The White Paper addresses key points that manufacturers should consider when designing labels, including:
• Why mix-ups with injectable drugs occur
• Impact on patient safety
• Contributing factors
• Labeling considerations
Med Safety Board suggests that pharmaceutical manufacturers not only consider the recommendations presented in the White Paper, but also proactively evaluate their product labeling and packaging for other safety concerns by following US Food and Drug Administration guidance documents and based on lessons learned from events published by ISMP. We also encourage healthcare organizations to consider these other error-prone aspects of labeling and packaging when determining which products to purchase or add to their formulary.
Download a copy of A Call to Action: Pharmaceutical Manufacturers Must Ensure Injectable Medication Labels are Well-Differentiated to Prevent Patient Harm
Contact Med Safety Board to learn more about assessing product risks for safe use in the clinical environment and to speak with our experts. You can also call (267) 725-0063 for a Complimentary Discovery Call to discuss your potential risks and the solutions that we offer.
This white paper was prepared through a grant from Long Grove Pharmaceuticals, LLC.