Bupivacaine Baxter Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

bupivacaine baxter

baxter holding b.v. - bupivakaino hidrochloridas - injekcinis tirpalas - 2,5 mg/ml - bupivacaine

Bupivacaine Accord Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

bupivacaine accord

accord healthcare b.v. - bupivakainas - injekcinis tirpalas - 2,5 mg/ml; 5 mg/ml - bupivacaine

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

elocon

n.v. organon - mometazono furoatas - tepalas - 1 mg/g - mometasone

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

cuprymina

a.c.o.m. - advanced center oncology - varis (64cu) chloridas - radionuklidų vaizdavimas - various diagnostic radiopharmaceuticals - cuprymina yra radioaktyviųjų preparatų pirmtakas. jis nėra skirtas pacientams tiesiogiai vartoti. Šis vaistinis preparatas turi būti naudojamas tik radioaktyviai žymimoms nešiklio molekulėms, kurios buvo specialiai sukurtos ir patvirtintos radionuklidui žymėti.

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

kyleena

bayer ag - levonorgestrelis - vartojimo į gimdos ertmę sistema - 19,5 mg - plastic iud with progestogen

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

oxycort

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

BUPIVACAINUM WZF Polfa Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

bupivacainum wzf polfa

warszawskie zakłady farmaceutyczne polfa s.a. - bupivakainas - injekcinis tirpalas - 5 mg/ml - bupivacaine

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

fleree

bayer ag - levonorgestrelis - vartojimo į gimdos ertmę sistema - 13,5 mg - plastic iud with progestogen

Exparel liposomal Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

exparel liposomal

pacira ireland limited - bupivacaine - acute pain - amides, anesthetics, local - exparel liposomal is indicated:in adults as a brachial plexus block or femoral nerve block for treatment of post-operative pain. in adults and children aged 6 years or older as a field block for treatment of somatic post-operative pain from small- to medium-sized surgical wounds.

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.