National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4)

Administered by Department of Health, Disability and Ageing

Legislation au F2024L00609 Not in force Legislative Instrument

Legislation content

EXPLANATORY STATEMENT

 

National Health Act 1953

 

National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4)

 

PB 58 of 2024

 

Authority

 

This instrument, made under subsection 85AB(1) of the National Health Act 1953 (the Act), amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021)  (the Principal Determination).

 

The Principal Determination provides for the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS).

 

Purpose

 

This instrument makes amendments to the Principal Determination.

 

The Act provides that PBS listed drugs may be assigned to formularies identified as F1 and F2. F1 is intended for single branded drugs and F2 for drugs that have multiple brands, or are in a therapeutic group with other drugs with multiple brands. Drugs on F2 are subject to the provisions of the Act relating to price disclosure and guarantee of supply.

 

Section 84AC of the Act provides that a drug is on F1 or F2 if there is a determination in force under section 85AB that the drug is on F1 or F2.

 

Subsection 85AB(1) of the Act empowers the Minister (or delegate) to determine by legislative instrument that a listed drug is on F1 or F2. For a drug to be on F1, it must satisfy the criteria in subsection 85AB(4). This requires that there are no listed brands of pharmaceutical items that have the drug that are bioequivalent or biosimilar, and no listed brands of pharmaceutical items that have another drug in the same therapeutic group as the first drug that are bioequivalent or biosimilar. It also requires that the drug was not on F2 the day before the determination comes into effect. A drug may only be determined to be on F2 if it does not satisfy one or more of the criteria for F1 (subsection 85AB(3)).

 

When subsection 85AB(5) of the Act applies, which relates to listed drugs with a single brand combination item on the PBS, the listed drug is not placed on F1 or F2, but on the administrative combination drug list (CDL).

 

This instrument amends the Principal Determination by moving one currently listed F1 drug, testosterone to F2. In addition, it also removes one drug, pancrelipase from F1 and one drug, paraffin with retinol palmitate from F2 as these drugs will no longer be PBS listed from
1 June 2024.

 

 

 

 

Variation and revocation

 

Unless there is an express power to revoke or vary PB 33 of 2021 cited in this instrument, subsection 33(3) of the Acts Interpretation Act 1901 is relied upon to revoke or vary PB 33 of 2021.

 

Consultation

 

This instrument affects pharmaceutical companies with new medicines listing on the PBS.

Pancrelipase and paraffin with retinol palmitate are being removed from the PBS at the request of the pharmaceutical companies that sponsor the PBS listings.  Testosterone no longer meets the criteria for F1 set out in section 85AB(4) of the Act so is required to be moved to F2 under subsection 85AB(3). 

 

Before a drug is PBS listed and allocated to a formulary, there are detailed consultations about the drug with the responsible person and recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC). Any PBAC recommendation is made following receipt of a submission made by the affected pharmaceutical company. Two-thirds of the PBAC membership is from the following interests or professions: consumers, health economists, practising community pharmacists, general practitioners, clinical pharmacologists and medical specialists.

 

No additional consultation with experts was undertaken regarding this determination because consultation with the affected responsible persons and the PBAC drew on the knowledge of persons with relevant expertise.

 

Commencement

 

This instrument commences on 1 June 2024.

 

This instrument is a legislative instrument for the purposes of the Legislation Act 2003.

 

 

 

 

 

 

 

 

Statement of Compatibility with Human Rights

Prepared in accordance with Part 3 of the Human Rights (Parliamentary Scrutiny) Act 2011

National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4)
(PB 58 of 2024)

This legislative instrument is compatible with the human rights and freedoms recognised or declared in the international instruments listed in section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011.

Overview of the Legislative Instrument

This legislative instrument is made pursuant to subsection 85AB(1) of the National Health Act 1953 (the Act), which relates to listed drugs on F1 or F2. This instrument amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021) (the Principal Determination) which provides for the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS).

 

This instrument amends the Principal Determination by moving one currently listed F1 drug, testosterone to F2. In addition, it also removes one drug, pancrelipase from F1 and one drug, paraffin with retinol palmitate from F2 as these drugs will no longer be PBS listed from
1 June 2024.

 

Human rights implications

 

This legislative instrument engages Articles 2 and 12 of the International Covenant on Economic, Social and Cultural Rights by assisting with the progressive realisation by all appropriate means of the right of everyone to the enjoyment of the highest attainable standard of physical and mental health.

 

The PBS assists with the advancement of this human right by providing for subsidised access of medicines to patients. The recommendatory role of the PBAC ensures that decisions about subsidised access to medicines on the PBS are evidence-based.

 

The right to social security is contained in Article 9 of the International Covenant on Economic Social and Cultural Rights (ICESCR). It requires that a country must, within its maximum available resources, ensure access to a social security scheme that provides a minimum essential level of benefits to all individuals and families that will enable them to acquire at least essential health care. Countries are obliged to demonstrate that every effort has been made to use all resources that are at their disposal in an effort to satisfy, as a matter of priority, this minimum obligation.

 

It is noted that this amending instrument provides for changes reflecting the delisting of two drugs – pancrelipase and paraffin with retinol palmitate which will result in these drugs no longer being available at a subsidised price.

 

The delisting from the PBS of the drugs pancrelipase and paraffin with retinol palmitate, occurred at the request of the sponsors, Technipro PulmoMed Pty Ltd and AFT Pharmaceuticals (AU) Pty Ltd.  The PBAC advised that the delisting of these drugs will not result in unmet clinical need.

