Caspofungin Mylan 50 mg Norwegia - Norwegia - Statens legemiddelverk

caspofungin mylan 50 mg

mylan ireland limited - kaspofunginacetat - pulver til konsentrat til infusjonsvæske, oppløsning - 50 mg

Caspofungin Mylan 70 mg Norwegia - Norwegia - Statens legemiddelverk

caspofungin mylan 70 mg

mylan ireland limited - kaspofunginacetat - pulver til konsentrat til infusjonsvæske, oppløsning - 70 mg

Dexamethasone Krka 4 mg Norwegia - Norwegia - Statens legemiddelverk

dexamethasone krka 4 mg

krka, d.d. novo mesto - deksametason - tablett - 4 mg

Voltaren 50 mg Norwegia - Norwegia - Statens legemiddelverk

voltaren 50 mg

novartis norge (2) - diklofenaknatrium - enterotablett - 50 mg

Voltaren 25 mg Norwegia - Norwegia - Statens legemiddelverk

voltaren 25 mg

novartis norge (2) - diklofenaknatrium - enterotablett - 25 mg

Voltarol Forte 23.2 mg/ g Norwegia - Norwegia - Statens legemiddelverk

voltarol forte 23.2 mg/ g

haleon denmark aps - diklofenakdietylamin - gel - 23.2 mg/ g

Fluad Tetra Uni Eropa - Norwegia - EMA (European Medicines Agency)

fluad tetra

seqirus netherlands b.v. - a/darwin/9/2021 (h3n2) - like strain (a/darwin/6/2021, ivr-227) / a/victoria/4897/2022 (h1n1) pdm09-like strain (a/victoria/4897/2022, ivr-238) / b/phuket/3073/2013-like strain (b/phuket/3073/2013, bvr-1b) / influenza virus b/austria/1359417/2021-like strain (b/austria/1359417/2021, bvr-26) - influensa, human - vaksiner - forebygging av influensa hos eldre (65 år og eldre). fluad tetra bør brukes i samsvar med offisielle anbefalinger.

Haemate 250 IE / 600 IE Norwegia - Norwegia - Statens legemiddelverk

haemate 250 ie / 600 ie

csl behring gmbh - koagulasjonsfaktor viii, human / von willebrandfaktor, human - pulver og væske til injeksjons-/infusjonsvæske, oppløsning - 250 ie / 600 ie

Breyanzi Uni Eropa - Norwegia - EMA (European Medicines Agency)

breyanzi

bristol-myers squibb pharma eeig - cd19-directed genetically modified autologous cell-based product consisting of purified cd8+ t-cells (cd8+ cells), cd19-directed genetically modified autologous cell-based product consisting of purified cd4+ t cells (cd4+ cells) - lymphoma, large b-cell, diffuse; lymphoma, follicular; mediastinal neoplasms - antineoplastiske midler - breyanzi is indicated for the treatment of adult patients with diffuse large b-cell lymphoma (dlbcl), high grade b-cell lymphoma (hgbcl), primary mediastinal large b-cell lymphoma (pmbcl) and follicular lymphoma grade 3b (fl3b), who relapsed within 12 months from completion of, or are refractory to, first-line chemoimmunotherapy.

Tevimbra Uni Eropa - Norwegia - EMA (European Medicines Agency)

tevimbra

novartis europharm limited - tislelizumab - esophageal squamous cell carcinoma - antineoplastiske midler - oesophageal squamous cell carcinoma (oscc) tevimbra as monotherapy is indicated for the treatment of adult patients with unresectable, locally advanced or metastatic oesophageal squamous cell carcinoma after prior platinum-based chemotherapy.