Euroopan unioni - suomi - EMA (European Medicines Agency)

bavarian nordic a/s - muunnettu vaccinia ankara - baijerin pohjoismainen (mva-bn) -virus - smallpox vaccine; monkeypox virus - muut virusrokotteet, - active immunisation against smallpox, monkeypox and disease caused by vaccinia virus in adults (see sections 4. 4 ja 5. käyttö tämä rokote tulee virallisten suositusten mukaisesti.

Euroopan unioni - suomi - EMA (European Medicines Agency)

janssen-cilag international n.v.    - recombinant modified vaccinia ankara bavarian nordic virus encoding the: ebola virus zaire (zebov) mayinga strain glycoprotein (gp); ebola virus sudan gulu strain gp; ebola virus taï forest strain nucleoprotein and the marburg virus musoke strain gp - verenvuotokuume ebola - rokotteet - active immunization for prevention of disease caused by ebola virus (zaire ebolavirus species) in individuals ≥ 1 year of age.

Suomi - suomi - Fimea (Suomen lääkevirasto)

bavarian nordic a/s - tick-borne encephalitis-virus (k23), kokovirus, inaktivoitu - injektioneste, suspensio - 0,75 mikrog / 0,25 ml - inaktivoitu puutiaisaivotulehdusrokote (koko virus)

Suomi - suomi - Fimea (Suomen lääkevirasto)

bavarian nordic a/s - tick-borne encephalitis-virus (k23), kokovirus, inaktivoitu - injektioneste, suspensio - 1,5 mikrog / 0,5 ml - inaktivoitu puutiaisaivotulehdusrokote (koko virus)

Euroopan unioni - suomi - EMA (European Medicines Agency)

bavarian nordic a/s - vibrio cholerae, kanta cvd-103-hgr, live - kolera - rokotteet - vaxchora is indicated for active immunisation against disease caused by vibrio cholerae serogroup o1 in adults and children aged 2 years and older. tätä rokotetta on käytettävä virallisten suositusten mukaisesti.

Euroopan unioni - suomi - EMA (European Medicines Agency)

dynavax gmbh - hepatiitti b-pinta-antigeeni - b-hepatiitti - rokotteet - heplisav b is indicated for the active immunisation against hepatitis b virus infection (hbv) caused by all known subtypes of hepatitis b virus in adults 18 years of age and older. the use of heplisav b should be in accordance with official recommendations. it can be expected that hepatitis d will also be prevented by immunisation with heplisav b as hepatitis d (caused by the delta agent) does not occur in the absence of hepatitis b infection.

Euroopan unioni - suomi - EMA (European Medicines Agency)

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.

Euroopan unioni - suomi - EMA (European Medicines Agency)

amgen technology (ireland) uc - bevasitsumabi - carcinoma, renal cell; peritoneal neoplasms; ovarian neoplasms; breast neoplasms; carcinoma, non-small-cell lung; fallopian tube neoplasms - antineoplastiset aineet - mvasi yhdessä fluoropyrimidiinipohjaisen kemoterapian kanssa on tarkoitettu hoidettaessa aikuispotilaita, joilla on metastasoitunut koolonin tai peräsuolen karsinooma. mvasi yhdessä paklitakselin kanssa on tarkoitettu ensilinjan hoito aikuisilla potilailla, joilla on metastasoitunut rintasyöpä. lisätietoja ihmisen epidermaalisen kasvutekijäreseptorin 2 (her2) tilasta on kohdassa 5. mvasi, lisäksi platina-pohjaista solunsalpaajahoitoa, on tarkoitettu käytettäväksi ensilinjan hoitoon aikuisille potilaille, joilla on leikattavissa oleva edennyttä, metastasoitunutta tai uusiutunutta ei-pienisoluista keuhkosyöpää muu kuin levyepiteelikarsinooma hallitsevana tyyppinä. mvasi in combination with interferon alfa-2a is indicated for first-line treatment of adult patients with advanced and/or metastatic renal cell cancer. mvasi, yhdessä karboplatiini-ja paklitakseli on tarkoitettu etulinjan hoito aikuisilla potilailla, joilla on pitkälle edennyt (international federation of naistentautien ja synnytysopin (figo) vaiheiden iiib, iiic ja iv) epiteliaalinen munasarjasyöpä, munanjohtimen, tai ensisijainen vatsakalvon syöpä. mvasi, yhdessä karboplatiinin ja gemsitabiinin tai yhdessä karboplatiini-ja paklitakseli on tarkoitettu aikuisille potilaille, joilla on ensimmäisen toistumisen platinum-herkkä epiteelin munasarjojen, munanjohtimien tai ensisijainen vatsakalvon syöpä, jotka eivät ole aiemmin saaneet hoitoa bevasitsumabilla tai muulla vegf-estäjien tai vegf-reseptorin kohdennettuja aineet. mvasi in combination with paclitaxel, 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. mvasi, yhdessä paklitakselin ja sisplatiinin tai vaihtoehtoisesti paklitakselin ja topotekaanin potilaille, jotka eivät voi saada platinum-hoito on tarkoitettu aikuisille potilaille, joilla on jatkuva, toistuva, tai metastasoitunut syöpä kohdunkaula.

Suomi - suomi - Fimea (Suomen lääkevirasto)

bayer ag - cocillanae poimia nestettä,noscapinum - imeskelytabletti - opiumjohdokset ja ekspektorantit, lukuun ottamatta mukolyyttejä

Suomi - suomi - Fimea (Suomen lääkevirasto)

stada arzneimittel ag stada arzneimittel ag - pregabalinum - kapseli, kova - 25 mg - pregabaliini