Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

interchemie werken de adelaar eesti as - ketoprofen - injekční roztok - deriváty kyseliny propionové - skot, prasata, koně

Evropská unie - čeština - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - artritida, revmatoidní - imunosupresiva - rheumatoid arthritisrinvoq is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease-modifying anti-rheumatic drugs (dmards). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

interchemie werken de adelaar eesti as - vápník, kombinace s vitaminem d a / nebo jinými léky - infuzní roztok - vÁpnÍk - skot, ovce, prasata

Evropská unie - čeština - EMA (European Medicines Agency)

alfasigma s.p.a. - methylthioniniumchloridu - colorectal neoplasms; colonoscopy - other diagnostic agents - lumeblue is indicated as a diagnostic agent enhancing visualisation of colorectal lesions in adult patients undergoing screening or surveillance colonoscopy.

Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

interchemie werken de adelaar eesti as - xylazinu - injekční roztok - jiná hypnotika a sedativa - skot, koně, psi, kočky

Česká republika - čeština - USKVBL (Ústav Pro Státní Kontrolu Veterinárních Biopreparátů A Léčiv)

interchemie werken de adelaar eesti as - jiné minerální produkty, kombinace - injekční roztok - jiné minerální produkty - koně, skot, psi, kočky

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ge healthcare as, oslo array - 20889 gadoterÁt-meglumin - injekční roztok v předplněné injekční stříkačce - 0,5mmol/ml - kyselina gadoterovÁ

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

ge healthcare as, oslo array - 20889 gadoterÁt-meglumin - injekční roztok - 0,5mmol/ml - kyselina gadoterovÁ

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

as grindeks, riga array - 3207 lenalidomid s chloridem amonnÝm - tvrdá tobolka - 10mg - lenalidomid

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

as grindeks, riga array - 3207 lenalidomid s chloridem amonnÝm - tvrdá tobolka - 15mg - lenalidomid