Evropská unie - čeština - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Evropská unie - čeština - EMA (European Medicines Agency)

bial portela & companhia s.a. - opicapone - parkinsonova choroba - antiparkinsonické léky - ontilyv is indicated as adjunctive therapy to preparations of levodopa/ dopa decarboxylase inhibitors (ddci) in adult patients with parkinson’s disease and end-of-dose motor fluctuations who cannot be stabilised on those combinations.

Evropská unie - čeština - EMA (European Medicines Agency)

novartis europharm limited - nepafenac - pain, postoperative; ophthalmologic surgical procedures - oftalmologické látky - nevanac is indicated for: , prevention and treatment of postoperative pain and inflammation associated with cataract surgery;, reduction in the risk of postoperative macular oedema associated with cataract surgery in diabetic patients.

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

litcon pharma se, praha 8 array - 9125 dienogest; 578 ethinylestradiol - potahovaná tableta - 2mg/0,03mg - dienogest a ethinylestradiol

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

bayer ag, leverkusen array - 5388 nimodipin - potahovaná tableta - 30mg - nimodipin

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

bayer ag, leverkusen array - 2141 cyproteron-acetÁt - tableta - 100mg - cyproteron

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

bayer ag, leverkusen array - 2141 cyproteron-acetÁt - injekční roztok - 300mg - cyproteron

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

bayer ag, leverkusen array - 12 kyselina acetylsalicylovÁ - enterosolventní tableta - 100mg - kyselina acetylsalicylovÁ

Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

lallemand sas, blagnac array - 807 lactobacillus helveticus; 812 lacticaseibacillus rhamnosus - tvrdá tobolka - 2x10^9cfu - organismy produkujÍcÍ kyselinu mlÉČnou

Evropská unie - čeština - EMA (European Medicines Agency)

bayer ag - octocog alfa - hemofilie a - antihemoragika - léčba a profylaxe krvácení u pacientů s hemofilií a (vrozený nedostatek faktoru viii). iblias může být použit pro všechny věkové skupiny.