The United Kingdom Misuse of Drugs Act 1971 aimed to control the possession and supply of numerous listed drugs and drug-like substances. The act allowed and regulated the use of some Controlled Drugs (designated CD) by various classes of persons (e.g. doctors) acting in their professional capacity.
In clinical practice, this mostly applies to the use of strong opiates for pain management and some amphetamine-like stimulants used for Attention-deficit hyperactivity disorder; both of which are regulated under Schedule 2.
The prescriber is responsible to minimise the risk of dependence or misuse by ensuring that such drugs are not started for a particular patient without good cause, that the dose is not increased to the point where dependency is more likely, and to avoid being an unwitting source of supply for addicts. The quantities of controlled drugs prescribed should match the likely needs of the patients until the next clinical review and prescription forms should be secured against theft.
The safe custody requirements ensures that doctors holding stock of controlled drugs must store them in securely fixed locked containers and maintain a written register. Disposal of expired stock must be witnessed by a designated inspector (either a local drug-enforcement police officer or official from health authority).
Pharmacologic agents | British laws | British Misuse of Drugs Act | Drug control law
This article is licensed under the GNU Free Documentation License.
It uses material from the
"Controlled Drug".
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