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Modified-release opioid labelling — GPhC CRA MCQ

Instant feedback + full explanation. One question, done properly.

ModerateDispensing and SupplyModified-release opioid labellingGPhC CRA

A patient is prescribed modified-release oxycodone 10mg tablets twice daily and oxycodone oral solution for breakthrough pain. The dispensing label for the modified-release tablets says 'take when required for pain'. What is the legal classification/requirement?

Educational content. Not a substitute for clinical judgement or local policy.

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Correct answer: E — Correct the label to the regular modified-release dosing before supply.

Modified-release opioids are intended for regular dosing, while immediate-release preparations are used for breakthrough pain when prescribed. A 'when required' label on modified-release oxycodone could cause under-treatment, overuse or confusion. The label must be corrected and counselling provided.

Reference: BNF; MEP