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s 65

Information to be given before prescribing voluntary assisted dying substance

In force
Part 4Accessing voluntary assisted dying and death
Division 3Prescribing, supplying and disposing of voluntary assisted dying substance

65 Information to be given before prescribing voluntary assisted dying substance

(1)

The coordinating practitioner for a person who has made a self-administration decision must, before prescribing a voluntary assisted dying substance for the person, inform the person, in writing, of the following—

(a)

the S4 substance or S8 substance, or combination of substances, constituting the substance;

(b)

that the person is not under any obligation to self-administer the substance;

(c)

that the substance must be stored in accordance with requirements prescribed by regulation;

(d)

how to prepare and self-administer the substance;

(e)

the expected effects of self-administration of the substance;

(f)

the period within which the person is likely to die after self-administration of the substance;

(g)

the potential risks of self-administration of the substance;

(h)

that, if the person decides not to self-administer the substance, their contact person must give the substance to an authorised disposer for disposal;

(i)

that, if the person dies, their contact person must give any unused or remaining substance to an authorised disposer for disposal;

(j)

the name of the authorised supplier who will be supplying the voluntary assisted dying substance;

(k)

the name of 1 or more registered health practitioners or class of registered health practitioners who are authorised disposers.

(2)

The coordinating practitioner for a person who has made a practitioner administration decision must, before prescribing a voluntary assisted dying substance for the person, inform the person, in writing, of the following—

(a)

the S4 substance or S8 substance, or combination of substances, constituting the substance;

(b)

that the person is not under any obligation to have the substance administered to the person;

(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 person 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 person’s contact person must give any substance received by the person, the contact person or an agent of the contact person to an authorised disposer for disposal;

(h)

if the practitioner administration decision is made after the revocation of a self-administration decision—the name of 1 or more registered health practitioners or class of registered health practitioners who are authorised disposers.

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