Haldol Depot Stungulyf, lausn 100 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

haldol depot stungulyf, lausn 100 mg/ml

essential pharma limited - haloperidolum dekanóat - stungulyf, lausn - 100 mg/ml

Efexor Depot Hart forðahylki 150 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

efexor depot hart forðahylki 150 mg

upjohn eesv - venlafaxinum hýdróklóríð - hart forðahylki - 150 mg

Efexor Depot Hart forðahylki 75 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

efexor depot hart forðahylki 75 mg

upjohn eesv - venlafaxinum hýdróklóríð - hart forðahylki - 75 mg

Cisordinol Depot Stungulyf, lausn 200 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

cisordinol depot stungulyf, lausn 200 mg/ml

h. lundbeck a/s* - zuclopenthixolum decanóat - stungulyf, lausn - 200 mg/ml

Fluanxol Depot Stungulyf, lausn 20 mg/ml Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

fluanxol depot stungulyf, lausn 20 mg/ml

h. lundbeck a/s* - flupenthixolum dekanóat (cis) - stungulyf, lausn - 20 mg/ml

Madopar Depot Hart forðahylki 100 mg/25 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

madopar depot hart forðahylki 100 mg/25 mg

roche pharmaceuticals a/s - benserazidum hýdróklóríð; levodopum inn - hart forðahylki - 100 mg/25 mg

Clopidogrel HCS Evrópusambandið - íslenska - EMA (European Medicines Agency)

clopidogrel hcs

hcs bvba  - clopidogrel (as hydrochloride) - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - blóðþurrðandi lyf - efri fyrirbyggja atherothrombotic eventsclopidogrel er ætlað:fullorðinn sjúklingar sem þjáist af kransæðastíflu (frá nokkrum dögum fyrr en minna en 35 dögum), blóðþurrðar heilablóðfall (frá 7 daga þar til að minna en 6 mánuðum) eða komið útlæga slagæð sjúkdómur. fullorðinn sjúklingar sem þjáist af bráðu kransæðastíflu:ekki l hækkun bráð kransæðastíflu (óstöðug hálsbólgu eða ekki q-bylgja kransæðastíflu), þar á meðal sjúklinga gangast undir stoðneti staðsetningar eftir stungið kransæðastíflu afskipti, ásamt asetýlsalisýlsýru (asa). l hækkun, bráð myndun stíflufleygs, ásamt asa í læknisfræðilega sjúklingum rétt fyrir segaleysandi meðferð. fyrirbyggja atherothrombotic og bláæðum atburðum í gáttum fibrillationin fullorðinn sjúklinga með gáttum tif sem hafa minnsta kosti einn hættu þáttur í æðum viðburði, eru ekki við hæfi fyrir meðferð með c-k-mótlyf (vka) og sem hafa lágt blæðingar hættu, eða er ætlað ásamt asa til að fyrirbyggja atherothrombotic og bláæðum viðburði, þar á meðal heilablóðfall.  for further information please refer to section 5.

Zolsketil pegylated liposomal Evrópusambandið - íslenska - EMA (European Medicines Agency)

zolsketil pegylated liposomal

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.

Arikayce liposomal Evrópusambandið - íslenska - EMA (European Medicines Agency)

arikayce liposomal

insmed netherlands b.v. - amikacin sulfate - sýkingar í öndunarvegi - sýklalyf fyrir almenn nota, - arikayce liposomal is indicated for the treatment of non-tuberculous mycobacterial (ntm) lung infections caused by mycobacterium avium complex (mac) in adults with limited treatment options who do not have cystic fibrosis.

Seroquel Prolong Forðatafla 50 mg Ísland - íslenska - LYFJASTOFNUN (Icelandic Medicines Agency)

seroquel prolong forðatafla 50 mg

cheplapharm arzneimittel gmbh - quetiapinum fúmarat - forðatafla - 50 mg