Holoxan 40 mg/ml Infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

holoxan 40 mg/ml infusionsvätska, lösning

baxter medical ab - ifosfamid - infusionsvätska, lösning - 40 mg/ml - ifosfamid 40 mg aktiv substans - ifosfamid

Holoxan Pulver till injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

holoxan pulver till injektions-/infusionsvätska, lösning

paranova läkemedel ab - ifosfamid - pulver till injektions-/infusionsvätska, lösning - ifosfamid 1 mg aktiv substans

Holoxan Pulver till injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

holoxan pulver till injektions-/infusionsvätska, lösning

paranova läkemedel ab - ifosfamid - pulver till injektions-/infusionsvätska, lösning - ifosfamid 1 mg aktiv substans

Cyclophosphamide Accord 500 mg Pulver till injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

cyclophosphamide accord 500 mg pulver till injektions-/infusionsvätska, lösning

accord healthcare b.v. - cyklofosfamidmonohydrat - pulver till injektions-/infusionsvätska, lösning - 500 mg - cyklofosfamidmonohydrat 534 mg aktiv substans; mannitol hjälpämne

Cyclophosphamide Accord 1000 mg Pulver till injektions-/infusionsvätska, lösning Sverige - svenska - Läkemedelsverket (Medical Products Agency)

cyclophosphamide accord 1000 mg pulver till injektions-/infusionsvätska, lösning

accord healthcare b.v. - cyklofosfamidmonohydrat - pulver till injektions-/infusionsvätska, lösning - 1000 mg - mannitol hjälpämne; cyklofosfamidmonohydrat 1069 mg aktiv substans

Columvi Europeiska unionen - svenska - EMA (European Medicines Agency)

columvi

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - antineoplastiska medel - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.

Lunsumio Europeiska unionen - svenska - EMA (European Medicines Agency)

lunsumio

roche registration gmbh - mosunetuzumab - lymfom, follikel - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

Tecvayli Europeiska unionen - svenska - EMA (European Medicines Agency)

tecvayli

janssen-cilag international n.v. - teclistamab - multipelt myelom - antineoplastiska medel - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Talvey Europeiska unionen - svenska - EMA (European Medicines Agency)

talvey

janssen-cilag international n.v. - talquetamab - multipelt myelom - antineoplastiska medel - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Tepkinly Europeiska unionen - svenska - EMA (European Medicines Agency)

tepkinly

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antineoplastiska medel - tepkinly as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b-cell lymphoma (dlbcl) after two or more lines of systemic therapy.