Avrupa Birliği - Fince - EMA (European Medicines Agency)

astrazeneca ab - metformiinihydrokloridi, saxagliptin dapagliflotsiini - diabetes mellitus, tyyppi 2 - diabeetilla käytettävät lääkkeet - qtrilmet on tarkoitettu aikuisille 18-vuotiaat ja vanhemmat, joilla on tyypin 2 diabetes:parantaa sokeritasapainoa, kun metformiinin kanssa tai ilman sulfonyyliureoiden (su) ja joko saxagliptin tai dapagliflotsiini ei anna riittävää glukoositasapainoa. kun jo hoidettiin metformiinilla ja saxagliptin ja dapagliflotsiini.

Avrupa Birliği - Fince - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - multiple myeloma - antineoplastiset aineet - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Finlandiya - Fince - Fimea (Suomen lääkevirasto)

bayer ag -

Avrupa Birliği - Fince - EMA (European Medicines Agency)

bayer ag - finerenone - renal insufficiency, chronic; diabetes mellitus, type 2 - reniini-angiotensiinijärjestelmään vaikuttavat aineet - kerendia is indicated for the treatment of chronic kidney disease (stage 3 and 4 with albuminuria) associated with type 2 diabetes in adults.

Avrupa Birliği - Fince - EMA (European Medicines Agency)

laboratorios lesvi s.l. - dimetyylifumaraatti - multippeliskleroosi, relapsoiva-remittoiva - immunosuppressantit - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Avrupa Birliği - Fince - EMA (European Medicines Agency)

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

Avrupa Birliği - Fince - EMA (European Medicines Agency)

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - diabeetilla käytettävät lääkkeet - type 2 diabetes mellitusdapagliflozin viatris is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 diabetes. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 ja 5. heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Avrupa Birliği - Fince - EMA (European Medicines Agency)

fennec pharmaceuticals (eu) limited - sodium thiosulfate - ear diseases; ototoxicity - kaikki muut terapeuttiset tuotteet - pedmarqsi is indicated for the prevention of ototoxicity induced by cisplatin chemotherapy in patients 1 month to < 18 years of age with localised, non-metastatic, solid tumours.

Avrupa Birliği - Fince - EMA (European Medicines Agency)

accord healthcare s.l.u. - tolvaptaanille - epäkelpo adh-oireyhtymä - diureetit, - tolvaptan is indicated in adults for the treatment of hyponatremia secondary to the syndrome of inappropriate antidiuretic hormone secretion (siadh).

Finlandiya - Fince - Fimea (Suomen lääkevirasto)

le vet. beheer b.v. - clenbuterol hydrochloride - siirappi - 25 mikrog/ml - klenbuteroli