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
 

Invirase and Fortovase (saquinavir) - confusion between two formulations: USA

United States of America. A problem with the HIV protease inhibitor saquinavir mesylate (Invirase) is its low bioavailability due to poor oral absorption and extensive first pass metabolism by the liver. This is such a drawback that the manufacturer of Invirase, Roche Laboratories, has reformulated the product as the free base and introduced it as Fortovase. The relative bioavailability is greater than 300% when saquinavir is administered as Fortovase compared with Invirase. However, Invirase remains on the market and is still used by some HIV-infected patients. The capsule size, 200 mg, is the same for both products.

Unfortunately, prescribing the drug by its generic name “saquinavir” has led to confusion between the two forms. A physician at a large community hospital prescribed saquinavir (Fortovase) 400 mg BID with food. The order was entered in the pharmacy computer as Fortovase (saquinavir) and the correct product was dispensed. However, on the following day, the pharmacy computer system noted “Fortovase 2 x 200 mg (saquinavir)”. Because Invirase is stored at room temperature, the technician preparing the patient’s medications found “saquinavir” in active unit dose stock as the Invirase product. The presence of Fortovase, which requires refrigeration, was completely overlooked and the Invirase product was dispensed in error. Fortunately, the nurse administering the medications noticed that the unit dose package listed Invirase instead of Fortovase and called the pharmacy before the patient got the wrong form of saquinavir.

To avoid repetition of this error, it is recommended to use both the brand and generic name when referring to these drugs. A special auxiliary label will be placed on each container to remind staff of the difference between the two products. Manufacturers are recommended to make minor adjustments in product strengths when there is this kind of potential for confusion between two products, e.g. providing Fortovase in a 175 mg dosage form instead of the same 200 mg strength as Invirase tablets would have greatly reduced error potential.

Reference: ISMP Medication Safety Alert! Vol. 3, Issue 13, 1 July 1998.

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Dernière mise à jour: le 3 mai 2013