{ "article": { "LEGIARTI000043175739": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "1", "ETAT": "VIGUEUR", "TYPE": "AUTONOME", "DATE_FIN": "2999-01-01", "DATE_DEBUT": "2021-05-24" } }, "META_COMMUN": { "ID": "LEGIARTI000043175739", "URL": "article/LEGI/ARTI/00/00/43/17/57/LEGIARTI000043175739.xml", "NATURE": "Article", "ORIGINE": "LEGI" } }, "LIENS": { "LIEN": [ { "@id": "LEGIARTI000006915537", "@num": "R5132-5", "#text": "Code de la santé publique - art. R5132-5 (M)", "@sens": "source", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" } ] }, "CONTEXTE": { "TEXTE": { "@cid": "JORFTEXT000043173376", "@nor": "SSAP2103145A", "@nature": "ARRETE", "TITRE_TXT": [ { "@fin": "2999-01-01", "#text": "Arrêté du 12 février 2021 portant application d'une partie de la réglementation des stupéfiants aux médicaments à base de prégabaline et fixant leur durée de prescription", "@debut": "2999-01-01", "@id_txt": "JORFTEXT000043173376", "@c_titre_court": "Arrêté du 12 février 2021" }, { "@fin": "2999-01-01", "#text": "Arrêté du 12 février 2021 portant application d'une partie de la réglementation des stupéfiants aux médicaments à base de prégabaline et fixant leur durée de prescription", "@debut": "2021-05-24", "@id_txt": "LEGITEXT000043175736", "@c_titre_court": "Arrêté du 12 février 2021" } ], "@ministere": "Ministère des solidarités et de la santé", "@date_publi": "2021-02-24", "@date_signature": "2021-02-12", "@num_parution_jo": "0047" } }, "VERSIONS": { "VERSION": [ { "@etat": "VIGUEUR", "LIEN_ART": { "@id": "LEGIARTI000043175739", "@fin": "2999-01-01", "@num": "1", "@etat": "VIGUEUR", "@debut": "2021-05-24", "@origine": "LEGI" } }, { "LIEN_ART": { "@id": "JORFARTI000043173379", "@fin": "2999-01-01", "@num": "1", "@debut": "2999-01-01", "@origine": "JORF" } } ] }, "BLOC_TEXTUEL": { "CONTENU": "

\n
Les médicaments à base de prégabaline sont soumis aux dispositions de l'article R. 5132-5 du code de la santé publique.

