{"id":101062,"date":"2025-08-25T11:45:50","date_gmt":"2025-08-25T11:45:50","guid":{"rendered":"https:\/\/www.mymsd.ch\/fr\/?page_id=101062"},"modified":"2026-02-04T09:35:54","modified_gmt":"2026-02-04T09:35:54","slug":"isentress","status":"publish","type":"page","link":"https:\/\/www.mymsd.ch\/fr\/succinctstatement\/isentress\/","title":{"rendered":"Information professionnelle abr\u00e9g\u00e9e d\u2019Isentress\u00ae (Raltegravir)"},"content":{"rendered":"\n<h1 class=\"wp-block-heading has-border-color has-has-red-border-color-border-color  mhh-mcn-v1-heading mhh-mcn-v1-heading--92c407b7a83190cc88961398862a53d7\"><mark class=\"has-inline-color has-teal-500-color\">Information professionnelle abr\u00e9g\u00e9e d\u2019Isentress\u00ae (Raltegravir)<\/mark><\/h1>\n\n\n\n<p class=\"has-border-color has-has-red-border-color-border-color   mhh-mcn-v1-paragraph mhh-mcn-v1-paragraph--0e9efcd39b38350a80cceb81476dbf50\"><strong>ISENTRESS\u00ae (Raltegravir): PA: <\/strong>Raltegravir. <strong>I:<\/strong> Pour le traitement de l&rsquo;infection par le virus de l&rsquo;immunod\u00e9ficience humaine (VIH-1), en association avec des m\u00e9dicaments antir\u00e9troviraux.<strong> Po: <\/strong><em>Adulte:<\/em> 600 mg: 1x par jour 1200 mg (2&#215;600 mg) chez les patients na\u00effs de traitement ou les patients pr\u00e9trait\u00e9s, stables sous 400 mg 2x par jour, sans \u00e9chec de traitement virologique ant\u00e9rieur et virologiquement supprim\u00e9s sous 400 mg 2x par jour pendant au moins 6 mois dans le cadre du traitement initial du VIH. 400 mg: 2x par jour chez les patients na\u00effs de traitement ou les patients pr\u00e9trait\u00e9s. Les formulations ne sont pas bio\u00e9quivalentes, il ne faut donc pas substituer un comprim\u00e9 de 400 mg \u00e0 600 mg. <em>Enfants\/adolescents: <\/em>400 mg: 2x par jour si pc \u2265 25 kg. <em>Insuffisance r\u00e9nale: <\/em>Pas d&rsquo;adaptation de la dose. <em>Insuffisance l\u00e9g\u00e8re \u00e0 mod\u00e9r\u00e9e de la fonction h\u00e9patique:<\/em> Pas d&rsquo;adaptation de la dose. <strong>CI:<\/strong> Hypersensibilit\u00e9 aux ingr\u00e9dients. <strong>Pr:<\/strong> Le risque de transmission sexuelle du VIH ne peut \u00eatre exclu si le TAR prescrit n\u2019est pas pris r\u00e9guli\u00e8rement et\/ou si la suppression virologique n\u2019est pas atteinte et maintenue. <em>Co-infection<\/em> <em>par le VIH et le virus de l&rsquo;h\u00e9patite B (VHB) ou de l&rsquo;h\u00e9patite C (VHC)<\/em>: donn\u00e9es limit\u00e9es. <em>Ost\u00e9on\u00e9crose:<\/em> des cas ont \u00e9t\u00e9 rapport\u00e9s; consulter le m\u00e9decin en cas d\u2019apparition de sympt\u00f4mes, douleurs ou raideurs articulaires ou de difficult\u00e9s \u00e0 se mouvoir.<em> R\u00e9actions cutan\u00e9es graves et r\u00e9actions d&rsquo;hypersensibilit\u00e9: <\/em>R\u00e9actions cutan\u00e9es graves, potentiellement mortelles et fatales possibles en cas d&rsquo;utilisation concomitante avec des m\u00e9dicaments associ\u00e9s \u00e0 de telles r\u00e9actions (syndrome de Stevens-Johnson et n\u00e9crolyse \u00e9pidermique toxique) &#8211; l&rsquo;arr\u00eat imm\u00e9diat et un traitement ad\u00e9quat peuvent \u00eatre n\u00e9cessaires. <strong>IA:<\/strong> 400 mg: Attention aux inducteurs forts de l&rsquo;UGT1A1. 600 mg: la coadministration avec des inhibiteurs de l&rsquo;UGT1A1 et des inducteurs forts de l&rsquo;UGT1A1 n&rsquo;est pas recommand\u00e9e. Antiacides (contenant de l&rsquo;Al- et\/ou du Mg; et contenant du CaCO3 \u00e0 600 mg): l&rsquo;administration conjointe n&rsquo;est pas recommand\u00e9e. <strong>G\/A:<\/strong> 400 mg 2x par jour: Peut \u00eatre utilis\u00e9 pendant la grossesse si cliniquement necessaire; 600 mg: Aucune donn\u00e9:. donn\u00e9es limit\u00e9es. L&rsquo;allaitement maternel n&rsquo;est pas recommand\u00e9. <strong>EI: <\/strong>400 mg et 600 mg: fr\u00e9quence comparable des effets ind\u00e9sirables cliniques graves. Patients pr\u00e9trait\u00e9s: Li\u00e9es aux m\u00e9dicaments \u2265 2 %: diarrh\u00e9e, des c\u00e9phal\u00e9es. Patients n&rsquo;ayant jamais re\u00e7u de traitement: Li\u00e9es aux m\u00e9dicaments \u2265 2 %: Diarrh\u00e9e, naus\u00e9es, fatigue, vertiges, c\u00e9phal\u00e9es, insomnies, \u00e9ruption cutan\u00e9e, rash maculopapuleux .<strong> P: <\/strong>Flacons de 60: Comprim\u00e9s pellicul\u00e9s: 400 mg et 600 mg. <strong>CR:<\/strong> A. <strong>Td\u2019a<\/strong>: MSD Merck Sharp &amp; Dohme AG, Werftestrasse 4, 6005 Lucerne, Suisse. (V3.0); CH-MFA-00004.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-gray-300-color has-alpha-channel-opacity has-gray-300-background-color has-background\" \/>\n\n\n\n<p class=\"has-object-object-font-size has-border-color has-has-red-border-color-border-color   mhh-mcn-v1-paragraph mhh-mcn-v1-paragraph--ab167a8352f01bdeae9892af4daeda7a\"><em><mark class=\"has-inline-color has-gray-700-color\">Avant de prescrire, veuillez consulter l\u2019information professionnelle compl\u00e8te publi\u00e9e sur la page d&rsquo;accueil de Swissmedic (<a href=\"https:\/\/www.swissmedicinfo-pro.ch\/ShowText.aspx?textType=FI&amp;lang=FR&amp;authNr=58267\" target=\"_blank\" rel=\"noreferrer noopener\">www.swissmedicinfo-pro.ch<\/a>).<\/mark><\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Information professionnelle abr\u00e9g\u00e9e d\u2019Isentress\u00ae (Raltegravir) ISENTRESS\u00ae (Raltegravir): PA: Raltegravir. 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