Oyavas Union européenne - français - 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 - agents antinéoplasiques - 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. pour plus d'informations sur le statut du récepteur du facteur de croissance épidermique humain 2 (her2), veuillez vous référer à la section 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. pour plus d'informations sur le statut her2, veuillez vous référer à la section 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.

Sogroya Union européenne - français - EMA (European Medicines Agency)

sogroya

novo nordisk a/s - somapacitan - croissance - hormones hypophysaires et hypothalamiques et analogues - sogroya is indicated for the replacement of endogenous growth hormone (gh) in children  aged 3  years and above, and adolescents with growth failure due to growth hormone deficiency (paediatric ghd), and in adults with growth hormone deficiency (adult ghd).

Oyavas 100 mg/4 ml Solution à diluer pour Perfusion Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

oyavas 100 mg/4 ml solution à diluer pour perfusion

spirig healthcare ag - bevacizumabum - solution à diluer pour perfusion - bevacizumabum 100 mg, trehalosum dihydricum, natrii dihydrogenophosphas monohydricus, dinatrii phosphas, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 4 ml corresp. natrium 5.42 mg. - metastasiertes kolon- oder rektumkarzinom, metastasiertes mammakarzinom, fortgeschrittenes, metastasiertes oder rezidivierendes nicht-kleinzelliges lungenkarzinom (nsclc), fortgeschrittenes und/oder metastasierendes nierenzellkarzinom, glioblastom (who grad iv), ovarialkarzinom, zervixkarzinom - biotechnologika

Oyavas 400 mg/16 ml Solution à diluer pour Perfusion Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

oyavas 400 mg/16 ml solution à diluer pour perfusion

spirig healthcare ag - bevacizumabum - solution à diluer pour perfusion - bevacizumabum 400 mg, trehalosum dihydricum, natrii dihydrogenophosphas monohydricus, dinatrii phosphas, polysorbatum 20, aqua ad iniectabile q.s. ad solutionem pro 16 ml corresp. natrium 21.68 mg. - metastasiertes kolon- oder rektumkarzinom, metastasiertes mammakarzinom, fortgeschrittenes, metastasiertes oder rezidivierendes nicht-kleinzelliges lungenkarzinom (nsclc), fortgeschrittenes und/oder metastasierendes nierenzellkarzinom, glioblastom (who grad iv), ovarialkarzinom, zervixkarzinom - biotechnologika

SOGROYA Solution Canada - français - Health Canada

sogroya solution

novo nordisk canada inc - somapacitan - solution - 5mg - somapacitan 5mg

SOGROYA Solution Canada - français - Health Canada

sogroya solution

novo nordisk canada inc - somapacitan - solution - 10mg - somapacitan 10mg

SOGROYA Solution Canada - français - Health Canada

sogroya solution

novo nordisk canada inc - somapacitan - solution - 15mg - somapacitan 15mg