Oyavas União Europeia - esloveno - 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 - antineoplastična sredstva - 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. za nadaljnje informacije o statusu receptorja človeškega epidermičnega rastnega faktorja 2 (her2) glejte poglavje 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. za nadaljnje informacije o statusu her2 glejte poglavje 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.

Adynovi União Europeia - esloveno - EMA (European Medicines Agency)

adynovi

baxalta innovations gmbh - rurioctocog alfa pegol - hemofilija a - antihemoragije - zdravljenje in preventivo za krvavitev pri bolnikih 12 let in zgoraj z hemofilija a (prirojeno faktor viii pomanjkljivost).

Imrestor União Europeia - esloveno - EMA (European Medicines Agency)

imrestor

elanco gmbh - pegbovigrastim - colony stimulating factors, immunostimulants, zdravila z delovanjem na novotvorbe agenti - cattle (cows and heifers); cattle - kot pomoč v programu za črede zmanjšati tveganje za klinični mastitis v perifernih mlečnih kravah in telicah v 30 dneh po telitvi.

Stimufend União Europeia - esloveno - EMA (European Medicines Agency)

stimufend

fresenius kabi deutschland gmbh - pegfilgrastim - nevtropenija - immunostimulants, , colony stimulating factors - skrajšanje trajanja nevtropenija in pojavnost vročinskih nevtropenija pri odraslih bolnikih, zdravljenih s citotoksično kemoterapijo za malignosti (razen kronično mieloično levkemijo in mielodisplastični sindrom).

INFECTOSCAB 5 % krema Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

infectoscab 5 % krema

infectopharm arzneimittel gmbh - permetrin - krema - permetrin 50 mg / 1 g - permetrin

INFECTOSCAB 5 % krema Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

infectoscab 5 % krema

infectopharm arzneimittel gmbh - permetrin - krema - permetrin 50 mg / 1 g - permetrin

INFECTOSCAB 5 % krema Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

infectoscab 5 % krema

infectopharm arzneimittel gmbh - permetrin - krema - permetrin 50 mg / 1 g - permetrin

INFECTOSCAB 5 % krema Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

infectoscab 5 % krema

infectopharm arzneimittel gmbh - permetrin - krema - permetrin 50 mg / 1 g - permetrin

INFECTOSCAB 5 % krema Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

infectoscab 5 % krema

infectopharm arzneimittel gmbh - permetrin - krema - permetrin 50 mg / 1 g - permetrin

INFECTOSCAB 5 % krema Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

infectoscab 5 % krema

infectopharm arzneimittel gmbh - permetrin - krema - permetrin 50 mg / 1 g - permetrin