(1) In this section
—
Schedule 4 poison and Schedule 8 poison have the
meanings given in the Medicines and Poisons Act 2014 section 3.
(2) The coordinating
practitioner for a patient who has made a self-administration decision must,
before prescribing a voluntary assisted dying substance for the patient,
inform the patient, in writing, of the following —
(a) the
Schedule 4 poison or Schedule 8 poison, or combination of those poisons,
constituting the substance;
(b) that
the patient is not under any obligation to obtain the substance;
(c) that
the patient is not under any obligation to self-administer the substance;
(d) that
the substance must be stored in accordance with the information provided by
the authorised supplier who supplies the substance;
(e) how
to prepare and self-administer the substance;
(f) the
method by which the substance will be self-administered;
(g) the
expected effects of self-administration of the substance;
(h) the
period within which the patient is likely to die after self-administration of
the substance;
(i)
the potential risks of self-administration of the
substance;
(j)
that, if the patient decides not to self-administer the substance, their
contact person must give the substance to an authorised disposer for disposal;
(k)
that, if the patient dies, their contact person must give any unused or
remaining substance to an authorised disposer for disposal.
(3) The coordinating
practitioner for a patient who has made a practitioner administration decision
must, before prescribing a voluntary assisted dying substance for the patient,
inform the patient, in writing, of the following —
(a) the
Schedule 4 poison or Schedule 8 poison, or combination of those poisons,
constituting the substance;
(b) that
the patient is not under any obligation to have the substance administered;
(c) the
method by which the substance will be administered;
(d) the
expected effects of administration of the substance;
(e) the
period within which the patient is likely to die after administration of the
substance;
(f) the
potential risks of administration of the substance;
(g)
that, if the practitioner administration decision is made after the revocation
of a self-administration decision, the contact person for the patient must
give any prescribed substance received by the patient, the contact person or
an agent of the patient to an authorised disposer for disposal.