Zinacef Stungulyfs-/innrennslisstofn, lausn 750 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

zinacef stungulyfs-/innrennslisstofn, lausn 750 mg

sandoz a/s - cefuroximum natríum - stungulyfs-/innrennslisstofn, lausn - 750 mg

Zinacef Stungulyfs-/innrennslisstofn, lausn 1,5 g Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

zinacef stungulyfs-/innrennslisstofn, lausn 1,5 g

sandoz a/s - cefuroximum natríum - stungulyfs-/innrennslisstofn, lausn - 1,5 g

Solu-Medrol Stungulyfsstofn og leysir, lausn 40 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

solu-medrol stungulyfsstofn og leysir, lausn 40 mg

pfizer aps - methylprednisolonum natríumsúkkínat - stungulyfsstofn og leysir, lausn - 40 mg

Solu-Cortef Stungulyfsstofn og leysir, lausn 100 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

solu-cortef stungulyfsstofn og leysir, lausn 100 mg

pfizer aps - hydrocortisonum natríumsúkkínat - stungulyfsstofn og leysir, lausn - 100 mg

Solu-Cortef Stungulyfsstofn og leysir, lausn 250 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

solu-cortef stungulyfsstofn og leysir, lausn 250 mg

pfizer aps - hydrocortisonum natríumsúkkínat - stungulyfsstofn og leysir, lausn - 250 mg

Solu-Medrol Stungulyfsstofn og leysir, lausn 125 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

solu-medrol stungulyfsstofn og leysir, lausn 125 mg

pfizer aps - methylprednisolonum natríumsúkkínat - stungulyfsstofn og leysir, lausn - 125 mg

Solu-Medrol Stungulyfsstofn og leysir, lausn 500 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

solu-medrol stungulyfsstofn og leysir, lausn 500 mg

pfizer aps - methylprednisolonum natríumsúkkínat - stungulyfsstofn og leysir, lausn - 500 mg

Lorviqua Evrópusambandið - íslenska - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - krabbamein, lungnakrabbamein - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Xalkori Evrópusambandið - íslenska - EMA (European Medicines Agency)

xalkori

pfizer europe ma eeig - crizotinib - krabbamein, lungnakrabbamein - Æxlishemjandi lyf - xalkori as monotherapy is indicated for:the first‑line treatment of adults with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with previously treated anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with ros1‑positive advanced non‑small cell lung cancer (nsclc)the treatment of paediatric patients (age ≥6 to.

Zykadia Evrópusambandið - íslenska - EMA (European Medicines Agency)

zykadia

novartis europharm limited - ceritinib - krabbamein, lungnakrabbamein - Æxlishemjandi lyf - zykadia er ætlað til meðferðar hjá fullorðnum sjúklingum með lungnakrabbamein (anaplastic lymphoma kinase (alk)) sem hefur áður fengið meðferð með crizotinibi.