Evrópusambandið - íslenska - EMA (European Medicines Agency)

eurogenerics holdings b.v. - teriparatíð - beinþynning - kalsíumsterastasis - qutavina is indicated in adults. meðferð við beinþynningu hjá konum eftir tíðahvörf og karlar við aukna hættu á beinbrotum. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. meðferð beinbrot tengslum við viðvarandi almenn sykurstera meðferð í konur og menn á jókst hættan fyrir beinbrot.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - Æxlishemjandi lyf - vegzelma in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. vegzelma in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. sjá nánar í kafla 5 til að fá nánari upplýsingar varðandi húðþéttni vaxtarþáttar viðtaka 2 (her2). vegzelma 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 vegzelma in combination with capecitabine. nánari upplýsingar um her2 stöðu, sjá kafla 5. vegzelma, 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 (nsclc) other than predominantly squamous cell histology. vegzelma, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent nsclc with epidermal growth factor receptor (egfr) activating mutations (see section 5. vegzelma, in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. vegzelma, 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. vegzelma, 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 vascular endothelial growth factor (vegf) inhibitors or vegf receptor–targeted agents. vegzelma 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 (see section 5. vegzelma, 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.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

roche registration gmbh - enfuvirtíð - hiv sýkingar - veirueyðandi lyf til almennrar notkunar - fuzeon er ætlað ásamt öðrum antiretroviral lyf til meðferð hiv-1-sýkt sjúklingar sem hafa fengið meðferð með og ekki á meðferð inniheldur að minnsta kosti einn lyf frá hvorri á eftir antiretroviral flokkum: próteasahemlar, ekki núkleósíð snúa-transcriptase hemlar og núkleósíð snúa-transcriptase hemla, eða sem hafa óþol fyrri antiretroviral meðferð. Í ákveða á ný meðferð fyrir sjúklinga sem hefur ekki tekist að antiretroviral meðferð, vandlega íhugun ætti að meðferð sögu sjúklingur og mynstur stökkbreytingar tengslum með mismunandi lyf. Þar sem í boði, viðnám prófa má viðeigandi.

Evrópusambandið - íslenska - EMA (European Medicines Agency)

eli lilly and company limited  - fentanýl - taugakerfi - hundar - til að stjórna verkjum í tengslum við hjálpartækjum og mjúkvefskurðaðgerð hjá hundum.

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

v.m.d. n.v. - butorphanolum tartrat - stungulyf, lausn - 10 mg/ml

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

elanco animal health gmbh - enrofloxacinum inn - stungulyf, lausn - 100 mg/ml

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

elanco animal health gmbh - enrofloxacinum inn - stungulyf, lausn - 50 mg/ml

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

norbrook laboratories (ireland) limited - amoxicillinum tríhýdrat; acidum clavulanicum kalíum - stungulyf, dreifa - 14,0/3,5 % w/v

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fatro s.p.a. - cloprostenolum natríum - stungulyf, lausn - 0,075 mg/ml

Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

laboratorios hipra s.a.* - ceftiofurum hýdróklóríð - stungulyf, dreifa - 50 mg/ml