Therapeutic Goods (Serious Scarcity and Substitutable Medicine) (Tocilizumab) Instrument 2021
made under section 30EK of the
Therapeutic Goods Act 1989
Compilation No. 1
Compilation date: 21 December 2021
Includes amendments up to: F2021L01852
About this compilation
This compilation
This is a compilation of the Therapeutic Goods (Serious Scarcity and Substitutable Medicine) (Tocilizumab) Instrument 2021 that shows the text of the law as amended and in force on 21 December 2021 (the compilation date).
The notes at the end of this compilation (the endnotes) include information about amending laws and the amendment history of provisions of the compiled law.
Uncommenced amendments
The effect of uncommenced amendments is not shown in the text of the compiled law. Any uncommenced amendments affecting the law are accessible on the Legislation Register (www.legislation.gov.au). The details of amendments made up to, but not commenced at, the compilation date are underlined in the endnotes. For more information on any uncommenced amendments, see the series page on the Legislation Register for the compiled law.
Application, saving and transitional provisions for provisions and amendments
If the operation of a provision or amendment of the compiled law is affected by an application, saving or transitional provision that is not included in this compilation, details are included in the endnotes.
Modifications
If the compiled law is modified by another law, the compiled law operates as modified but the modification does not amend the text of the law. Accordingly, this compilation does not show the text of the compiled law as modified. For more information on any modifications, see the series page on the Legislation Register for the compiled law.
Self‑repealing provisions
If a provision of the compiled law has been repealed in accordance with a provision of the law, details are included in the endnotes.
Contents
1 Name
3 Authority
4 Definitions
5 Declaration of serious scarcity
6 Substitution of scarce medicine by pharmacists
7 Period instrument in force
Schedule 1—Scarce medicine, substitutable medicine, dose unit equivalence and specific permitted circumstances
Part 1—Scarce medicine: tocilizumab pre‑filled syringe
Part 2—Scarce medicine: tocilizumab pre‑filled pen
Schedule 2—General permitted circumstances
Endnotes
Endnote 1—About the endnotes
Endnote 2—Abbreviation key
Endnote 3—Legislation history
Endnote 4—Amendment history
1 Name
This instrument is the Therapeutic Goods (Serious Scarcity and Substitutable Medicine) (Tocilizumab) Instrument 2021.
3 Authority
This instrument is made under section 30EK of the Therapeutic Goods Act 1989.
4 Definitions
Note: A number of expressions used in this instrument are defined in subsection 3(1) of the Act, including the following:
(a) medicine;
(b) Register;
(c) registration number.
In this instrument:
Act means the Therapeutic Goods Act 1989.
pharmacist has the same meaning as in subsection 30EK(6) of the Act.
prescriber means the person who:
(a) is authorised under a law of a state or territory to prescribe medicine, and
(b) prescribed the scarce medicine for the patient.
scarce medicine has the meaning given by section 5.
substitutable medicine has the meaning given by section 6.
5 Declaration of serious scarcity
For paragraph 30EK(1)(a) of the Act, a serious scarcity of the medicine specified in column 2 of each item in the tables in Part 1 and Part 2 of Schedule 1 (the scarce medicine) across the whole of Australia is declared.
6 Substitution of scarce medicine by pharmacists
For paragraph 30EK(1)(b) of the Act, in relation to each item mentioned in the tables in Part 1 and Part 2 of Schedule 1, the medicine specified in column 3 (the substitutable medicine) is permitted to be dispensed by a pharmacist in substitution for the scarce medicine specified in column 2, in the circumstances specified in:
(a) column 5 of that item (the specific permitted circumstances); and
(b) the table in Schedule 2 (the general permitted circumstances).
Note: Substitution is only permitted where both the specific permitted circumstances and the general permitted circumstances exist.
7 Period instrument in force
This instrument remains in force until 30 April 2022.
Schedule 1—Scarce medicine, substitutable medicine, dose unit equivalence and specific permitted circumstances
Note: See sections 5 and 6.
Part 1—Scarce medicine: tocilizumab pre‑filled syringe
Scarce medicine, substitutable medicine, dose unit equivalence and specific permitted circumstances | ||||
Column 1 | Column 2 | Column 3 | Column 4 | Column 5 |
Item | Scarce medicine | Substitutable medicine | Dose unit equivalence | Specific permitted circumstances |
1 | ACTEMRA tocilizumab (rch) 162 mg/0.9 mL solution for injection pre‑filled syringe, registration number 234034 | ACTEMRA tocilizumab (rch) 162 mg/0.9 mL solution for injection pre‑filled pen, ACTPen Autoinjector, registration number 296808 | one pre‑filled pen of the substitutable medicine containing tocilizumab (rch) 162 mg/0.9 mL solution is equivalent to one pre‑filled syringe of the scarce medicine containing tocilizumab (rch) 162 mg/0.9 mL solution | all of the following: (a) the patient is at least 18 years of age; (b) the pharmacist has advised the patient or person acting on behalf of the patient: (i) to obtain instructions from the prescriber, or a general practitioner or rheumatology nurse, in relation to the administration of the substitutable medicine; and (ii) of the number of dose units of substitutable medicine that must be taken by the patient in substitution for the prescribed dose of scarce medicine, based on the dose unit equivalence specified in column 4 |
Part 2—Scarce medicine: tocilizumab pre‑filled pen
Scarce medicine, substitutable medicine, dose unit equivalence and specific permitted circumstances | |||||
Column 1 | Column 2 | Column 3 | Column 4 | Column 5 | |
Item | Scarce medicine | Substitutable medicine | Dose unit equivalence | Specific permitted circumstances | |
1 | ACTEMRA tocilizumab (rch) 162 mg/0.9 mL solution for injection pre‑filled pen, ACTPen Autoinjector, registration number 296808 | ACTEMRA tocilizumab (rch) 162 mg/0.9 mL solution for injection pre‑filled syringe, registration number 234034 | one pre-filled syringe of the substitutable medicine containing tocilizumab (rch) 162 mg/0.9 mL solution is equivalent to one pre‑filled pen of the scarce medicine containing tocilizumab (rch) 162 mg/0.9 mL solution | all of the following: (a) the patient is at least 18 years of age; (b) the pharmacist has advised the patient or person acting on behalf of the patient: (i) to obtain instructions from the prescriber, or a general practitioner or rheumatology nurse, in relation to the administration of the substitutable medicine; and (ii) of the number of dose units of substitutable medicine that must be taken by the patient in substitution for the prescribed dose of scarce medicine, based on the dose unit equivalence specified in column 4 | |
Schedule 2—General permitted circumstances
Note: See section 6.
