Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - lorlatinibum - compresse rivestite con film - lorlatinibum 25 mg, cellulosum microcristallinum, calcii hydrogenophosphas dihydricus, carboxymethylamylum natricum a corresp. natrium 0.315 mg, magnesii stearas, Überzug: hypromellosum, lactosum monohydricum 1.575 mg, macrogolum 4000, triacetinum, e 171, e 172 (nigrum), e 172 (rubrum), pro compresso obducto. - non a piccole cellule del polmone (non small cell lung cancer, nsclc) - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

pfizer ag - lorlatinibum - compresse rivestite con film - lorlatinibum 100 mg, cellulosum microcristallinum, calcii hydrogenophosphas dihydricus, carboxymethylamylum natricum a corresp. natrium 0.84 mg, magnesii stearas, Überzug: hypromellosum, lactosum monohydricum 4.2 mg, macrogolum 4000, triacetinum, e 171, e 172 (nigrum), e 172 (rubrum), pro compresso obducto. - non a piccole cellule del polmone (non small cell lung cancer, nsclc) - synthetika

Unione Europea - italiano - EMA (European Medicines Agency)

pfizer europe ma eeig - lorlatinib - carcinoma, polmone non a piccole cellule - 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.

Unione Europea - italiano - EMA (European Medicines Agency)

stemline therapeutics b.v. - elacestrant - neoplasie al seno - terapia endocrina - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

sandoz pharmaceuticals ag - erlotinibum - compresse rivestite con film - erlotinibum 25 mg ut erlotinibi hydrochloridum, lactosum monohydricum 23.98 mg, cellulosum microcristallinum, carboxymethylamylum natricum a, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, acidi methacrylici copolymerum a, natrii hydrogenocarbonas, e 171, pro compresso obducto corresp. natrium 0.2 mg. - onkologikum - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

sandoz pharmaceuticals ag - erlotinibum - compresse rivestite con film - erlotinibum 100 mg ut erlotinibi hydrochloridum, lactosum monohydricum 95.93 mg, cellulosum microcristallinum, carboxymethylamylum natricum a, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, acidi methacrylici copolymerum a, natrii hydrogenocarbonas, e 171, pro compresso obducto corresp. natrium 0.7 mg. - onkologikum - synthetika

Svizzera - italiano - Swissmedic (Swiss Agency for Therapeutic Products)

sandoz pharmaceuticals ag - erlotinibum - compresse rivestite con film - erlotinibum 150 mg ut erlotinibi hydrochloridum, lactosum monohydricum 143.9 mg, cellulosum microcristallinum, carboxymethylamylum natricum a, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, acidi methacrylici copolymerum a, natrii hydrogenocarbonas, e 171, pro compresso obducto corresp. natrium 1.1 mg. - onkologikum - synthetika

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

mylan s.p.a. - erlotinib - erlotinib

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

sun pharmaceutical industries (europe) b.v. - erlotinib - erlotinib

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

sandoz s.p.a. - erlotinib - erlotinib