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La prescription ainsi que toute commande à usage professionnel de médicaments ou produits destinés à la médecine humaine ou de médicaments destinés à la médecine vétérinaire, classés comme stupéfiants ou soumis à la réglementation des stupéfiants est rédigée sur une ordonnance répondant à des spécifications techniques fixées, après avis du directeur général de l'Agence française de sécurité sanitaire des produits de santé, par arrêté du ministre chargé de la santé.
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" } }, "LEGIARTI000025787588": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "R5132-5", "ETAT": "MODIFIE", "TYPE": "AUTONOME", "DATE_FIN": "2023-12-22", "DATE_DEBUT": "2012-05-01" } }, "META_COMMUN": { "ID": "LEGIARTI000025787588", "URL": "article/LEGI/ARTI/00/00/25/78/75/LEGIARTI000025787588.xml", "NATURE": "Article", "ORIGINE": "LEGI" } }, "LIENS": { "LIEN": [ { "@id": "LEGIARTI000020796091", "@num": "1", "#text": "Arrêté du 31 mars 1999 - art. 1 (V)", "@sens": "cible", "@cidtexte": "JORFTEXT000000760590", "@nortexte": "MESP9921063A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "1999-03-31" }, { "@id": "JORFTEXT000000787339", "#text": "Décret n°2004-802 du 29 juillet 2004", "@sens": "source", "@cidtexte": "JORFTEXT000000787339", "@nortexte": "SANP0422530D", "@numtexte": "2004-802", "@typelien": "CODIFICATION", "@naturetexte": "DECRET", "@datesignatexte": "2004-07-29" }, { "@id": "LEGIARTI000028073853", "@num": "7", "#text": "Arrêté du 6 février 2009 - art. 7 (M)", "@sens": "cible", "@cidtexte": "JORFTEXT000020234297", "@nortexte": "SJSG0824493A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2009-02-06" }, { "@id": "LEGIARTI000023867032", "@num": "14", "#text": "Arrêté du 6 avril 2011 - art. 14 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000023865866", "@nortexte": "ETSH1109848A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2011-04-06" }, { "@id": "LEGIARTI000024536374", "@num": "1", "#text": "Arrêté du 24 août 2011 - art. 1 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000024535807", "@nortexte": "ETSP1123702A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2011-08-24" }, { "@id": "LEGIARTI000025541498", "@num": "2", "#text": "Arrêté du 9 mars 2012 - art. 2 (V)", "@sens": "cible", "@cidtexte": "JORFTEXT000025541141", "@nortexte": "ETSP1207340A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2012-03-09" }, { "@id": "LEGIARTI000025541500", "@num": "3", "#text": "Arrêté du 9 mars 2012 - art. 3 (V)", "@sens": "cible", "@cidtexte": "JORFTEXT000025541141", "@nortexte": "ETSP1207340A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2012-03-09" }, { "@id": "LEGIARTI000025767104", "@num": "1", "#text": "Arrêté du 16 avril 2012 - art. 1 (V)", "@sens": "cible", "@cidtexte": "JORFTEXT000025756650", "@nortexte": "ETSP1220641A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2012-04-16" }, { "@id": "LEGIARTI000025765496", "@num": "5", "#text": "Décret n°2012-597\n du 27 avril 2012 - art. 5", "@sens": "cible", "@cidtexte": "JORFTEXT000025757625", "@nortexte": "ETSP1206945D", "@numtexte": "2012-597", "@typelien": "MODIFIE", "@naturetexte": "DECRET", "@datesignatexte": "2012-04-27" }, { "@id": "LEGIARTI000026041155", "@num": "1", "#text": "Arrêté du 8 juin 2012 - art. 1 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000026040448", "@nortexte": "AFSP1225501A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2012-06-08" }, { "@id": "LEGIARTI000027200749", "@num": "2", "#text": "Arrêté du 12 mars 2013 - art. 2 (V)", "@sens": "cible", "@cidtexte": "JORFTEXT000027199914", "@nortexte": "AFSH1305477A", "@typelien": "CITATION", "@naturetexte": "ARRETE", "@datesignatexte": "2013-03-12" }, { "@id": "LEGIARTI000031143608", "#text": "ARRÊTÉ du 22 juillet 2015 - art. 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La prescription ainsi que toute commande à usage professionnel de médicaments ou produits destinés à la médecine humaine ou de médicaments destinés à la médecine vétérinaire, classés comme stupéfiants ou soumis à la réglementation des stupéfiants est rédigée sur une ordonnance répondant à des spécifications techniques fixées, après avis du directeur général de l'Agence nationale de sécurité du médicament et des produits de santé, par arrêté du ministre chargé de la santé.

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Lorsque la prescription de médicaments ou de produits destinés à la médecine humaine classés comme stupéfiants ou soumis à la réglementation des stupéfiants ne peut s'effectuer de manière dématérialisée, le prescripteur établit sur papier une prescription répondant à des spécifications techniques fixées par arrêté du ministre chargé de la santé, pris après avis du directeur général de l'Agence nationale de sécurité du médicament et des produits de santé. Il mentionne alors sur l'ordonnance celui des motifs mentionnés à l'article R. 4073-2 justifiant que la prescription soit établie sur ce support.
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Toute commande à usage professionnel de médicaments ou produits destinés à la médecine humaine ainsi que toute commande ou prescription de médicaments destinés à la médecine vétérinaire, classés comme stupéfiants, ou soumis à la réglementation des stupéfiants est rédigée sur une ordonnance répondant à des spécifications techniques fixées par l'arrêté mentionné à l'alinéa précédent.

\n
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Article 1 AUTONOME VIGUEUR, en vigueur depuis le 24/05/2021 (Arrêté du 12 février 2021 portant application d'une partie de la réglementation des stupéfiants aux médicaments à base de prégabaline et fixant leur durée de prescription)