General permitted circumstances | |
Column 1 | Column 2 |
Item | Circumstances |
1 | the patient, or person acting on behalf of the patient, has evidence of a valid prescription for the scarce medicine, unless otherwise permitted by law |
2 | the pharmacist does not have access to the scarce medicine |
3 | the prescriber has not indicated on the prescription for the scarce medicine that substitution is not permitted |
4 | the pharmacist has exercised professional judgement and determined that the patient is suitable to receive the substitutable medicine |
5 | the amount of substitutable medicine dispensed would result in the patient receiving sufficient medicine to ensure an equivalent dosage regimen and duration to that prescribed in relation to the scarce medicine |
6 | the patient, or person acting on behalf of the patient, has consented to receiving the substitutable medicine |
7 | the pharmacist makes a record of dispensing the substitutable medicine in substitution of the scarce medicine at the time of dispensing |
8 | the pharmacist has an established procedure to notify the prescriber of the substitution at the time of, or as soon as practical after, dispensing the substitutable medicine |
Endnotes
Endnote 1—About the endnotes
The endnotes provide information about this compilation and the compiled law.
The following endnotes are included in every compilation:
Endnote 1—About the endnotes
Endnote 2—Abbreviation key
Endnote 3—Legislation history
Endnote 4—Amendment history
Abbreviation key—Endnote 2
The abbreviation key sets out abbreviations that may be used in the endnotes.
Legislation history and amendment history—Endnotes 3 and 4
Amending laws are annotated in the legislation history and amendment history.
The legislation history in endnote 3 provides information about each law that has amended (or will amend) the compiled law. The information includes commencement details for amending laws and details of any application, saving or transitional provisions that are not included in this compilation.
The amendment history in endnote 4 provides information about amendments at the provision (generally section or equivalent) level. It also includes information about any provision of the compiled law that has been repealed in accordance with a provision of the law.
Misdescribed amendments
A misdescribed amendment is an amendment that does not accurately describe the amendment to be made. If, despite the misdescription, the amendment can be given effect as intended, the amendment is incorporated into the compiled law and the abbreviation “(md)” added to the details of the amendment included in the amendment history.
If a misdescribed amendment cannot be given effect as intended, the abbreviation “(md not incorp)” is added to the details of the amendment included in the amendment history.
Endnote 2—Abbreviation key
ad = added or inserted | o = order(s) |
am = amended | Ord = Ordinance |
amdt = amendment | orig = original |
c = clause(s) | par = paragraph(s)/subparagraph(s) |
C[x] = Compilation No. x | /sub‑subparagraph(s) |
Ch = Chapter(s) | pres = present |
def = definition(s) | prev = previous |
Dict = Dictionary | (prev…) = previously |
disallowed = disallowed by Parliament | Pt = Part(s) |
Div = Division(s) | r = regulation(s)/rule(s) |
exp = expires/expired or ceases/ceased to have | reloc = relocated |
effect | renum = renumbered |
F = Federal Register of Legislation | rep = repealed |
gaz = gazette | rs = repealed and substituted |
LA = Legislation Act 2003 | s = section(s)/subsection(s) |
LIA = Legislative Instruments Act 2003 | Sch = Schedule(s) |
(md) = misdescribed amendment can be given | Sdiv = Subdivision(s) |
effect | SLI = Select Legislative Instrument |
(md not incorp) = misdescribed amendment | SR = Statutory Rules |
cannot be given effect | Sub‑Ch = Sub‑Chapter(s) |
mod = modified/modification | SubPt = Subpart(s) |
No. = Number(s) | underlining = whole or part not |
| commenced or to be commenced |
Endnote 3—Legislation history
Name | Registration | Commencement | Application, saving and transitional provisions |
Therapeutic Goods (Serious Scarcity and Substitutable Medicine) (Tocilizumab) Instrument 2021 | 06 Aug 2021 (F2021L01086) | 07 Aug 2021 | |
Therapeutic Goods (Serious Scarcity and Substitutable Medicine) (Tocilizumab) Amendment Instrument 2021 | 20 Dec 2021 (F2021L01852) | 21 Dec 2021 | |
Endnote 4—Amendment history
Provision affected | How affected |
s 2..................... | rep LA s 48D |
s 7..................... | am F2021L01852 |