[26] These form the foundation for Table 2. Similar actions have been proposed by groups including the World Health Organization.[10] Lambert and colleagues argue that, since name similarity is easily and cheaply measured, steps should be taken to monitor and reduce similarity as a way to reduce the likelihood of drug name confusions to improve medication safety. This is sound advice, but difficult to implement on a national or international scale.[11] A number of organisations have produced broad strategies aimed at preventing drug confusion (JCAHO, ISMP and the US National Coordination Council for Medication Error Reporting).[12,14] There is considerable overlap with previously described strategies.

Additional recommendations include the unambiguous labelling of injectable and IV drug containers, and proposing that all prescriptions clearly specify medication click here strength, dosage, route of administration and frequency, even where there is only one accepted option. Finally, there is a strong endorsement for collaboration among all stakeholders to facilitate the design of packaging and labelling that minimises error. In addition to the actions proposed in Table 2, further processes recommended to reduce problems for pharmacists to use with error-associated

medications[29] include keeping patient medication profiles current, with sufficient information for pharmacists to evaluate the appropriateness 17-AAG ic50 of medication orders, reading product labels at least three times (e.g., when a product is selected, packaged and returned to the shelf) and counselling patients in order to provide an opportunity to ensure that an order has been dispensed correctly and that the patient understands the proper use of the medication.[29] Finally, a medication safety issue brief for hospitals and health networks[25] suggests

that actions to reduce errors from look-alike, sound-alike drugs should include organisations evaluating their formularies to identify medications that are prone to name confusion and Tangeritin that errors involving look-alike, sound-alike drugs are tracked, with the results used to educate staff. They also suggest providing drug name spelling with verbal orders, providing the intended use of the drug with the order, and conducting a ‘failure mode and effects analysis’ for all drugs being considered for inclusion on a formulary. Obstacles to changing names, labels or packages include: the nature of the problem; that standards for names, labels and packages do not incorporate human factors principles; and that most of the information on labelling and packaging problems is not systematic and comprehensive. There is also a barrier in the regulatory structure governing pharmaceuticals. Regulatory agencies do not yet ‘own’ the problem – they do not see it falling into their jurisdiction.