Sendolor 10 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sendolor 10 mg/ml injektionsvæske, opløsning

eurocept international b.v. - morphinhydrochloridtrihydrat - injektionsvæske, opløsning - 10 mg/ml

Amsalyo 75 mg pulver til koncentrat til infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

amsalyo 75 mg pulver til koncentrat til infusionsvæske, opløsning

eurocept international b.v. - amsacrin - pulver til koncentrat til infusionsvæske, opløsning - 75 mg

Sendolor 1 mg/ml infusionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sendolor 1 mg/ml infusionsvæske, opløsning

eurocept international b.v. - morphinhydrochloridtrihydrat - infusionsvæske, opløsning - 1 mg/ml

Ketamal 10 mg/ml injektionsv?ske, opl?sning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

ketamal 10 mg/ml injektionsv?ske, opl?sning

eurocept international b.v. - ketaminhydrochlorid - injektionsvæske, opløsning - 10 mg/ml

Sendolor 1 mg/ml injektionsvæske, opløsning Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sendolor 1 mg/ml injektionsvæske, opløsning

eurocept international b.v. - morphinhydrochloridtrihydrat - injektionsvæske, opløsning - 1 mg/ml

Thiotepa Riemser Den Europæiske Union - dansk - EMA (European Medicines Agency)

thiotepa riemser

esteve pharmaceuticals gmbh - thiotepa - hematopoietic stem cell transplantation; neoplasms - antineoplastiske midler - thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients. thiotepa riemser is indicated, in combination with other chemotherapy medicinal products:with or without total body irradiation (tbi), as conditioning treatment prior to allogeneic or autologous haematopoietic progenitor cell transplantation (hpct) in haematological diseases in adult and paediatric patients;when high dose chemotherapy with hpct support is appropriate for the treatment of solid tumours in adult and paediatric patients.

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

rybrevant

janssen-cilag international n.v.    - amivantamab - carcinom, ikke-småcellet lunge - antineoplastiske midler - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.