National Health (Price and Special Patient Contribution) Amendment Determination 2015 (No. 3) (PB 40 of 2015)

Administered by Department of Health, Disability and Ageing

Legislation au F2015L00590 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

NATIONAL HEALTH ACT 1953

NATIONAL HEALTH (PRICE AND SPECIAL PATIENT CONTRIBUTION) AMENDMENT DETERMINATION 2015 (No. 3)

PB 40 of 2015

 

Authority

This legislative instrument, made under section 85B of the National Health Act 1953 (the Act) amends the National Health (Price and Special Patient Contribution) Determination 2010 (PB 109 of 2010) (the Principal Determination).

Subsections 85B(2), (3) and (4) of the National Health Act 1953 (the Act) provide for the Minister to determine, respectively, determined prices, claimed prices and the circumstances in which the Commonwealth will pay a special patient contribution.  The National Health (Price and Special Patient Contribution) Determination 2010 (the Principal Determination) contains determinations of these matters.

Variation and revocation

Unless there is an express power to revoke or vary PB 109 of 2010 cited in this Instrument and explanatory statement, subsection 33(3) of the Acts Interpretation Act 1901 is relied upon to revoke or vary PB 109 of 2010.

Purpose

The Act provides for the Minister and the responsible person to agree a price that is taken to be the appropriate maximum price of a brand of a pharmaceutical item for the purposes of Part VII of the Act (section 85AD).  Section 85B of the Act applies if the Minister and the responsible person have been unable to reach an agreement on a price for the pricing quantity.  Whether or not an agreement is made for the pricing quantity, section 85B also applies if the responsible person is dissatisfied with the proportional ex-manufacturer prices that will apply to other pack quantities.   

Subsection 85B(2) provides that the Minister may determine, by reference to the pricing quantity of a brand of a pharmaceutical item, an amount that is taken to be the appropriate maximum price of the brand for the purposes of Part VII of the Act.  This is termed the ‘Determined Price’ in this Determination.

Subsection 85B(3) provides that the Minister may determine, by reference to a pack quantity of a brand of the pharmaceutical item, an amount that is taken to be the price claimed by the responsible person for the pack quantity of the brand, for the purposes of Part VII of the Act.  This is termed the ‘Claimed Price’ in this Determination.

The Determined Price is the approved ex-manufacturer price and is used as the basis for working out the Commonwealth price for the brand of the pharmaceutical item (section 98B of the Act); for pack quantities other than the pricing quantity, the proportional ex-manufacturer price is used as the basis.  Approved pharmacists are entitled to payment from the Commonwealth equal to the Commonwealth price less the applicable patient co-payment (section 99 of the Act).

The difference between the responsible person’s Commonwealth price for a pack quantity (ie, the price that would be the Commonwealth price if the responsible person’s claimed price had become the approved ex-manufacturer price or the proportional ex-manufacturer price for that pack quantity) and the Commonwealth price for the pack quantity is defined in subsection 85B(5) of the Act as the special patient contribution.  An approved pharmacist may charge a patient an amount equal to the special patient contribution, in addition to any other amount that may be charged (subsection 87(2A) of the Act).

Subsection 85B(4) of the Act provides that the Minister may determine the circumstances in which the Commonwealth is to pay the special patient contribution for a brand.  In such cases, the Commonwealth payment to the pharmacist is increased by the amount of the special patient contribution (subsection 99(2AA) of the Act) and the pharmacist may not charge the patient this amount (subsection 87(2A) of the Act). 

The purpose of making subsection 85B(4) determinations is to enable patients for whom the base-priced brands (the ones without a special patient contribution) are not suitable, to obtain the higher priced brand (the one with the special patient contribution) without the need to pay the higher price.  In such cases the Commonwealth pays the special patient contribution.

This instrument (the Amending Determination) amends the Principal Determination by: removing one brand that is no longer PBS listed and reflecting for plain English reasons the price changes and decreases to multiple brand premiums which took legal effect on 1 April 2015 due to price disclosure reductions.

Consultation

This determination affects certain responsible persons with medicines listed on the PBS.  Before a pharmaceutical benefit is listed on the PBS, and from time to time thereafter, price negotiations occur between the responsible person and the Minister for the purpose of reaching a price agreement for section 85AD of the Act.  Consultation was considered unnecessary (or inappropriate) because this instrument essentially involves a price negotiation between the minister and the responsible persons.

A provision by provision description of the Amending Determination is contained in the Attachment.

This Determination commences on 1 May 2015.

This Determination is a legislative instrument for the purposes of the Legislative Instruments Act 2003.

