Buprefarm 5 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 5 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 5 mikrog/tunti - buprenorfiini

Buprefarm 10 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 10 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 10 mikrog/tunti - buprenorfiini

Buprefarm 20 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 20 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 20 mikrog/tunti - buprenorfiini

Buprefarm 15 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 15 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 15 mikrog/tunti - buprenorfiini

Buprefarm 25 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 25 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 25 mikrog/tunti - buprenorfiini

Buprefarm 30 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 30 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 30 mikrog/tunti - buprenorfiini

Buprefarm 40 mikrog/tunti depotlaastari Suomi - suomi - Fimea (Suomen lääkevirasto)

buprefarm 40 mikrog/tunti depotlaastari

orifarm generics a/s - buprenorphine - depotlaastari - 40 mikrog/tunti - buprenorfiini

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.

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

ciambra

menarini international operations luxembourg s.a. - pemetreksedi dinatrium hemipentahydraatti - carcinoma, non-small-cell lung; mesothelioma - antineoplastiset aineet - malignant pleural mesothelioma ciambra in combination with cisplatin is indicated for the treatment of chemotherapy naïve patients with unresectable malignant pleural mesothelioma. non-small cell lung cancer ciambra in combination with cisplatin is indicated for the first line treatment of patients with locally advanced or metastatic non-small cell lung cancer other than predominantly squamous cell histology. ciambra on tarkoitettu monoterapiana huolto hoito on paikallisesti edennyt tai metastasoitunut ei-pienisoluinen keuhkosyöpä muu kuin levyepiteelikarsinooma hallitsevana tyyppinä potilailla, joiden sairaus ei ole edennyt välittömästi platinapohjaisen kemoterapian. ciambra on tarkoitettu monoterapiana toisen linjan hoidoksi potilaille, joilla on paikallisesti pitkälle edennyt tai metastaattinen ei-pienisoluinen keuhkosyöpä muu kuin levyepiteelikarsinooma hallitsevana tyyppinä.

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

yervoy

bristol-myers squibb pharma eeig - ipilimumabi - melanoma; carcinoma, renal cell; carcinoma, non-small-cell lung; mesothelioma, malignant; colorectal neoplasms - antineoplastiset aineet - melanomayervoy as monotherapy or combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults and adolescents 12 years of age and older (see section 4.  yervoy in combination with nivolumab is indicated for the treatment of advanced (unresectable or metastatic) melanoma in adults. relative to nivolumab monotherapy, an increase in progression-free survival (pfs) and overall survival (os) for the combination of nivolumab with ipilimumab is established only in patients with low tumour pd-l1 expression (see sections 4. 4 ja 5. renal cell carcinoma (rcc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with intermediate/poor-risk advanced renal cell carcinoma (see section 5. non-small cell lung cancer (nsclc)yervoy in combination with nivolumab and 2 cycles of platinum-based chemotherapy is indicated for the first-line treatment of metastatic non-small cell lung cancer in adults whose tumours have no sensitising egfr mutation or alk translocation. malignant pleural mesothelioma (mpm)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable malignant pleural mesothelioma. mismatch repair deficient (dmmr) or microsatellite instability-high (msi-h) colorectal cancer (crc)yervoy in combination with nivolumab is indicated for the treatment of adult patients with mismatch repair deficient or microsatellite instability-high metastatic colorectal cancer after prior fluoropyrimidine based combination chemotherapy (see section 5. oesophageal squamous cell carcinoma (oscc)yervoy in combination with nivolumab is indicated for the first-line treatment of adult patients with unresectable advanced, recurrent or metastatic oesophageal squamous cell carcinoma with tumour cell pd-l1 expression ≥ 1%.