Holoxan 40 mg/ml Infusionsvätska, lösning Thụy Điển - Tiếng Thụy Điển - 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 Thụy Điển - Tiếng Thụy Điển - 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 Thụy Điển - Tiếng Thụy Điển - 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 Thụy Điển - Tiếng Thụy Điển - 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 Thụy Điển - Tiếng Thụy Điển - 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 Liên Minh Châu Âu - Tiếng Thụy Điển - 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 Liên Minh Châu Âu - Tiếng Thụy Điển - 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 Liên Minh Châu Âu - Tiếng Thụy Điển - 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 Liên Minh Châu Âu - Tiếng Thụy Điển - 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 Liên Minh Châu Âu - Tiếng Thụy Điển - 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.