Den europeiske union - norsk - EMA (European Medicines Agency)

pharmathen s.a. - memantinhydroklorid - alzheimers sykdom - psychoanaleptics, , andre anti-demens legemidler - behandling av pasienter med moderat til alvorlig alzheimers sykdom.

Norge - norsk - Statens legemiddelverk

boehringer ingelheim animal health denmark a/s - ivermektin - påhellingsvæske, oppløsning - 5 mg/ ml

Den europeiske union - norsk - 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.

Den europeiske union - norsk - EMA (European Medicines Agency)

mundipharma corporation (ireland) limited - nalokson hydrochloride dihydrat - opioid-relaterte lidelser - alle andre terapeutiske produkter - nyxoid er beregnet til umiddelbar administrasjon som akuttapi for kjent eller mistenkt opioid overdose som manifestert av respiratorisk og / eller sentralnervesystemet depresjon i både ikke-medisinske og helsetjenester. nyxoid is indicated in adults and adolescents aged 14 years and over. nyxoid is not a substitute for emergency medical care.

Norge - norsk - Statens legemiddelverk

orifarm as - eprinomektin - påhellingsvæske, oppløsning - 5 mg/ ml

Norge - norsk - Statens legemiddelverk

lantheus mi uk ltd. - bicisatdihydroklorid ad tc-99m bicisate - pulver og væske til injeksjonsvæske, oppløsning

Norge - norsk - Statens legemiddelverk

as kalceks - deksmedetomidinhydroklorid - konsentrat til infusjonsvæske, oppløsning - 100 mikrog/ ml

Norge - norsk - Statens legemiddelverk

poa pharma scandinavia ab - ciprofloksacinhydroklorid / fluocinolonacetonid - Øredråper, oppløsning - 3 mg/ ml / 0.25 mg/ ml

Norge - norsk - Statens legemiddelverk

orpha-devel handels und vertriebs gmbh - naloksonhydrokloriddihydrat - injeksjons-/infusjonsvæske, oppløsning - 0.4 mg/ ml