Patients accessing PBS subsidised medicines are usually required to pay a co-payment towards their cost. From 1 January 2024, these fees are up to $31.60 for general patients and up to $7.70 for concession card holders. These co-payments are payable for accessing all PBS subsidised medicines. The deletion of pancrelipase and paraffin with retinol palmitate is therefore unlikely to result in a negative financial impact for patients as alternatives are subsidised and the same maximum co-payments apply to all PBS listed medicines.

The UN Committee on Economic Social and Cultural Rights reports that there is a strong presumption that retrogressive measures taken in relation to the right to social security are prohibited under ICESCR. In this context, a retrogressive measure would be one taken without adequate justification that had the effect of reducing existing levels of social security benefits, or of denying benefits to persons or groups previously entitled to them. However, it is legitimate for a government to re-direct its limited resources in ways that it considers to be more effective at meeting the general health needs of all society, particularly the needs of the more disadvantaged members of society.

 

Conclusion

 

This legislative instrument is compatible with human rights. Human rights continue to be protected by retaining clinically important medicines on the PBS and placing them in formularies that ensure the most cost-effective pricing for supply of each medicine to Australians.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 Nikolai Tsyganov

 Assistant Secretary

Pricing and PBS Policy Branch

Technology Assessment and Access Division

Department of Health and Aged Care

Overview

The National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4) was enacted to amend the National Health (Listed Drugs on F1 or F2) Determination 2021, which governs the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS). This amendment was made under the authority of the National Health Act 1953 and aims to ensure that drugs are appropriately categorised within the PBS formularies to maintain efficient and cost-effective pharmaceutical benefits for Australians. The National Health Act 1953 empowers the Minister to determine by legislative instrument which listed drugs are placed on F1 or F2, thereby influencing the pricing and availability of these medications. This amendment specifically adjusts the formulary placements of certain drugs, reflecting changes in their market status or therapeutic groupings. The Australian Government, through the Department of Health and Aged Care, introduced this amendment to address the need for periodic updates to the PBS formularies in response to changes in pharmaceutical listings and market conditions. The amendment moves testosterone from F1 to F2, reflecting its current market status, and removes pancrelipase from F1 and paraffin with retinol palmitate from F2 due to their upcoming delisting from the PBS. This adjustment ensures that the PBS continues to provide access to essential medicines while maintaining cost-effective pricing structures.

Scope and Application

The National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4) amends the National Health (Listed Drugs on F1 or F2) Determination 2021, which governs the allocation of drugs to the F1 and F2 formularies within the Pharmaceutical Benefits Scheme (PBS). The Act applies to pharmaceutical companies and healthcare providers involved in the PBS, ensuring that the drugs allocated to the F1 and F2 formularies meet specific criteria for bioequivalence and therapeutic grouping. This amendment affects the listing status of certain drugs, including moving testosterone from F1 to F2, and removing pancrelipase from F1 and paraffin with retinol palmitate from F2 as these drugs will cease to be PBS listed from 1 June 2024. The instrument also incorporates provisions from the Acts Interpretation Act 1901 to facilitate the revocation or variation of the Principal Determination. The changes are designed to align with the ongoing evaluation and recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC), which ensures decisions are evidence-based and reflective of the current therapeutic needs of the Australian population.

Key Provisions

The National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4) (PB 58 of 2024) amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021) by altering the allocation of drugs within the Pharmaceutical Benefits Scheme (PBS). This amendment relocates testosterone from the F1 to the F2 formulary, while also removing pancrelipase from the F1 formulary and paraffin with retinol palmitate from the F2 formulary. These changes take effect from 1 June 2024. The F1 formulary is designated for single-branded drugs, while the F2 formulary is for drugs with multiple brands or those in therapeutic groups with multiple brands. The amendment is made under subsection 85AB(1) of the National Health Act 1953, which allows the Minister or a delegate to determine by legislative instrument the placement of listed drugs on either F1 or F2. The obligations imposed by this Act on the parties and entities it governs include the requirement for detailed consultation with pharmaceutical companies and recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC) before a drug is listed on the PBS. The PBAC comprises members from various healthcare professions and consumer representatives, ensuring that decisions about drug subsidies are evidence-based and consider a broad spectrum of interests. Additionally, the Act mandates that the criteria for placement on F1 or F2 are strictly adhered to, ensuring that only eligible drugs are placed in the appropriate formulary. Pharmaceutical companies must also provide information and justification for the listing or delisting of their drugs on the PBS. Failure to comply with the provisions of the Act may result in civil or criminal penalties. While the specific penalties are not detailed in the explanatory statement, the Act provides a framework under which breaches could lead to enforcement actions. For instance, incorrect placement of a drug in the wrong formulary or failure to consult with the PBAC could result in regulatory sanctions, including fines or other penalties as prescribed by law. The Act also allows for the revocation or variation of previous determinations, ensuring that the PBS remains current and reflects the most appropriate therapeutic and economic decisions. In summary, the National Health (Listed Drugs on F1 or F2) Amendment Determination 2024 (No. 4) makes specific amendments to the allocation of drugs within the PBS, requiring strict adherence to the criteria set forth in the Act. Pharmaceutical companies and the PBAC are key stakeholders in this process, and failure to comply with the Act's provisions could result in penalties. The Act ensures that the PBS remains a robust and efficient system for providing subsidised access to essential medicines.

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Sourced from the Federal Register of Legislation at 26 August 2026. For the latest information on Australian Government law please go to https://www.legislation.gov.au.