Symbicort 160 mikrog/ dose / 4.5 mikrog/ dose Noregur - norska - Statens legemiddelverk

symbicort 160 mikrog/ dose / 4.5 mikrog/ dose

astrazeneca - budesonid / formoterolfumaratdihydrat - inhalasjonsaerosol, suspensjon - 160 mikrog/ dose / 4.5 mikrog/ dose

Symbicort Mite Turbuhaler 80 mikrog/ dose / 4.5 mikrog/ dose Noregur - norska - Statens legemiddelverk

symbicort mite turbuhaler 80 mikrog/ dose / 4.5 mikrog/ dose

astrazeneca - budesonid / formoterolfumaratdihydrat - inhalasjonspulver - 80 mikrog/ dose / 4.5 mikrog/ dose

Symbicort Turbuhaler 160 mikrog/ dose / 4.5 mikrog/ dose Noregur - norska - Statens legemiddelverk

symbicort turbuhaler 160 mikrog/ dose / 4.5 mikrog/ dose

astrazeneca - budesonid / formoterolfumaratdihydrat - inhalasjonspulver - 160 mikrog/ dose / 4.5 mikrog/ dose

Symbicort Forte Turbuhaler 320 mikrog/ dose / 9 mikrog/ dose Noregur - norska - Statens legemiddelverk

symbicort forte turbuhaler 320 mikrog/ dose / 9 mikrog/ dose

astrazeneca - budesonid / formoterolfumaratdihydrat - inhalasjonspulver - 320 mikrog/ dose / 9 mikrog/ dose

Xylocain 2 % Noregur - norska - Statens legemiddelverk

xylocain 2 %

aspen pharma trading limited - lidokainhydrokloridmonohydrat - gel - 2 %

Xylocain 5 % Noregur - norska - Statens legemiddelverk

xylocain 5 %

aspen pharma trading limited - lidokain - salve - 5 %

Xylocain 100 mg/ ml Noregur - norska - Statens legemiddelverk

xylocain 100 mg/ ml

aspen pharma trading limited - lidokain - spray - 100 mg/ ml

Imfinzi Evrópusambandið - norska - EMA (European Medicines Agency)

imfinzi

astrazeneca ab - durvalumab - karsinom, ikke-småcellet lunge - antineoplastiske midler - 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).

Bevespi Aerosphere Evrópusambandið - norska - EMA (European Medicines Agency)

bevespi aerosphere

astrazeneca ab - glycopyrronium, formoterol fumarate dihydrate - lungesykdom, kronisk obstruktiv - formoterol og glycopyrronium bromide - bevespi aerosphere er angitt som en vedlikehold bronkodilaterende behandling for å lindre symptomer hos voksne pasienter med kronisk obstruktiv lungesykdom (kols).

Ondexxya Evrópusambandið - norska - EMA (European Medicines Agency)

ondexxya

astrazeneca ab - andexanet alfa - narkotika-relaterte bivirkninger og uønskede reaksjoner - alle andre terapeutiske produkter - for voksne pasienter behandlet med en direkte faktor xa (anl) inhibitor (apixaban eller rivaroxaban) når reversering av antikoagulasjonsbehandling er nødvendig på grunn av livstruende eller ukontrollert blødning.