Finlàndia - finès - Fimea (Suomen lääkevirasto)

ratiopharm gmbh - telmisartan - tabletti - 40 mg - telmisartaani

Finlàndia - finès - Fimea (Suomen lääkevirasto)

ratiopharm gmbh - telmisartan - tabletti - 80 mg - telmisartaani

Finlàndia - finès - Fimea (Suomen lääkevirasto)

teva b.v. - lamivudine, abacavir - tabletti, kalvopäällysteinen - 600 mg / 300 mg - lamivudiini ja abakaviiri

Finlàndia - finès - Fimea (Suomen lääkevirasto)

teva b.v. - efavirenzum,tenofoviri disoproxili phosphas,emtricitabinum - tabletti, kalvopäällysteinen - 600 mg / 200 mg / 245 mg - emtrisitabiini, tenofoviiridisoproksiili ja efavirentsi

Unió Europea - finès - EMA (European Medicines Agency)

roche registration gmbh - pertuzumab, trastuzumab - rintojen kasvaimet - antineoplastiset aineet - early breast cancer (ebc)phesgo is indicated for use in combination with chemotherapy in:the neoadjuvant treatment of adult patients with her2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrencethe adjuvant treatment of adult patients with her2-positive early breast cancer at high risk of recurrencemetastatic breast cancer (mbc)phesgo is indicated for use in combination with docetaxel in adult patients with her2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-her2 therapy or chemotherapy for their metastatic disease.

Unió Europea - finès - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - trastuzumab deruxtecan - rintojen kasvaimet - antineoplastiset aineet - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Finlàndia - finès - Fimea (Suomen lääkevirasto)

sanofi pasteur europe - poliovirus type 1, inactivated, poliovirus type 2, inactivated, poliovirus type 3, inactivated, bordetella pertussis toxoid, adsorbed, bordetella pertussis filamentous haemagglutinin, adsorbed, corynebacterium diphtheriae toxoid, adsorbed, clostridium tetani toxoid, adsorbed - injektioneste, suspensio - kurkkumätä-

Finlàndia - finès - Fimea (Suomen lääkevirasto)

sanofi pasteur europe - haemophilus influenzae b polysaccharide,tetanus toxoid conjugate, bordetella pertussis toxoid, adsorbed, bordetella pertussis filamentous haemagglutinin, adsorbed, corynebacterium diphtheriae toxoid, adsorbed, clostridium tetani toxoid, adsorbed, poliovirus type 1 (mahoney), inactivated, poliovirus type 2 (mef-1), inactivated, poliovirus type 3 (saukett), inactivated - injektiokuiva-aine ja suspensio, suspensiota varten - kurkkumätä-

Finlàndia - finès - Fimea (Suomen lääkevirasto)

grÜnenthal gmbh - esomeprazole sodium - injektio/infuusiokuiva-aine, liuosta varten - 40 mg - esomepratsoli

Finlàndia - finès - Fimea (Suomen lääkevirasto)

mylan ireland limited mylan ireland limited - esomeprazolum natricum - injektio/infuusiokuiva-aine, liuosta varten - 40 mg - esomepratsoli