Convulex Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

convulex

g.l. pharma gmbh - natrio valproatas - injekcinis ar infuzinis tirpalas - 100 mg/ml; 50 mg/ml; 500 mg; 150 mg; 300 mg/ml - valproic acid

Ubistesin Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

ubistesin

pierrel s.p.a. - artikainas/epinefrinas - injekcinis tirpalas - 40 mg/5 µg/ml; 40 mg/10 µg/ml - articaine, combinations

Valproate sodium Sandoz Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

valproate sodium sandoz

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

METHYLPREDNISOLONE SOPHARMA Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

methylprednisolone sopharma

sopharma ad - metilprednizolonas - milteliai ir tirpiklis injekciniam ar infuziniam tirpalui - 250 mg - methylprednisolone

Depakine Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

depakine

sanofi winthrop industrie - natrio valproatas - sirupas - 57,64 mg/ml - valproic acid

DEPAKINE CHRONO Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

depakine chrono

sanofi-aventis lietuva, uab - natrio valproatas - modifikuoto atpalaidavimo tabletės - 500 mg; 300 mg - valproic acid

DESIRETT Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

desirett

exeltis baltics, uab - dezogestrelis - plėvele dengtos tabletės - 75 µg - desogestrel

Cerazette Литва - литовский - SMCA (Valstybinė vaistų kontrolės tarnyba)

cerazette

merck sharp & dohme b.v. - dezogestrelis - plėvele dengtos tabletės - 75 µg - desogestrel

Abevmy Европейский союз - литовский - EMA (European Medicines Agency)

abevmy

biosimilar collaborations ireland limited - 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 - abevmy in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. abevmy 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. abevmy 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 abevmy in combination with capecitabine. daugiau informacijos apie her2 statusą rasite 5 skyriuje. abevmy, 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 other than predominantly squamous cell histology. abevmy, in combination with erlotinib, is indicated for first-line treatment of adult patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. abevmy in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. abevmy, 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. abevmy, 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 vegf inhibitors or vegf receptor–targeted agents. abevmy 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. abevmy, 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.

Lextemy Европейский союз - литовский - EMA (European Medicines Agency)

lextemy

mylan ire healthcare limited - 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 - treatment of carcinoma of the colon or rectum, breast cancer, non-small cell lung cancer, renal cell cancer, epithelial ovarian, fallopian tube or primary peritoneal cancer, and carcinoma of the cervix.