Doksorubicin Accord 2 mg/ml koncentrat za raztopino za infundiranje Σλοβενία - Σλοβενικά - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

doksorubicin accord 2 mg/ml koncentrat za raztopino za infundiranje

accord healthcare - doksorubicin - koncentrat za raztopino za infundiranje - doksorubicin 1,88 mg / 1 ml - doksorubicin

Humira Ευρωπαϊκή Ένωση - Σλοβενικά - EMA (European Medicines Agency)

humira

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - imunosupresivi - prosimo, glejte dokument o izdelku.

Nulojix Ευρωπαϊκή Ένωση - Σλοβενικά - EMA (European Medicines Agency)

nulojix

bristol-myers squibb pharma eeig - belatacept - graft rejection; kidney transplantation - imunosupresivi - nulojix, in combination with corticosteroids and a mycophenolic acid (mpa), is indicated for prophylaxis of graft rejection in adult recipients of a renal transplant.

Berodual 0,5 mg/0,261 mg v 1 ml inhalacijska raztopina za nebulator Σλοβενία - Σλοβενικά - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

berodual 0,5 mg/0,261 mg v 1 ml inhalacijska raztopina za nebulator

boehringer ingelheim international gmbh - ipratropijev bromid; fenoterolijev bromid - inhalacijska raztopina za nebulator - ipratropijev bromid 0,25 mg / 1 ml  fenoterolijev bromid0,5 mg / 1 ml; fenoterolijev bromid 0,5 mg / 1 ml - fenoterol in ipratropijev bromid

Bovalto Ibraxion Ευρωπαϊκή Ένωση - Σλοβενικά - EMA (European Medicines Agency)

bovalto ibraxion

merial - inaktiviran virus ibr - imunologija za bovidae - govedo - aktivna imunizacija goveda za zmanjšanje kliničnih znakov kužnega govejega rinotraheitisa (ibr) in izločanja virusa na terenu. , nastop imunitete je 14 dni in trajanje imunosti je 6 mesecev.

Bovela Ευρωπαϊκή Ένωση - Σλοβενικά - EMA (European Medicines Agency)

bovela

boehringer ingelheim vetmedica gmbh - spremenjeno živo govedo virusne driske virus tipa 1, non-cytopathic staršev sev ke-9 in spremenjen živo govedo virusne driske virus tipa 2, ki niso cytopathic staršev sev ny-93 - immunologicals za bovidae, Živo virusna cepiva - za aktivno imunizacijo goveda (od 3 mesecev starosti za zmanjšanje hyperthermia in za zmanjšanje zmanjšanje leukocyte count zaradi goveja virusne driske virus (bvdv-1 in bvdv-2), in za zmanjšanje virus prelivanje in viraemia zaradi bvdv-2. za aktivno imunizacijo goveda proti bvdv-1 in bvdv-2, da se prepreči rojstvo vztrajno okuženih teleta, ki jih povzročajo okužbe transplacental.

Coxevac Ευρωπαϊκή Ένωση - Σλοβενικά - EMA (European Medicines Agency)

coxevac

ceva santé animale - inaktivirana cepiva coxiella burnetii, sev devet milj - immunologicals for bovidae, inactivated bacterial vaccines (including mycoplasma, toxoid and chlamydia) - goats; cattle - cattle: , for the active immunisation of cattle to lower the risk for non-infected animals vaccinated when non-pregnant to become shedder (5 times lower probability in comparison with animals receiving a placebo), and to reduce shedding of coxiella burnetii in these animals via milk and vaginal mucus. , onset of immunity: not established. , duration of immunity: 280 days after completion of the primary vaccination course. , goats: , for the active immunisation of goats to reduce abortion caused by coxiella burnetii and to reduce shedding of the organism via milk, vaginal mucus, faeces and placenta. , onset of immunity: not established. , duration of immunity: one year after completion of the primary vaccination course.

Letifend Ευρωπαϊκή Ένωση - Σλοβενικά - EMA (European Medicines Agency)

letifend

leti pharma, s.l.u. - recombinant protein q from leishmania infantum mon-1 - inaktivirano bakterijska cepiva (vključno z mikroplazma, toxoid in chlamydia) - psi - za aktivno imunizacijo psov od 6. meseca starosti, da zmanjšamo tveganje za nastanek kliničnega primera lizmanije.