Tagrisso Den Europæiske Union - dansk - EMA (European Medicines Agency)

tagrisso

astrazeneca ab - osimertinib mesilate - carcinom, ikke-småcellet lunge - andre antineoplastiske midler, protein kinase hæmmere - tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations- the first-line treatment of adult patients nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc. tagrisso as monotherapy is indicated for:- the adjuvant treatment after complete tumour resection in adult patients with stage ib-iiia non-small cell lung cancer (nsclc) whose tumours have epidermal growth factor receptor (egfr) exon 19 deletions or exon 21 (l858r) substitution mutations. - the first-line treatment of adult patients with locally advanced or metastatic nsclc with activating egfr mutations. - the treatment of adult patients with locally advanced or metastatic egfr t790m mutation-positive nsclc.

Ondexxya Den Europæiske Union - dansk - EMA (European Medicines Agency)

ondexxya

astrazeneca ab - andexanet alfa - stof-relaterede bivirkninger og bivirkninger - alle andre terapeutiske produkter - til voksne patienter, der er behandlet med en direkte faktor xa (fxa) - hæmmer (apixaban eller rivaroxaban), når tilbageførsel af antikoagulation er nødvendig på grund af livstruende eller ukontrolleret blødning.

Lumoxiti Den Europæiske Union - dansk - EMA (European Medicines Agency)

lumoxiti

astrazeneca ab - moxetumomab pasudotox - leukæmi, hårete celler - antineoplastiske midler - lumoxiti as monotherapy is indicated for the treatment of adult patients with relapsed or refractory hairy cell leukaemia (hcl) after receiving at least two prior systemic therapies, including treatment with a purine nucleoside analogue (pna).

Evusheld Den Europæiske Union - dansk - EMA (European Medicines Agency)

evusheld

astrazeneca ab - tixagevimab, cilgavimab - covid-19 virus infection - prevention of covid-19.

Imjudo Den Europæiske Union - dansk - EMA (European Medicines Agency)

imjudo

astrazeneca ab - tremelimumab - carcinoma, hepatocellular - antineoplastiske midler - 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.

Bambec 10 mg tabletter Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

bambec 10 mg tabletter

astrazeneca a/s - bambuterolhydrochlorid - tabletter - 10 mg

Bricanyl 2,5 mg/ml inhalationsvæske til nebulisator, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

bricanyl 2,5 mg/ml inhalationsvæske til nebulisator, opløsning

astrazeneca a/s - terbutalinsulfat - inhalationsvæske til nebulisator, opløsning - 2,5 mg/ml

Bricanyl 0,5 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

bricanyl 0,5 mg/ml injektionsvæske, opløsning

astrazeneca a/s - terbutalinsulfat - injektionsvæske, opløsning - 0,5 mg/ml