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This act controls the manufacture, supply, possession and use of drugs that are dangerous or otherwise harmful. These drugs were known as dangerous drugs but are now referred to as controlled drugs. The use of controlled drugs for medicinal purposes is permitted by the Misuse of Drugs Regulations and subsequent amendments. The regulations define classes of people who are authorized to supply and possess controlled drugs during the course of their professional activities. Controlled drugs are divided into five Schedules by the Regulations.

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Side effects, which become common with high doses, are arrhythmia, hypotension, convulsions, nausea and vomiting, headache and insomnia. Drugs in this group are also known as mast-cell stabilizers and they probably work by blocking the release of mediators such as histamine and serotonin in the lung, although their exact mode of action is unknown. They can be used prophylactically to reduce the incidence of asthmatic attacks and to allow reduction in the doses of other drugs. They are not used in chronic bronchitis.

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Adverse effects are increase in appetite and weight gain, which is serious in already obese patients. Hypoglycaemia can occur with any of these drugs and is particularly dangerous in the elderly. Gastrointestinal upsets and allergic skin rashes have been reported, as has bone marrow damage, which is rare but nevertheless severe. Biguanides do not affect insulin production but they do require some functioning β-cells to work. They seem to increase glucose uptake by peripheral muscle cells and reduce gluconeogenesis and intestinal glucose absorption. Only one, metformin, is available in the United Kingdom.

Authored by Cherrylene Lindgren, DO


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The two should be able to communicate easily, share access to the same common patient record and any guidelines used in the CMP, agree common understanding of and access to the written CMP and ideally review the patients progress together at agreed intervals. The responsibilities of the independent prescriber are given below: Initial clinical assessment and diagnosis of the patient Agreement with the supplementary prescriber about the limits of their responsibility Provision of advice and support to the supplementary prescriber Review of patients progress at appropriate intervals with the supplementary prescriber if possible Sharing patients records with supplementary prescriber Reporting of adverse drug reactions.

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