Home > PJ (current issue) > News / News Centre | Search

PJ Online homeThe Pharmaceutical Journal
Vol 280 No 7502 p586
17 May 2008

This article
Reprint   Photocopy

  Acrobat Reader


News summary


Design guide recommends simple changes to injectable medicines

Graphic designers from the Royal College of Art have helped develop new National Patient Safety Agency guidelines for the labelling and packaging of injectable medicines.

Label with dense text   Label that highlights key information

Dense text can be hard to read so the guide recommends creating an area that highlights key information and using appropriate fonts and formatting

The guidelines recommend simple changes in design, such as using paper labels and different coloured print, to help distinguish similar medicines from each other and prevent mistakes in administering the drugs.

The guidelines — “Design for patient safety: a guide to labelling and packaging of injectables” — apply to all injectable medicines, including ampoules, vials, prefilled syringes and infusion bags.

The NPSA recommends creating an area on a vial — no wider than the container’s width — that incorporates key information and ensures that the generic drug name can be read at a glance.

Where possible, labels on ampoules should be made of paper because text on transparent labels can show through on the reverse, making reading confusing, the guidelines suggest. Where ampoules do have clear plastic labels it may be better to highlight key information by inverting the text colour, the NPSA recommends.

The agency also proposes that a two-dimensional barcode that includes key information, such as batch number and expiry date, should appear on vial and infusion products. The barcode could also include a unique product identifier, to be used in the dispensing and medicine preparation process, as well as for administrative purposes.

The guidelines are the latest in a series around design and patient safety and are aimed at pharmaceutical companies as well as those involved in the procurement of NHS medicines.

They are also expected to help NHS trusts carry out a risk assessment of their injectable medicines and products following recommendations made by the NPSA last year (PJ, 7 April 2007, p392).

Back to Top


©The Pharmaceutical Journal