Locoid 0.1 % Norge - norsk - Statens legemiddelverk

locoid 0.1 %

cheplapharm arzneimittel gmbh - hydrokortisonbutyrat - salve - 0.1 %

Locoid Crelo 0.1 % w/w Norge - norsk - Statens legemiddelverk

locoid crelo 0.1 % w/w

cheplapharm arzneimittel gmbh - hydrokortisonbutyrat - liniment, emulsjon - 0.1 % w/w

Locoid Lipid 0.1 % Norge - norsk - Statens legemiddelverk

locoid lipid 0.1 %

cheplapharm arzneimittel gmbh - hydrokortisonbutyrat - krem - 0.1 %

Oyavas Den europeiske union - norsk - EMA (European Medicines Agency)

oyavas

stada arzneimittel ag - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastiske midler - 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. for ytterligere informasjon om human epidermal growth factor receptor 2 (her2) status, se avsnitt 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. for ytterligere informasjon om her2-status, se avsnitt 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.

Atacand Plus 16 mg / 12.5 mg Norge - norsk - Statens legemiddelverk

atacand plus 16 mg / 12.5 mg

cheplapharm arzneimittel gmbh - kandesartancileksetil / hydroklortiazid - tablett - 16 mg / 12.5 mg

Atacand Plus Mite 8 mg / 12.5 mg Norge - norsk - Statens legemiddelverk

atacand plus mite 8 mg / 12.5 mg

cheplapharm arzneimittel gmbh - kandesartancileksetil / hydroklortiazid - tablett - 8 mg / 12.5 mg

Atacand Plus 32 mg / 12.5 mg Norge - norsk - Statens legemiddelverk

atacand plus 32 mg / 12.5 mg

cheplapharm arzneimittel gmbh - kandesartancileksetil / hydroklortiazid - tablett - 32 mg / 12.5 mg

Lariam 250 mg Norge - norsk - Statens legemiddelverk

lariam 250 mg

cheplapharm arzneimittel gmbh - meflokinhydroklorid - tablett - 250 mg

Icatibant Glenmark 30 mg Norge - norsk - Statens legemiddelverk

icatibant glenmark 30 mg

glenmark arzneimittel gmbh - ikatibantacetat - injeksjonsvæske, oppløsning i ferdigfylt sprøyte - 30 mg

Dimethyl fumarate Glenmark 240 mg Norge - norsk - Statens legemiddelverk

dimethyl fumarate glenmark 240 mg

glenmark arzneimittel gmbh - dimetylfumarat - enterokapsel, hard - 240 mg