INTRAMAR DRY COW 600 mg Intramamární suspenze Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

intramar dry cow 600 mg intramamární suspenze

bioveta, a.s. - cloxacillin - intramamární suspenze - beta-laktamázy rezistentní peniciliny - dojnice v období stání na sucho

ORBENIN EXTRA DRY COW 600 mg Intramamární suspenze Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

orbenin extra dry cow 600 mg intramamární suspenze

zoetis Česká republika s.r.o. (2) - cloxacillin - intramamární suspenze - 600mg - beta-laktamázy rezistentní peniciliny - skot

Vectormune FP ILT + AE Evropská unie - čeština - EMA (European Medicines Agency)

vectormune fp ilt + ae

ceva-phylaxia co. ltd. - live recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus (rfp-lt) and avian encephalomyelitis virus, strain calnek 1143 (ae) - immunologicals for aves, live viral vaccines, domestic fowl - kuře - for active immunisation of chickens of 8 to 13 weeks of age in order to reduce the skin lesions due to fowlpox, to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis and to prevent egg production losses due to avian encephalomyelitis.

Vectormune FP ILT Evropská unie - čeština - EMA (European Medicines Agency)

vectormune fp ilt

ceva-phylaxia co. ltd. - recombinant fowlpox virus expressing the membrane fusion protein and the encapsidation protein of avian infectious laryngotracheitis virus, live - kuře - for active immunisation of chickens from 8 weeks of age in order to reduce the skin lesions due to fowlpox and to reduce the clinical signs and tracheal lesions due to avian infectious laryngotracheitis.

Librela Evropská unie - čeština - EMA (European Medicines Agency)

librela

zoetis belgium - bedinvetmab - analgetika - psi - for the alleviation of pain associated with osteoarthritis in dogs.

Solensia Evropská unie - čeština - EMA (European Medicines Agency)

solensia

zoetis belgium sa - frunevetmab - analgetika - kočky - for the alleviation of pain associated with osteoarthritis in cats.

Daxocox Evropská unie - čeština - EMA (European Medicines Agency)

daxocox

ecuphar nv - enflicoxib - produkty protizánětlivé a antirevmatické - psi - for the treatment of pain and inflammation associated with osteoarthritis (or degenerative joint disease) in dogs.

Rozlytrek Evropská unie - čeština - EMA (European Medicines Agency)

rozlytrek

roche registration gmbh  - entrectinib - cancer; carcinoma, non-small-cell lung - antineoplastická činidla - rozlytrek as monotherapy is indicated for the treatment of adult and paediatric patients 12 years of age and older with solid tumours expressing a neurotrophic tyrosine receptor kinase (ntrk) gene fusion,who have a disease that is locally advanced, metastatic or where surgical resection is likely to result in severe morbidity, andwho have not received a prior ntrk inhibitorwho have no satisfactory treatment options. rozlytrek as monotherapy is indicated for the treatment of adult patients with ros1 positive, advanced non small cell lung cancer (nsclc) not previously treated with ros1 inhibitors.

Brukinsa Evropská unie - čeština - EMA (European Medicines Agency)

brukinsa

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - antineoplastická činidla - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Palladia Evropská unie - čeština - EMA (European Medicines Agency)

palladia

zoetis belgium sa - toceranib - antineoplastická činidla - psi - léčba nádorů mastocytů, které nebyly resekatelné, patnaik stupeň ii (střední stupeň) nebo iii (recidivující kožní nádory žírných buněk) u psů.