Marcain spinal Stungulyf, lausn 5 mg/ml أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain spinal stungulyf, lausn 5 mg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð - stungulyf, lausn - 5 mg/ml

Marcain spinal tung Stungulyf, lausn 5 mg/ml أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain spinal tung stungulyf, lausn 5 mg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð - stungulyf, lausn - 5 mg/ml

Marcain Stungulyf, lausn 2,5 mg/ml أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain stungulyf, lausn 2,5 mg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð - stungulyf, lausn - 2,5 mg/ml

Marcain Stungulyf, lausn 5 mg/ml أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain stungulyf, lausn 5 mg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð - stungulyf, lausn - 5 mg/ml

Marcain adrenalin Stungulyf, lausn 2,5 mg/ml+5 míkróg/m أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain adrenalin stungulyf, lausn 2,5 mg/ml+5 míkróg/m

aspen pharma trading limited - bupivacainum hýdróklóríð; adrenalinum bítartrat (epinephrinum bítartrat) - stungulyf, lausn - 2,5 mg/ml+5 míkróg/m

Marcain adrenalin Stungulyf, lausn 5 mg/ml+5 míkróg/ml أيسلندا - الأيسلاندية - LYFJASTOFNUN (Icelandic Medicines Agency)

marcain adrenalin stungulyf, lausn 5 mg/ml+5 míkróg/ml

aspen pharma trading limited - bupivacainum hýdróklóríð; adrenalinum bítartrat (epinephrinum bítartrat) - stungulyf, lausn - 5 mg/ml+5 míkróg/ml

Brukinsa الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

brukinsa

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - Æxlishemjandi lyf - 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).

Raplixa الاتحاد الأوروبي - الأيسلاندية - EMA (European Medicines Agency)

raplixa

mallinckrodt pharmaceuticals ireland limited - mannafíbrógen manna, trombín manna - hemostasis, skurðaðgerð - antihemorrhagics - stuðningsmeðferð þar sem venjulegar skurðaðgerðir eru ekki nægjanlegar til að bæta blóðflæði. raplixa verður að nota í ásamt samþykkt gelatín svampur. raplixa er ætlað í fullorðnir yfir 18 ára aldri.