Bocouture 50 yksikköä injektiokuiva-aine, liuosta varten Suomi - suomi - Fimea (Suomen lääkevirasto)

bocouture 50 yksikköä injektiokuiva-aine, liuosta varten

merz pharmaceuticals gmbh - clostridium botulinum type a neurotoxin (150kd) - injektiokuiva-aine, liuosta varten - 50 yksikköä - botuliinitoksiini

Bocouture 100 yksikköä injektiokuiva-aine, liuosta varten Suomi - suomi - Fimea (Suomen lääkevirasto)

bocouture 100 yksikköä injektiokuiva-aine, liuosta varten

merz pharmaceuticals gmbh - clostridium botulinum type a neurotoxin (150kd) - injektiokuiva-aine, liuosta varten - 100 yksikköä - botuliinitoksiini

Partoxin vet. 17 mikrog/ml (10 IU/ml) injektioneste, liuos Suomi - suomi - Fimea (Suomen lääkevirasto)

partoxin vet. 17 mikrog/ml (10 iu/ml) injektioneste, liuos

pharmaxim ab - oxytocin - injektioneste, liuos - 17 mikrog/ml (10 iu/ml) - oksitosiini

Pentoxin 400 mg depottabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

pentoxin 400 mg depottabletti

ratiopharm gmbh - pentoxifylline - depottabletti - 400 mg - pentoksifylliini

Eucreas Euroopan unioni - suomi - EMA (European Medicines Agency)

eucreas

novartis europharm limited - vildagliptiini, metformiinihydrokloridia - diabetes mellitus, tyyppi 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) Euroopan unioni - suomi - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - vildagliptiini, metformiinihydrokloridia - diabetes mellitus, tyyppi 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 ja 5. 1 käytettävissä olevista tiedoista eri yhdistelmistä).

Breyanzi Euroopan unioni - suomi - 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 - antineoplastiset aineet - 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.

Lupkynis Euroopan unioni - suomi - EMA (European Medicines Agency)

lupkynis

otsuka pharmaceutical netherlands b.v. - voclosporin - lupus nephritis - immunosuppressantit - lupkynis is indicated in combination with mycophenolate mofetil for the treatment of adult patients with active class iii, iv or v (including mixed class iii/v and iv/v) lupus nephritis (ln).

Abilify Maintena Euroopan unioni - suomi - EMA (European Medicines Agency)

abilify maintena

otsuka pharmaceutical netherlands b.v. - aripipratsolia - skitsofrenia - psyykenlääkkeiden - skitsofrenian ylläpitohoito aikuisilla potilailla stabiloitui oraalisella aripipratsolilla.

Fluad Tetra Euroopan unioni - suomi - 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) - influenssa, ihminen - rokotteet - influenssan ennaltaehkäisyssä iäkkäillä (65-vuotiaat ja sitä vanhemmat). fluad tetra tulee käyttää virallisten suositusten mukaisesti.