 

 

 

 

 

ATTACHMENT

 

PROVISION BY PROVISION DESCRIPTION OF THE NATIONAL HEALTH (PRICE AND SPECIAL PATIENT CONTRIBUTION) AMENDMENT DETERMINATION 2015 (No. 3)

(PB 40 of 2015)

Section 1   Name of Determination

This section provides that the Determination is the National Health (Price and Special Patient Contribution) Amendment Determination 2015 (No. 3) and may also be cited as PB 40 of 2015.

Section 2   Commencement

This section provides that the Determination commences on 1 May 2015.

Section 3   Amendment of the National Health (Price and Special Patient Contribution) Determination 2010 (PB 109 of 2010).

This section provides that Schedule 1 amends the National Health (Price and Special Patient Contribution) Determination 2010 (PB 109 of 2010).

Schedule 1    Amendments commencing 1 May 2015

Schedule 1 sets out the amendments to the Principal Determination which commence on 1 May 2015.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


 

SUMMARY OF CHANGES

SCHEDULE 1

 

Brands with a price change and decreased brand premium

Amlodipine

Tablet 5 mg (as besylate)

Norvasc

Tablet 10 mg (as besylate)

Norvasc

Amoxycillin

Capsule 250 mg (as trihydrate)

Amoxil

Capsule 500 mg (as trihydrate)

Amoxil

Powder for oral suspension 125 mg (as trihydrate) per 5 mL, 100 mL

Amoxil

Powder for oral suspension 250 mg (as trihydrate) per 5 mL, 100 mL

Amoxil Forte

Tablet 1 g (as trihydrate)

Maxamox

Amoxycillin with Clavulanic Acid

Powder for oral suspension containing 125 mg amoxycillin (as trihydrate) with 31.25 mg clavulanic acid (as potassium clavulanate) per 5 mL, 75 mL

Augmentin

Powder for oral suspension containing 400 mg amoxycillin (as trihydrate) with 57 mg clavulanic acid (as potassium clavulanate) per 5 mL, 60 mL

Augmentin Duo 400

Tablet containing 500 mg amoxycillin (as trihydrate) with 125 mg clavulanic acid (as potassium clavulanate)

Augmentin Duo

Tablet containing 875 mg amoxycillin (as trihydrate) with 125 mg clavulanic acid (as potassium clavulanate)

Augmentin Duo forte

Atenolol

Tablet 50 mg

Tenormin

Bisoprolol

Tablet containing bisoprolol fumarate
2.5 mg

Bicor

Tablet containing bisoprolol fumarate
5 mg

Bicor

Tablet containing bisoprolol fumarate
10 mg

Bicor

Candesartan

Tablet containing candesartan cilexetil
4 mg

Atacand

Tablet containing candesartan cilexetil
8 mg

Atacand

Tablet containing candesartan cilexetil 16 mg

Atacand

Tablet containing candesartan cilexetil 32 mg

Atacand

Cyproterone

Tablet containing cyproterone acetate
50 mg (pricing quantity 20)

Androcur

Tablet containing cyproterone acetate
50 mg (pricing quantity 50)

Androcur

Tablet containing cyproterone acetate 100 mg

Androcur-100

Diclofenac

Tablet (enteric coated) containing diclofenac sodium 25 mg

Voltaren 25

Tablet (enteric coated) containing diclofenac sodium 50 mg

Voltaren 50

Doxycycline

Capsule 100 mg (as hydrochloride) (containing enteric coated pellets) (pricing quantity 7)

Doryx

Mayne Pharma Doxycycline

 

Capsule 100 mg (as hydrochloride) (containing enteric coated pellets) (pricing quantity 21)

Doryx

Mayne Pharma Doxycycline

 

Capsule 50 mg (as hydrochloride) (containing enteric coated pellets)

Doryx

Mayne Pharma Doxycycline

 

Enalapril

Tablet containing enalapril maleate
10 mg

Renitec

Tablet containing enalapril maleate
20 mg

Renitec 20

Escitalopram

Tablet 10 mg (as oxalate)

Lexapro

Tablet 20 mg (as oxalate)

Lexapro

Felodipine

Tablet 2.5 mg (extended release)

Plendil ER

Tablet 5 mg (extended release)

Plendil ER

Tablet 10 mg (extended release)

Plendil ER

Fluoxetine

Capsule 20 mg (as hydrochloride)

Prozac 20

Tablet, dispersible, 20 mg (as hydrochloride)

Prozac Tab

Fluvoxamine

Tablet containing fluvoxamine maleate 50 mg

Luvox

Tablet containing fluvoxamine maleate 100 mg

Luvox

Frusemide

Tablet 20 mg

Lasix-M

Tablet 40 mg

Lasix

Isosorbide Mononitrate

Tablet 60 mg (sustained release)

