Suomi - suomi - Fimea (Suomen lääkevirasto)

therabel s.a. - tramadoli hydrochloridum - injektioneste, liuos - 50 mg/ml - tramadoli

Suomi - suomi - Fimea (Suomen lääkevirasto)

therabel s.a. - tramadoli hydrochloridum - kapseli, kova - 50 mg - tramadoli

Suomi - suomi - Fimea (Suomen lääkevirasto)

therabel s.a. - tramadoli hydrochloridum - peräpuikko - 100 mg - tramadoli

Euroopan unioni - suomi - EMA (European Medicines Agency)

taw pharma (ireland) limited - klopidogreelin hydrokloridi - peripheral vascular diseases; stroke; myocardial infarction; acute coronary syndrome - antitromboottiset aineet - , , , , secondary prevention of atherothrombotic events, , clopidogrel is indicated in: , - adult patients suffering from myocardial infarction (from a few days until less than 35 days), ischaemic stroke (from 7 days until less than 6 months) or established peripheral arterial disease. , - adult patients suffering from acute coronary syndrome:,    - non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). ,     - st segment elevation acute myocardial infarction, in combination with asa in medically treated patients eligible for thrombolytic therapy. , , in patients with moderate to high-risk transient ischaemic attack (tia) or minor ischaemic stroke (is), clopidogrel in combination with asa is indicated in:, - adult patients with moderate to high-risk tia (abcd2  score ≥4) or minor is (nihss  ≤3) within 24 hours of either the tia or is event.  , , prevention of atherothrombotic and thromboembolic events in atrial fibrillation, in adult patients with atrial fibrillation who have at least one risk factor for vascular events, are not suitable for treatment with vitamin k antagonists (vka) and who have a low bleeding risk, clopidogrel is indicated in combination with asa for the prevention of atherothrombotic and thromboembolic events, including stroke. , , for further information please refer to section 5. , , ,.

Euroopan unioni - suomi - EMA (European Medicines Agency)

accord healthcare s.l.u. - dasatinibin - precursor cell lymphoblastic leukemia-lymphoma; leukemia, myelogenous, chronic, bcr-abl positive - antineoplastiset aineet - dasatinib accordpharma is indicated for the treatment of adult patients with: newly diagnosed philadelphia chromosome positive (ph+) chronic myelogenous leukaemia (cml) in the chronic phase.  chronic, accelerated or blast phase cml with resistance or intolerance to prior therapy including imatinib.  ph+ acute lymphoblastic leukaemia (all) and lymphoid blast cml with resistance or intolerance to prior therapy. dasatinib accordpharma is indicated for the treatment of paediatric patients with: newly diagnosed ph+ cml in chronic phase (ph+ cml-cp) or ph+ cml-cp resistant or intolerant to prior therapy including imatinib.  newly diagnosed ph+ all in combination with chemotherapy.

Euroopan unioni - suomi - EMA (European Medicines Agency)

teva b.v. - zoledronihappoa - osteoporosis; osteitis deformans; osteoporosis, postmenopausal - lääkkeet luusairauksien hoitoon - treatment of osteoporosis: , in post-menopausal women;, in men; , at increased risk of fracture including those with a recent low-trauma hip fracture. treatment of osteoporosis associated with long-term systemic glucocorticoid therapy: , in post-menopausal women;, in men; , at increased risk of fracture. hoitoon pagetin tauti luu aikuisilla.

Euroopan unioni - suomi - EMA (European Medicines Agency)

teva b.v.  - lamivudiini - hiv-infektiot - antiviraalit systeemiseen käyttöön - lamivudine teva pharma b. on merkitty osana antiretroviraalista yhdistelmähoitoa ihmisen immuunikatoviruksen (hiv) infektoituneiden aikuisten ja lasten hoitoon.

Euroopan unioni - suomi - EMA (European Medicines Agency)

teva b.v. - ribaviriini - hepatiitti c, krooninen - antiviraalit systeemiseen käyttöön - ribavirin teva pharma b. is indicated in combination with other medicinal products for the treatment ofchronic hepatitis c (chc) in adults (see sections 4. 2, 4. 4, ja 5. ribavirin teva pharma b. is indicated in combination with other medicinal products for the treatment ofchronic hepatitis c (chc) for paediatric patients (children 3 years of age and older and adolescents) notpreviously treated and without liver decompensation (see sections 4. 2, 4. 4 ja 5.

Euroopan unioni - suomi - EMA (European Medicines Agency)

pharmathen s.a. - ibandronihappo - hypercalcemia; fractures, bone; neoplasm metastasis; breast neoplasms - lääkkeet luusairauksien hoitoon - concentrate for solution for infusion prevention of skeletal events (pathological fractures, bone complications requiring radiotherapy or surgery) in patients with breast cancer and bone metastases. kasvainten aiheuttaman hyperkalsemian hoitoon tai ilman etäpesäkkeitä. film-coated tablets prevention of skeletal events (pathological fractures, bone complications requiring radiotherapy or surgery) in patients with breast cancer and bone metastases.

Euroopan unioni - suomi - EMA (European Medicines Agency)

ferring pharmaceuticals a/s - degareliksia - prostatiset kasvaimet - endokriinihoito - firmagon is a gonadotrophin releasing hormone (gnrh) antagonist indicated:- for treatment of adult male patients with advanced hormone-dependent prostate cancer. - for treatment of high-risk localised and locally advanced hormone dependent prostate cancer in combination with radiotherapy. - as neo-adjuvant treatment prior to radiotherapy in patients with high-risk localised or locally advanced hormone dependent prostate cancer.