Lipancrea 8000 8 000 j.Ph. Eur. Lipazy Kapsułki Polska - polski - URPL (Urząd Rejestracji Produktów Leczniczych, Wyrobów Medycznych i Produktów Biobójczych)

lipancrea 8000 8 000 j.ph. eur. lipazy kapsułki

zakłady farmaceutyczne polpharma s.a. - pankreatyna + amylasum + lipasum + proteaza - kapsułki - 8 000 j.ph. eur. lipazy

Lorviqua Unia Europejska - polski - EMA (European Medicines Agency)

lorviqua

pfizer europe ma eeig - lorlatinib - rak, niedrobnokomórkowe płuca - 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.

Glybera Unia Europejska - polski - EMA (European Medicines Agency)

glybera

uniqure biopharma b.v.  - alipogene tiparvovec - hiperlipoproteinemia typu i - Środki modyfikujące poziom lipidów - glybera jest wskazana dla dorosłych pacjentów, u których zdiagnozowano rodzinny niedobór lipazy lipoproteinowej (lpld) i którzy cierpią na ciężkie lub wielokrotne ataki zapalenia trzustki pomimo ograniczeń tłuszczu żywieniowego. rozpoznanie lpld musi być potwierdzone badaniami genetycznymi. wskazanie jest ograniczone do pacjentów z wykrywalnymi poziomami białka lpl.

Iclusig Unia Europejska - polski - EMA (European Medicines Agency)

iclusig

incyte biosciences distribution b.v. - ponatinib - leukemia, myeloid; leukemia, lymphoid - antineoplastic agents, protein kinase inhibitors - iclusig is indicated in adult patients withchronic phase, accelerated phase, or blast phase chronic myeloid leukaemia (cml) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutationphiladelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the t315i mutation. zobacz rozdziały 4. 2 assessment of cardiovascular status prior to start of therapy and 4. 4 situations where an alternative treatment may be considered.

Alunbrig Unia Europejska - polski - EMA (European Medicines Agency)

alunbrig

takeda pharma a/s - brigatinib - rak, niedrobnokomórkowe płuca - Środki przeciwnowotworowe - alunbrig is indicated as monotherapy 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. alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase alkpositive advanced nsclc previously treated with crizotinib.