Imfinzi Európska únia - slovenčina - EMA (European Medicines Agency)

imfinzi

astrazeneca ab - durvalumab - karcinóm, pľúc bez malých buniek - antineoplastické činidlá - non-small cell lung cancer (nsclc)imfinzi as monotherapy is indicated for the treatment of locally advanced, unresectable non small cell lung cancer (nsclc) in adults whose tumours express pd-l1 on ≥ 1% of tumour cells and whose disease has not progressed following platinum based chemoradiation therapy (see section 5. imfinzi in combination with tremelimumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic nsclc with no sensitising egfr mutations or alk positive mutations. small cell lung cancer (sclc)imfinzi in combination with etoposide and either carboplatin or cisplatin is indicated for the first-line treatment of adults with extensive-stage small cell lung cancer (es-sclc). biliary tract cancer (btc)imfinzi in combination with gemcitabine and cisplatin is indicated for the first line treatment of adults with unresectable or metastatic biliary tract cancer (btc). hepatocellular carcinoma (hcc)imfinzi in combination with tremelimumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc).

Enhertu Európska únia - slovenčina - EMA (European Medicines Agency)

enhertu

daiichi sankyo europe gmbh - trastuzumab deruxtecan - neoplazmy prsníkov - antineoplastické činidlá - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Imjudo Európska únia - slovenčina - EMA (European Medicines Agency)

imjudo

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - antineoplastické činidlá - imjudo in combination with durvalumab is indicated for the first line treatment of adults with advanced or unresectable hepatocellular carcinoma (hcc). imjudo in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Tremelimumab AstraZeneca Európska únia - slovenčina - EMA (European Medicines Agency)

tremelimumab astrazeneca

astrazeneca ab - tremelimumab - karcinóm, pľúc bez malých buniek - antineoplastické činidlá - tremelimumab astrazeneca in combination with durvalumab and platinum-based chemotherapy is indicated for the first-line treatment of adults with metastatic non-small cell lung cancer (nsclc) with no sensitising egfr mutations or alk positive mutations.

Giotrif Európska únia - slovenčina - EMA (European Medicines Agency)

giotrif

boehringer ingelheim international gmbh - afatinib - karcinóm, pľúc bez malých buniek - antineoplastické činidlá - giotrif ako monotherapy je indikovaný na liečbu ofepidermal growth factor receptor (egfr) tki-insitného dospelých pacientov s lokálne pokročilým alebo metastatickým non-small cell lung cancer (nsclc) s aktiváciou egfr mutácií(s);lokálne pokročilým alebo metastatickým nsclc z karcinómom histology pokračuje na alebo po platinum-založené chemoterapia.

MOVALIS 15 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

movalis 15 mg

boehringer ingelheim international gmbh, nemecko - meloxikam - 29 - antirheumatica, antiphlogistica, antiuratica

MOVALIS 15 mg/1,5 ml Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

movalis 15 mg/1,5 ml

boehringer ingelheim international gmbh, nemecko - meloxikam - 29 - antirheumatica, antiphlogistica, antiuratica

Recoxa 15 Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

recoxa 15

zentiva a.s., slovensko - meloxikam - 29 - antirheumatica, antiphlogistica, antiuratica

Meloxicam Viatris 15 mg Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

meloxicam viatris 15 mg

viatris limited, Írsko - meloxikam - 29 - antirheumatica, antiphlogistica, antiuratica

Lormed 7,5 Slovensko - slovenčina - ŠÚKL (Štátny ústav pre kontrolu liečiv)

lormed 7,5

pro.med.cs praha a.s., Česká republika - meloxikam - 29 - antirheumatica, antiphlogistica, antiuratica