US safety alert over Keppra and Kaletra
A safety alert concerning the potential for dispensing errors arising from confusion between Keppra (levetiracetam) and Kaletra (lopinavir and ritonavir) has been issued to US health care professionals by the Food and Drug Administration.
The FDA alert comes after it received four reports of confusion between
Keppra and Kaletra, one of which resulted in administration of the wrong
drug to a patient. “The similarities between the names, in addition
to the similarities in route of administration, dosage form and dosing
quantity may further increase the risk of confusion between Keppra and
Kaletra,” says the FDA.
FDA recommendations include:
Educating health care staff about the potential for medication errors
between these two products
Verifying all orders between pharmacists and prescribers by spelling
the proprietary name as well as the non-proprietary name
Including the indications with the prescription when ordering either
product
Using computerised alerts when prescriptions are processed, as well
as pharmacy shelf reminders
Kate Appleby, chief pharmacy technician for medicines management, Southern
Derbyshire Acute Hospitals NHS Trust, told The Journal that medication
errors arising from confusion between Keppra and Kaletra were not something
she had come across. “However, we do have problems with similar
named drugs.”
She explained that the trust was putting systems in place to ensure that
when drugs are purchased, a risk assessment is performed. “We look
at the packaging and drug name. We are also looking to assess where a
medicine will sit on pharmacy shelves to identify potential problems.”
A spokesman for the Medicines and Healthcare products Regulatory Agency
said that no yellow card reports of adverse events resulting from confusion
between these two products had been received in the UK.
Issues raised by a new report on medication errors are discussed in a
News feature on p80. |