A standing order under section 75 must include the following particulars:
(a) an approval number for the order that is different from the number given to each other standing order approved for the institution;
(b) the date of effect of the order and the date (not longer than 2 years after the date of effect) when the order ends;
(c) each ward to which the order applies;
(d) the clinical circumstances in which the medicine may be administered;
(e) a description of the people to whom the medicine may be administered;
(f) the medicine's approved name and, if applicable, brand name;
Note Approved name —see the medicines and poisons standard, par 1 (1).
(g) if applicable, the form and strength of the medicine;
(h) the dose and route of administration;
(i) if applicable, the frequency of administration.
Example—par (f) and par (g)
Adrenaline (EpiPen) 300 micrograms in 0.3mL pre-filled syringe
Note An
example is part of the regulation, is not exhaustive and may extend, but does
not limit, the meaning of the provision in which it appears (see Legislation
Act, s 126 and s 132).
Part 3.5 Medicines supply authorities
generally