Clopidogrel BMS Եվրոպական Միություն - չեխերեն - EMA (European Medicines Agency)

clopidogrel bms

bristol-myers squibb pharma eeig - clopidogrel (as hydrogen sulfate) - stroke; peripheral vascular diseases; myocardial infarction; acute coronary syndrome - antitrombotické činidla - klopidogrel je indikován u dospělých k prevenci aterotrombotických příhod u:- pacientů po infarktu myokardu (proběhlém před několika dny až méně než před 35 dny), po ischemické cévní mozkové příhodě (od 7 dny až méně než před 6 měsíci) nebo prokázaným onemocněním periferních tepen. - u pacientů, kteří trpí akutní koronární syndrom bez st elevace akutní koronární syndrom (nestabilní angina pectoris nebo non-q infarkt myokardu), včetně pacientů, kteří podstoupili stentu po perkutánní koronární intervenci, v kombinaci s kyselinou acetylsalicylovou (asa). st elevace akutního infarktu myokardu, v kombinaci s asa u medikamentózně léčených pacientů vhodných pro trombolytickou terapii.

Enhertu Եվրոպական Միություն - չեխերեն - EMA (European Medicines Agency)

enhertu

daiichi sankyo europe gmbh - trastuzumab deruxtecan - neoplasmy prsů - antineoplastická činidla - breast cancerher2-positive breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-positive breast cancer who have received one or more prior anti-her2-based regimens. her2-low breast cancerenhertu as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic her2-low breast cancer who have received prior chemotherapy in the metastatic setting or developed disease recurrence during or within 6 months of completing adjuvant chemotherapy (see section 4. non-small cell lung cancer (nsclc)enhertu as monotherapy is indicated for the treatment of adult patients with advanced nsclc whose tumours have an activating her2 (erbb2) mutation and who require systemic therapy following platinum-based chemotherapy with or without immunotherapy. gastric cancerenhertu as monotherapy is indicated for the treatment of adult patients with advanced her2-positive gastric or gastroesophageal junction (gej) adenocarcinoma who have received a prior trastuzumab-based regimen.

Padcev Եվրոպական Միություն - չեխերեն - EMA (European Medicines Agency)

padcev

astellas pharma europe b.v. - enfortumab vedotin - carcinoma, transitional cell; urologic neoplasms - antineoplastická činidla - padcev as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic urothelial cancer who have previously received a platinum-containing chemotherapy and a programmed death receptor 1 or programmed death ligand 1 inhibitor.

AMBRISENTAN ZENTIVA 10MG Potahovaná tableta Չեխիա - չեխերեն - SUKL (Státní ústav pro kontrolu léčiv)

ambrisentan zentiva 10mg potahovaná tableta

zentiva, k.s., praha array - 16475 ambrisentan - potahovaná tableta - 10mg - ambrisentan

AMBRISENTAN ZENTIVA 5MG Potahovaná tableta Չեխիա - չեխերեն - SUKL (Státní ústav pro kontrolu léčiv)

ambrisentan zentiva 5mg potahovaná tableta

zentiva, k.s., praha array - 16475 ambrisentan - potahovaná tableta - 5mg - ambrisentan

Desloratadine ratiopharm Եվրոպական Միություն - չեխերեն - EMA (European Medicines Agency)

desloratadine ratiopharm

ratiopharm gmbh - desloratadin - rhinitis, allergic, perennial; urticaria; rhinitis, allergic, seasonal - antihistaminika pro systémové použití, - desloratadine ratiopharm is indicated in adults for the relief of symptoms associated with:allergic rhinitischronic idiopathic urticaria as initially diagnosed by a physician.

JANSITIN 100MG Potahovaná tableta Չեխիա - չեխերեն - SUKL (Státní ústav pro kontrolu léčiv)

jansitin 100mg potahovaná tableta

g.l. pharma gmbh, lannach array - 41 monohydrÁt sitagliptin-hydrochloridu - potahovaná tableta - 100mg - sitagliptin

JANSITIN 25MG Potahovaná tableta Չեխիա - չեխերեն - SUKL (Státní ústav pro kontrolu léčiv)

jansitin 25mg potahovaná tableta

g.l. pharma gmbh, lannach rakousko - 41 monohydrÁt sitagliptin-hydrochloridu - potahovaná tableta - 25mg - sitagliptin