PERIOCHIP 2.5 mg hammaslamelli Suomi - suomi - Fimea (Suomen lääkevirasto)

periochip 2.5 mg hammaslamelli

dexcel pharma ltd - chlorhexidini digluconas - hammaslamelli - 2.5 mg - klooriheksidiini

ENALAPRIL ASTIMEX 2.5 mg tabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

enalapril astimex 2.5 mg tabletti

dexcel pharma ltd - enalaprili maleas - tabletti - 2.5 mg - enalapriili

ENALAPRIL ASTIMEX 5 mg tabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

enalapril astimex 5 mg tabletti

dexcel pharma ltd - enalaprili maleas - tabletti - 5 mg - enalapriili

ENALAPRIL ASTIMEX 10 mg tabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

enalapril astimex 10 mg tabletti

dexcel pharma ltd - enalaprili maleas - tabletti - 10 mg - enalapriili

ENALAPRIL ASTIMEX 20 mg tabletti Suomi - suomi - Fimea (Suomen lääkevirasto)

enalapril astimex 20 mg tabletti

dexcel pharma ltd - enalaprili maleas - tabletti - 20 mg - enalapriili

Dexmedetomidine Altan Pharma 4 mikrog/ml infuusioneste, liuos Suomi - suomi - Fimea (Suomen lääkevirasto)

dexmedetomidine altan pharma 4 mikrog/ml infuusioneste, liuos

altan pharma ltd - dexmedetomidine hydrochloride - infuusioneste, liuos - 4 mikrog/ml - deksmedetomidiini

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

imprida

novartis europharm ltd - valsartan, amlodipine (as amlodipine besilate) - verenpainetauti - reniini-angiotensiinijärjestelmään vaikuttavat aineet - essentiaalisen hypertension hoito. imprida on tarkoitettu potilaille, joiden verenpaine ei laske riittävästi yksinomaan amlodipiinilla tai valsartaanilla.

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

oyavas

stada arzneimittel ag - bevasitsumabi - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiset aineet - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. lisätietoja ihmisen epidermaalisen kasvutekijäreseptorin 2 (her2) tilasta on kohdassa 5. oyavas in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with oyavas in combination with capecitabine. lisätietoja her2-tilasta on kohdassa 5. oyavas, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer other than predominantly squamous cell histology. oyavas, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. oyavas, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents. oyavas, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. oyavas, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.

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

dacogen

janssen-cilag international n.v.   - decitabine - leukemia, myeloidi - antineoplastiset aineet - uusien diagnosoitujen de novo tai toissijainen akuutti myelooinen leukemia (aml) maailman terveysjärjestön (who)-luokituksen mukaisesti aikuisten potilaille, jotka eivät ole ehdolla standardin induktio solunsalpaajahoitoa.