Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

belpharma s.a. - tasonerminas - sarkoma - immunostimulants, - beromun yra nurodyta, suaugusiems, kaip papildoma priemonė siekiant chirurgija vėliau pašalinamas navikas, siekiant išvengti arba atidėti amputacija, arba palaikomoji situacija, irresectable minkštųjų audinių sarkoma galūnių, naudojama kartu su melphalan per lengvas hyperthermic izoliuotos galūnės perfuzijos (ilp).

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

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.

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

corpus medica, uab - ibuprofenas - plėvele dengtos tabletės - 400 mg - ibuprofen

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

alnylam netherlands b.v. - vutrisiran sodium - amyloid neuropathies, familial - kiti nervų sistemos vaistai - treatment of hereditary transthyretin-mediated amyloidosis (hattr amyloidosis) in adult patients with stage 1 or stage 2 polyneuropathy.

Lietuva - lietuvių - Ecolab

ecolab deutschland gmbh -

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

ecolab sp.z o.o., ul. opolska 114, pl-31323 krakow (lenkija). - troklozennatrio dihidratas, natrio dichlorizocianurato dihidratas, dicd - veikliosios medžiagos cas nr.: 51580-86-0, eb nr.: 220-767-7, veikliosios medžiagos pavadinimas: troklozennatrio dihidratas, natrio dichlorizocianurato dihidratas, dicd, koncentracija: 99.61% , veiklioji - maisto ir pašarų sritis

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

ecolab sp.z o.o., ul. opolska 114, pl-31323 krakow (lenkija). - natrio dichlorizocianurato dihidratas - veikliosios medžiagos cas nr.: 51580-86-0, eb nr.: 220-767-7, veikliosios medžiagos pavadinimas: natrio dichlorizocianurato dihidratas, koncentracija: 99.61% , veiklioji - maisto ir pašarų sritis

Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

ecolab sp.z o.o., ul. opolska 114, pl-31323 krakow, lenkija. - troklozennatrio dihidratas, natrio dichlorizocianurato dihidratas, dicd - veikliosios medžiagos cas nr.: 51580-86-0, eb nr.: 220-767-7, veikliosios medžiagos pavadinimas: troklozennatrio dihidratas, natrio dichlorizocianurato dihidratas, dicd, koncentracija: 99.61% , veiklioji - maisto ir pašarų sritis

Europos Sąjunga - lietuvių - 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.

Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

seqirus netherlands b.v. - a/darwin/9/2021 (h3n2) - like strain (a/darwin/6/2021, ivr-227) / a/victoria/4897/2022 (h1n1) pdm09-like strain (a/victoria/4897/2022, ivr-238) / b/phuket/3073/2013-like strain (b/phuket/3073/2013, bvr-1b) / influenza virus b/austria/1359417/2021-like strain (b/austria/1359417/2021, bvr-26) - gripas, žmogus - vakcinos - profilaktikai gripo vyresnio amžiaus (65 metų amžiaus ir vyresni). fluad tetra turėtų būti naudojami laikantis oficialių rekomendacijų.