sendoxan tafla 50 mg
baxter medical ab* - cyclophosphamidum inn - tafla - 50 mg
warfarin teva tafla 1 mg
teva b.v.* - warfarinum natríum - tafla - 1 mg
rimactan hart hylki 300 mg
sandoz gmbh* - rifampicinum inn - hart hylki - 300 mg
rimactan hart hylki 150 mg
sandoz gmbh* - rifampicinum inn - hart hylki - 150 mg
sendoxan stungulyfsstofn, lausn 1 g
baxter medical ab* - cyclophosphamidum inn - stungulyfsstofn, lausn - 1 g
sendoxan stungulyfsstofn, lausn 500 mg
baxter medical ab* - cyclophosphamidum inn - stungulyfsstofn, lausn - 500 mg
warfarin teva tafla 3 mg
teva b.v.* - warfarinum natríum - tafla - 3 mg
verzenios
eli lilly nederland b.v. - abemaciclib - brjóstakrabbamein - Æxlishemjandi lyf - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.
mitomycin medac duft og leysir fyrir þvagblöðrulausn 40 mg
medac gesellschaft für klinische spezialpräparate gmbh - mitomycinum inn - duft og leysir fyrir þvagblöðrulausn - 40 mg
conbriza
pfizer europe ma eeig - bazedoxífen - beinþynning, eftir tíðahvörf - hormón kynlíf og stillum kynfæri - conbriza er ætlað til meðferðar við beinþynningu eftir tíðahvörf hjá konum með aukna hættu á beinbrotum. verulegur fækkun á tíðni beinbrota hefur sýnt fram á að; verkun á mjaðmarbrotum hefur ekki verið staðfest. Þegar ákvörðun val á conbriza eða öðrum meðferð, þar á meðal estrógenum, fyrir einstaka tíðahvörf kona, skal íhuga að tíðahvörf einkenni, áhrif á legi og barn vefja, og hjarta áhættu og fríðindi.