Europska Unija - slovenski - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - pnevmokokne okužbe - cepiva - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. glej poglavja 4. 4 in 5. 1 za informacije o zaščiti proti specifičnim pnevmokoknim serotipom. apexxnar should be used in accordance with official recommendations. .

Europska Unija - slovenski - 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 - antineoplastična sredstva - 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. za nadaljnje informacije o statusu receptorja človeškega epidermičnega rastnega faktorja 2 (her2) glejte poglavje 5. 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. za nadaljnje informacije o statusu her2 glejte poglavje 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.

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

virbac 1ére avenue 2065 lid 06516 carros francija za vse nadaljnje informacije tem zdravilu se obrnite na lokalno predstavništvo imetnika dovoljenja za promet zdravilom -

Europska Unija - slovenski - EMA (European Medicines Agency)

gilead sciences ireland uc - bictegravir, emtricitabine, tenofovir alafenamide, fumarate - okužbe z virusom hiv - antivirusi za sistemsko uporabo - biktarvy is indicated for the treatment of human immunodeficiency virus 1 (hiv 1) infection in adults and paediatric patients at least 2 years of age and weighing at least 14 kg i without present or past evidence of viral resistance to the integrase inhibitor class, emtricitabine or tenofovir. (glejte poglavje 5).

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

merck d.o.o. - natrijev levotiroksinat - tableta - natrijev levotiroksinat 100 µg / 1 tableta - natrijev levotiroksinat

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

merck d.o.o. - natrijev levotiroksinat - tableta - natrijev levotiroksinat 150 µg / 1 tableta - natrijev levotiroksinat

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

merck d.o.o. - natrijev levotiroksinat - tableta - natrijev levotiroksinat 50 µg / 1 tableta - natrijev levotiroksinat

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

merck d.o.o. - natrijev levotiroksinat - tableta - natrijev levotiroksinat 25 µg / 1 tableta - natrijev levotiroksinat

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

lek d.d. - amoksicilin, klavulanska kislina - filmsko obložena tableta - amoksicilin 875 mg / 1 tableta amoksicilin trihidrat; klavulanska kislina 125 mg / 1 tableta kalijev klavulanat - amoksicilin in zaviralec laktamaz beta

Slovenija - slovenski - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

zaklady farmaceutyczne polfa lodz sa - pantoprazol - gastrorezistentna tableta - pantoprazol 20 mg / 1 tableta - pantoprazol