bimectin horse oral paste pasta til inntöku 18,7 mg/g
bimeda animal health limited - ivermectinum inn - pasta til inntöku - 18,7 mg/g
serevent (serevent diskos) innöndunarduft 50 míkróg/skammt
glaxosmithkline pharma a/s - salmeterolum xínafóat - innöndunarduft - 50 míkróg/skammt
eqvalan vet. pasta til inntöku 1,87 %
boehringer ingelheim animal health france scs - ivermectinum inn - pasta til inntöku - 1,87 %
flixotide (flixotide diskos) innöndunarduft 100 míkróg/skammt
glaxosmithkline pharma a/s - fluticasonum própíónat - innöndunarduft - 100 míkróg/skammt
flixotide (flixotide diskos) innöndunarduft 250 míkróg/skammt
glaxosmithkline pharma a/s - fluticasonum própíónat - innöndunarduft - 250 míkróg/skammt
flixotide (flixotide diskos) innöndunarduft 500 míkróg/skammt
glaxosmithkline pharma a/s* - fluticasonum própíónat - innöndunarduft - 500 míkróg/skammt
skyrizi
abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - Ónæmisbælandi lyf - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.
nuvaring leggangainnlegg 0,120 mg/0,015 mg/24 klst.
n.v. organon* - etonogestrelum inn; ethinylestradiolum inn - leggangainnlegg - 0,120 mg/0,015 mg/24 klst.
ventoline (ventolin diskos) innöndunarduft 200 míkróg/skammt
glaxosmithkline pharma a/s - salbutamolum súlfat - innöndunarduft - 200 míkróg/skammt
hiprabovis ibr marker live
laboratorios hipra s.a - lifa ge- tk- tvöfalt gen-eytt nautgripavirus tegund 1, stofn ceddel: 106,3-107,3 ccid50 - Ónæmisfræðilegar upplýsingar - nautgripir - fyrir virka bólusetningar af nautgripum frá þriggja mánaða aldur gegn nautgripum herpesvírusinn tegund 1 (bohv-1) til að draga úr klínískum merki um smitandi nautgripum barkabólgu (ibr) og sviði veira skilst. upphaf ónæmis: 21 dagar eftir að grunnbólusetningarkerfið er lokið. lengd ónæmis: 6 mánuðum eftir að grunnbólusetningarkerfið er lokið.