Imdur Durule

Monodur 60 mg

 

Tablet 120 mg (sustained release)

Imdur 120 mg

Lamotrigine

Tablet 5 mg

Lamictal

Tablet 25 mg

Lamictal

Tablet 50 mg

Lamictal

Tablet 100 mg

Lamictal

Tablet 200 mg

Lamictal

Lercanidipine

Tablet containing lercanidipine hydrochloride 10 mg

Zanidip

Tablet containing lercanidipine hydrochloride 20 mg

Zanidip

Lisinopril

Tablet 5 mg

Zestril

Tablet 10 mg

Prinivil 10

Zestril

 

Tablet 20 mg

Prinivil 20

Zestril

 

Meloxicam

Capsule 7.5 mg

Mobic

Capsule 15 mg

Mobic

Tablet 7.5 mg

Mobic

Tablet 15 mg

Mobic

Metformin

Tablet containing metformin hydrochloride 500 mg

Diabex

Tablet (extended release) containing metformin hydrochloride 500  mg

Diabex XR

Tablet containing metformin hydrochloride 850 mg

Diabex 850

Glucophage

 

Tablet containing metformin hydrochloride 1 g

Diabex 1000

Tablet (extended release) containing metformin hydrochloride 1 g

Diabex XR 1000

Methylprednisolone

Injection containing methylprednisolone acetate 40 mg in 1 mL

Depo-Medrol

Mirtazapine

Tablet 15 mg (orally disintegrating)

Avanza SolTab

Tablet 30 mg

Avanza

Tablet 30 mg (orally disintegrating)

Avanza SolTab

Tablet 45 mg

Avanza

Tablet 45 mg (orally disintegrating)

Avanza SolTab

Moclobemide

Tablet 150 mg

Aurorix

Tablet 300 mg

Aurorix 300 mg

Omeprazole

Tablet 20 mg (as magnesium)

Losec Tablets

Perindopril

Tablet containing perindopril arginine 2.5 mg

Coversyl 2.5mg

PREXUM 2.5

 

Pravastatin

Tablet containing pravastatin sodium
10 mg

Pravachol

Tablet containing pravastatin sodium
20 mg

Pravachol

Tablet containing pravastatin sodium
40 mg

Pravachol

Tablet containing pravastatin sodium
80 mg

Pravachol

Prochlorperazine

Tablet containing prochlorperazine maleate 5 mg

Stemetil

Quinapril

Tablet 5 mg (as hydrochloride)

Accupril

Tablet 10 mg (as hydrochloride)

Accupril

Tablet 20 mg (as hydrochloride)

Accupril

Ranitidine

Tablet 150 mg (as hydrochloride)

Zantac

Tablet 300 mg (as hydrochloride)

Zantac

Sertraline

Tablet 50 mg (as hydrochloride)

Zoloft

Tablet 100 mg (as hydrochloride)

Zoloft

Sotalol

Tablet containing sotalol hydrochloride 80 mg

Sotacor

Tablet containing sotalol hydrochloride 160 mg

Sotacor

Sumatriptan

Tablet 50 mg (as succinate)

Imigran

Tablet (fast disintegrating) 50 mg (as succinate)

Imigran FDT

Tamoxifen

Tablet 20 mg (as citrate)

Nolvadex-D

Tramadol

Capsule containing tramadol hydrochloride 50 mg

Tramal

Tablet (sustained release) containing tramadol hydrochloride 100 mg

Tramal SR 100

Tablet (sustained release) containing tramadol hydrochloride 150 mg

Tramal SR 150

Tablet (sustained release) containing tramadol hydrochloride 200 mg

Tramal SR 200

Trandolapril

Capsule 500 micrograms

Gopten

Capsule 1 mg

Gopten

Capsule 2 mg

Gopten

Capsule 4 mg

Gopten

Valproic Acid

Tablet (enteric coated) containing sodium valproate 200 mg

Epilim EC

Tablet (enteric coated) containing sodium valproate 500 mg

Epilim EC

 

Deletion of Brand

Mianserin

Tablet containing mianserin hydrochloride 10 mg

Tolvon

 


Statement of Compatibility with Human Rights

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

National Health (Price and Special Patient Contribution) Amendment Determination 2015 (No. 3)

(PB 40 of 2015)

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, made under section 85B of the National Health Act 1953 (the Act), amends the National Health (Price and Special Patient Contribution) Determination 2010 (the Principal Determination), which provides for price determinations in relation to brands of pharmaceutical items listed on the Pharmaceutical Benefits Scheme (PBS) for which the Minister and the responsible person have not been able to make a price agreement.  It also provides for the circumstances in which the Commonwealth will pay the special patient contribution resulting from these price determinations. This instrument (the Amending Determination) amends the Principal Determination by: removing one brand that is no longer PBS listed and reflecting for plain English reasons the price changes and decreases to multiple brand premiums which took legal effect on 1 April 2015 due to price disclosure reductions.

