CHAPTER 6 The administration of drugs
Every year in Australia, almost 200 million prescriptions are dispensed — that is about 10 prescriptions per year per person. In any 2-week period, 69% of the population have taken at least one medication and 91% of older people will have taken medicines.1 It is estimated that around 140 000 hospital admissions each year are associated with problems with the use of medicines. Medication error has been estimated to result in at least 80 000 hospital admissions and costs of at least $350 million per year.2 The great majority of medications that nurses administer on a day-to-day basis are considered to be, and are defined by legislation as, poisons. That is, generally speaking, they are substances that, by their very nature, are inherently dangerous to one’s health. Accordingly, it is considered necessary to identify them and then lay down clear provisions as to how such substances may be obtained, the basis on which a person may have possession of them, who may prescribe them, how they must be stored and so on. That process is undertaken by specific legislation.
The Commonwealth as well as each state and territory of Australia has specific legislation which covers the control and supply of poisons and therapeutic goods in that state or territory.3 Amongst other things, that legislation sets out the specific responsibilities of registered nurses in relation to the various types of drugs that they have to deal with and administer in their work. The possibility of drug errors, and the legal consequences that can flow from this, are such that nurses need to be aware not only of specific legislative requirements that apply to them, but also how to minimise the possibility of errors occurring.
The legislation referred to, known in New South Wales as the Poisons and Therapeutic Goods Act 1966, with a similar or like title in the other states and territories, does not deal only with the control of drugs in hospitals. Such legislation embraces all conceivable types of poisons available, ranging from agricultural poisons and domestic pesticides to drugs of addiction. The relevant legislation in each state and territory is relatively similar in the way in which it classifies and identifies poisons and therapeutic goods but there are differences in the detailed provisions that apply in some areas. In addition, as part of the legislation, certain criminal offences are indicated where a person deals with certain poisons, particularly the drugs of addiction, contrary to the provisions of the Act. It should be noted at this point that criminal charges in relation to well-publicised drug offences, such as possession or supply of heroin or cocaine, arise under other legislation. For example, in New South Wales such offences arise under the Drug Misuse and Trafficking Act 1985.
Substances which are for therapeutic use and:
Schedule 4 (Restricted Substances)
Substances which in the public interest should be supplied only by a medical practitioner, authorised nurse practitioner, dentist or veterinary surgeon, or by a pharmacist on the written prescription of a medical practitioner, authorised nurse practitioner, dentist or veterinary surgeon.
Substances of exceptional danger which require special precautions in their manufacture
Schedule 8 (Drugs of Addiction)
The legislation relating to poisons can be confusing if the relationship between the Act, the Regulations and the Poisons List or schedules is not readily understood. It can be easily understood by reference to Table 6.1, which explains how the legislative requirements complement each other in setting out specific provisions in each part.
POISONS ACT | POISONS LIST OR SCHEDULES | POISONS REGULATIONS |
---|---|---|
Divides available poisons into specific schedules under broad headings as to type | Specifically identifies by generic the name the drugs or poisons that come under the different schedules | Spells out in detail requirements concerning such details as to the prescription, control, possession, storage, supply, and administration of drugs or poisons under the schedule headings in the Act |
Clearly the three parts, so to speak, of the overall legislative provisions have to be applied in a complementary way. For example, the obvious question that any person would ask on reading the Act that identifies poisons into broadly defined schedules would be to inquire what specific drugs or poisons fall within those broad headings. To ascertain that information it is necessary to look to the complementary provisions. Specific requirements concerning such matters as authority to prescribe, control, possession, storage, supply and administration of the various types of drugs or poisons under the schedule headings will not be found in the Act. Such requirements will be found in the Regulations which accompany the Act and which are always in a separate document. As far as nursing staff are concerned, it is the Regulations that are the most important part of any poisons legislation, as they spell out precisely what must be done and observed in relation to the various substances, defined as poisons, that they deal with in the course of their work.
Hospitals are automatically notified of relevant changes to the poisons legislation by the state or territory health departments, generally by way of departmental circulars. To the extent that they are relevant, such circulars should be acted upon where necessary and distributed to all staff concerned.