Valaciclovir Sandoz 500 mg Norge - norsk - Statens legemiddelverk

valaciclovir sandoz 500 mg

sandoz a/s - valaciklovirhydroklorid - tablett, filmdrasjert - 500 mg

Valaciclovir Sandoz 250 mg Norge - norsk - Statens legemiddelverk

valaciclovir sandoz 250 mg

sandoz a/s - valaciklovirhydroklorid - tablett, filmdrasjert - 250 mg

Viramune 400 mg Norge - norsk - Statens legemiddelverk

viramune 400 mg

abacus medicine a/s - nevirapin - depottablett - 400 mg

Zovirax 800 mg Norge - norsk - Statens legemiddelverk

zovirax 800 mg

glaxosmithkline as - aciklovir - tablett - 800 mg

Zovirax 80 mg/ ml Norge - norsk - Statens legemiddelverk

zovirax 80 mg/ ml

glaxosmithkline as - aciklovir - mikstur, suspensjon - 80 mg/ ml

Zovirax 200 mg Norge - norsk - Statens legemiddelverk

zovirax 200 mg

glaxosmithkline as - aciklovir - tablett - 200 mg

Darunavir Accord 600 mg Norge - norsk - Statens legemiddelverk

darunavir accord 600 mg

accord healthcare b.v. - darunavirpropylenglykolat - tablett, filmdrasjert - 600 mg

Zovirax 800 mg Norge - norsk - Statens legemiddelverk

zovirax 800 mg

2care4 aps - aciklovir - tablett - 800 mg

Zercepac Den europeiske union - norsk - EMA (European Medicines Agency)

zercepac

accord healthcare s.l.u. - trastuzumab - breast neoplasms; stomach neoplasms - antineoplastiske midler - breast cancermetastatic breast cancer zercepac is indicated for the treatment of adult patients with her2 positive metastatic breast cancer (mbc):as monotherapy for the treatment of those patients who have received at least two chemotherapy regimens for their metastatic disease. før kjemoterapi må ha tatt minst en anthracycline og en taxane med mindre pasienter er uegnet for disse behandlingene. hormon reseptor positive pasienter må også ha mislyktes hormonell behandling, med mindre pasienter er uegnet for disse behandlingene.                      in combination with paclitaxel for the treatment of those patients who have not received chemotherapy for their metastatic disease and for whom an anthracycline is not suitable. i kombinasjon med docetaxel for behandling av pasienter som ikke har fått kjemoterapi for sine metastatisk sykdom. i kombinasjon med en aromatase inhibitor for behandling av postmenopausale pasienter med hormon-reseptor positiv mbc, som ikke tidligere er behandlet med trastuzumab. early breast cancer zercepac is indicated for the treatment of adult patients with her2 positive early breast cancer (ebc). følgende kirurgi, kjemoterapi (neoadjuvant eller adjuvant) og strålebehandling (hvis relevant). følgende adjuvant kjemoterapi med doxorubicin og cyklofosfamid, i kombinasjon med paclitaxel eller docetaxel. i kombinasjon med adjuvant kjemoterapi som består av docetaxel og carboplatin. in combination with neoadjuvant chemotherapy followed by adjuvant zercepac therapy, for locally advanced (including inflammatory) disease or tumours > 2 cm in diameter. zercepac should only be used in patients with metastatic or early breast cancer whose tumours have either her2 overexpression or her2 gene amplification as determined by an accurate and validated assay. metastatic gastric cancer zercepac in combination with capecitabine or 5-fluorouracil and cisplatin is indicated for the treatment of adult patients with her2 positive metastatic adenocarcinoma of the stomach or gastro-oesophageal junction who have not received prior anti-cancer treatment for their metastatic disease. zercepac should only be used in patients with metastatic gastric cancer (mgc) whose tumours have her2 overexpression as defined by ihc2+ and a confirmatory sish or fish result, or by an ihc 3+ result. nøyaktig og validert analysen metoder bør brukes.

Veklury Den europeiske union - norsk - EMA (European Medicines Agency)

veklury

gilead sciences ireland uc - remdesivir - covid-19 virus infection - veklury is indicated for the treatment of coronavirus disease 2019 (covid 19) in:adults and paediatric patients (at least 4 weeks of age and weighing at least 3 kg) with pneumonia requiring supplemental oxygen (low- or high-flow oxygen or other non-invasive ventilation at start of treatment)adults and paediatric patients (weighing at least 40 kg) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.