Western Australian Consolidated Regulations

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POISONS REGULATIONS 1965 - REG 51F

51F .         Sch. 8 poisons not to be prescribed to be used for over 60 days unless authorised by CEO

        (1)         A medical practitioner shall not write, issue or authorise a prescription or document prescribing the use, sale or supply of a poison included in Schedule 8, or supply a poison included in Schedule 8, for the treatment of a person, other than a drug addict, for a period in excess of 60 days, or for periods that in the aggregate over the preceding 12 months exceed 60 days, or for a course of treatment exceeding 60 days, unless he has first obtained written authorisation to do so from the CEO.

        (2)         Where a medical practitioner has written, issued or authorised a prescription or document prescribing the use, sale or supply of a poison included in Schedule 8, for the treatment of a person other than a drug addict, or supplied a poison included in Schedule 8 for the treatment of a person, other than a drug addict, for a period of 60 days, or for periods that in the aggregate over the preceding 12 months exceed 60 days, or for a course of treatment exceeding 60 days, the medical practitioner shall not thereafter write, issue or authorise a prescription or document prescribing the use, sale or supply of a poison included in Schedule 8 in relation to that person or supply a poison included in Schedule 8 in relation to that person unless — 

            (a)         the medical practitioner has first obtained written authorisation under this regulation to do so from the CEO; or

            (b)         the CEO has issued an authorisation under this regulation to do so in relation to that person and the authorisation is current.

        (3)         Notwithstanding any authorisation referred to in subregulation (1) or (2) a medical practitioner shall not write, issue or authorise a prescription or document prescribing the use, sale or supply of methadone or buprenorphine for the treatment of a person or supply methadone or buprenorphine for the treatment of a person except for a person suffering from intractable pain arising from a condition of health other than addiction to drugs.

        (4)         In any authorisation issued for the purposes of subregulation (1) or (2) given with respect to a particular person the CEO may specify that any one or more of the conditions and restrictions set out below apply, namely — 

            (a)         that the prescription be issued by or the treatment be administered by a specified medical practitioner;

            (b)         that only a specified poison included in Schedule 8 be prescribed or used for treatment;

            (c)         that the type of the poison included in Schedule 8 specified be of the type specified;

            (d)         that the amount to be prescribed or used for treatment shall not exceed the amount specified;

            (e)         that the amount to be prescribed or used on any one day shall not exceed the amount specified;

            (f)         that the concentration to be prescribed shall not exceed the concentration specified;

            (g)         that the intervals between the issue of prescriptions or the administration of the poison included in Schedule 8 shall be such as are specified;

            (h)         that the prescription be supplied at the pharmacy specified;

                  (i)         that the amount dispensed on a single prescription not exceed such amount as is specified;

            (j)         that the amount that may be supplied on any one day shall not exceed such amount as is specified.

        (5)         An authorisation issued for the purposes of subregulation (1) or (2) is valid for such period as is specified unless revoked by the CEO before the expiration of that period.

        (6)         A medical practitioner shall not write, issue or authorise a prescription or document prescribing the use, sale or supply of a poison included in Schedule 8 or supply a poison included in Schedule 8 otherwise than in accordance with such conditions and restrictions as are specified.

        (7)         A pharmacist shall not sell or supply a poison included in Schedule 8 otherwise than in accordance with such conditions and restrictions as are specified pursuant to this regulation.

        (8)         An authorisation issued prior to 1 October 1980 is valid until revoked by the CEO or until it expires whichever first occurs.

        [Regulation 51F inserted in Gazette 3 Feb 1995 p. 342‑3; amended in Gazette 19 Mar 1996 p. 1230‑1; 11 Apr 1997 p. 1833; 16 Nov 2001 p. 5985; 15 Dec 2006 p. 5630 and 5631; 1 Oct 2010 p. 5079‑80.]

        [Heading inserted in Gazette 12 Aug 2003 p. 3664; amended in Gazette 15 Sep 2009 p. 3573.]



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