WHO Pharmaceuticals Newsletter 1998, No. 09&10
(1998; 23 pages)
Table des matières
Ouvrir ce répertoire et afficher son contenuRegulatory decisions
Ouvrir ce répertoire et afficher son contenuDrug surveillance
Ouvrir ce répertoire et afficher son contenuNew developments
Ouvrir ce répertoire et afficher son contenuMedical devices
Ouvrir ce répertoire et afficher son contenuGeneral information
Fermer ce répertoireMedication errors
Afficher le documentFlomax and Fosamax - name confusion: USA
Afficher le documentInvirase and Fortovase (saquinavir) - confusion between two formulations: USA
Afficher le documentLipid-based drug products - errors due to confusion with conventional products: USA
Afficher le documentMinimizing medical product errors - summary of workshop available: USA
Afficher le documentNeumega and Neupogen - name confusion: USA
Afficher le documentNortriptyline - errors in dosage: USA
Afficher le documentOxycodone - errors due to formulation confusion: USA
Afficher le documentSoriatane and Loxitane - prescribing errors due to name confusion: USA
Ouvrir ce répertoire et afficher son contenuVeterinary medicine
 

Soriatane and Loxitane - prescribing errors due to name confusion: USA

United States of America. The Food and Drug Administration and the United States Pharmacopeia have recently received reports noting confusion between Soriatane (acitretin) Capsules and Loxitane (loxapine) Capsules.

Soriatane is a retinoid that is indicated for severe psoriasis. Because of its teratogenic potential, Soriatane should be prescribed only by physicians who have special competence in the diagnosis and treatment of severe psoriasis, are experienced in the use of systemic retinoids, and understand the risk of teratogenicity.

Loxitane is indicated for the management of the manifestations of psychotic disorders. It has been available for a number of years and is currently also available generically. The confusion occurs because, when written, a cursive “S” and “L” and small “ri” and “xi” may look similar. The fact that the two products are available in the same two strengths (10 mg and 25 mg) and dosage form (capsule) has created the possibility for a serious dispensing error.

Reference: MedWatch - Important prescribing notice, September 1998 [http://www.fda.gov/medwatch/safety/1998/soriat.htm].

 

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Dernière mise à jour: le 3 mai 2013