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Injectafer® reçoit l'autorisation de la FDA américaine pour le traitement de l'anémie ferriprive

(PresseBox) (Bern, )
Injectafer® a reçu l'autorisation de l'autorité sanitaire américaine FDA (Food and Drug Adminis-tration) pour le traitement de l'anémie ferriprive. Le partenaire américain du Groupe Galenica, Luitpold Pharmaceuticals, Inc., va lancer immédiatement le médicament. Injectafer® sera produit sur le site de production de Luitpold à Columbus, Ohio.

Injectafer® (nom de marque de Ferinject® aux Etats-Unis, carboxymaltose ferrique) a reçu l'autorisation de la FDA américaine pour le traitement de l'anémie ferriprive chez les patients adultes réagissant de manière insuffisante au traitement par fer oral ou qui sont intolérants à celui-ci.

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