Human rights implications

This legislative instrument engages Articles 2 and 12 of the International Covenant on Economic, Social and Cultural Rights (ICESCR) 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 is a benefit scheme which assists with advancement of this human right by providing for subsidised access by patients to medicines. The recommendatory role of the Pharmaceutical Benefits Advisory Committee (PBAC) ensures that decisions about subsidised access to medicines on the PBS are evidence-based.

Conclusion

This Legislative Instrument is compatible with human rights because it advances the protection of human rights.

 

 

 

Felicity McNeill

First Assistant Secretary
Pharmaceutical Benefits Division
Department of Health  

Overview

The National Health (Price and Special Patient Contribution) Amendment Determination 2015 (No. 3) amends the National Health (Price and Special Patient Contribution) Determination 2010, both made under the National Health Act 1953. This determination addresses the issue of setting prices for pharmaceutical brands listed on the Pharmaceutical Benefits Scheme (PBS) when price agreements cannot be reached between the Minister for Health and the responsible persons. It also outlines the circumstances under which the Commonwealth will contribute to the cost of certain higher-priced brands for patients who require them. This amendment was made to reflect price changes and decreases to brand premiums effective from 1 April 2015, and to remove a brand no longer listed on the PBS. The purpose of these amendments is to ensure that the pricing structure for PBS-listed pharmaceutical items remains current and appropriate, facilitating access to necessary medications while maintaining the financial sustainability of the scheme.

Scope and Application

The National Health (Price and Special Patient Contribution) Amendment Determination 2015 (No. 3) amends the National Health (Price and Special Patient Contribution) Determination 2010, which is made under section 85B of the National Health Act 1953. This legislation applies to brands of pharmaceutical items listed on the Pharmaceutical Benefits Scheme (PBS) for which the Minister and the responsible person have not been able to reach an agreement on the price for the pricing quantity or where the responsible person is dissatisfied with the proportional ex-manufacturer prices that will apply to other pack quantities. The Act also applies to the circumstances under which the Commonwealth will pay a special patient contribution. This Determination is applicable nationally across Australia, affecting responsible persons with medicines listed on the PBS. The Amending Determination removes one brand that is no longer PBS listed and updates the prices and brand premiums to reflect changes that took effect on 1 April 2015. The changes were made to accommodate price disclosure reductions. The application of this Act may be extended or restricted through subordinate instruments, which may include further amendments to the Principal Determination.

Key Provisions

The National Health (Price and Special Patient Contribution) Amendment Determination 2015 (No. 3) (F2015L00590) amends the National Health (Price and Special Patient Contribution) Determination 2010 (F2010L01090). This amendment affects pharmaceutical brands listed on the Pharmaceutical Benefits Scheme (PBS) where the Minister and the responsible person have not reached a price agreement. The main changes include the removal of a brand no longer listed on the PBS and the adjustment of prices and brand premiums effective from 1 April 2015 due to price disclosure reductions. The amendment also ensures that the language used is plain English for better understanding. The Act imposes several obligations on the parties involved. Firstly, it requires the Minister to determine the appropriate maximum price of a brand of a pharmaceutical item if an agreement cannot be reached with the responsible person. This is referred to as the 'Determined Price'. Secondly, the Minister may also determine the 'Claimed Price' for specific pack quantities of a pharmaceutical brand. Thirdly, the Act allows the Minister to determine when the Commonwealth will pay the special patient contribution for certain brands. This ensures that patients who need specific brands not covered under the base-priced options can still access them without having to bear the full cost themselves. The amendment does not explicitly state penalties for non-compliance with the provisions of the Determination. However, failure to adhere to the price determinations and the terms set out in the National Health Act 1953 could potentially lead to legal consequences. These may include civil or administrative penalties for non-compliance with health legislation, although specific penalties are not detailed within this Determination. Pharmacists who do not comply with the provisions regarding the special patient contribution may face scrutiny and potential penalties under the Act, including fines or other regulatory actions. This Determination is a legislative instrument under the Legislative Instruments Act 2003 and is made under section 85B of the National Health Act 1953. It is compatible with human rights as it assists in the progressive realisation of the right to the highest attainable standard of physical and mental health by providing for subsidised access to medicines through the PBS. The Pharmaceutical Benefits Advisory Committee ensures that decisions about access to medicines on the PBS are evidence-based, thereby protecting human rights.

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