BMJ  2005;331:456 (20 August), doi:10.1136/bmj.331.7514.456

Letter

Audit is important part of drug safety and regulation

The first 150 words of the full text of this article appear below.

EDITOR—Waller et al write about the responsibilities of the pharmaceutical companies and the regulating agencies such as the UK Medicines and Healthcare products Regulatory Agency to improve the safety of the drugs that are licensed for prescription.1 Although cyclo-oxygenase 2 inhibitors and selective serotonin reuptake inhibitors have been under the spotlight in recent months, other drugs may be of greater concern.

In 2000 the National Institute for Health and Clinical Excellence (NICE) issued guidance on the use of proton pump inhibitors in treating dyspepsia.2 In January 2005 in our hospital, an audit of record of 50 deceased patients identified 20 who were taking these drugs. Twelve of the 50 patients had had Clostridium difficile isolated in recent months, and eight of them had been taking proton pump inhibitors. Forty three patients received one or more antibiotics, 29 received three or more (cephalosporins 27, co-amoxiclav 19, metronidazole 19, clarithromycin . . . [Full text of this article]

Michael I Carter, consultant anaesthetist

Michael.Carter@ldh-tr.anglox.nhs.uk
Luton and Dunstable Hospital NHS Trust, Luton LU4 0DZ

Jane Murkin, patient safety manager

Luton and Dunstable Hospital NHS Trust, Luton LU4 0DZ


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Relevant Article

Drug safety and regulation
Patrick C Waller, Stephen J W Evans, and Keith Beard
BMJ 2005 331: 4-5. [Extract] [Full Text] [PDF]




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