/ml, odos purškalas, tirpalas katėms ir šunims

virbac s.a. (prancūzija) - purškiamasis odos tirpalas - 1 ml tirpalo yra: fipronilo 2,5 mg. - blusomis, erkėmis ir plaukagraužiais užsikrėtusiems šunims ir katėms gydyti.