EXPLANATORY STATEMENT
National Health Act 1953
National Health (Price and Special Patient Contribution)
Amendment Determination 2011 (No. 5)
PB 50 of 2011
Purpose
This legislative instrument amends the National Health (Price and Special Patient Contribution) Determination 2010 ( PB 109 of 2010) which provides for price determinations in relation to brands of pharmaceutical items for which the Minister and the responsible person have not been able to make a price agreement. The Determination is made under section 85B of the National Health Act 1953 (the Act). The amendment amends Schedule 1 of PB 109 of 2010.
Background – the Pharmaceutical Benefits Scheme
Part VII of the Act is the legislative basis of the Pharmaceutical Benefits Scheme (PBS) under which the Commonwealth provides reliable, timely, and affordable access to a wide range of medicines for all Australians.
Subsection 85(1) provides that pharmaceutical benefits are to be provided by the Commonwealth in accordance with Part VII.
In the case of ready-prepared pharmaceutical benefits, the pharmaceutical benefit is a brand of a pharmaceutical item. That is, it is a brand of a listed drug, in a form and with a manner of administration, declared and determined under various provisions of Part VII.
Part VII also provides for numerous other matters, including pricing matters and matters relating to payments by the Commonwealth and charges to patients for pharmaceutical benefits. This Determination concerns such matters.
Background – the Determination
The Act provides for the Minister and the responsible person to agree a price that is taken to be the appropriate maximum price for sales of a brand of a pharmaceutical item to approved pharmacists (section 85AD). Section 85B of the Act applies if the Minister and the responsible person have been unable to reach an agreement.
Subsection 85B(2) provides that the Minister may determine an amount that is taken to be the appropriate maximum price for sales of a brand of a pharmaceutical item to approved pharmacists. This is termed the ‘Determined Price’.
Subsection 85B(3) provides that the Minister may determine an amount that is taken to be the price claimed by the responsible person as the appropriate maximum price for sales of the brand of the pharmaceutical item to approved pharmacists. This is termed the ‘Claimed Price’.
The Determined Price is the approved price to pharmacists and is used as the basis for working out the Commonwealth price for the brand of the pharmaceutical item (section 98B of the Act). 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 (ie, the price that would be the Commonwealth price if the responsible person’s claimed price had become the approved price to pharmacists) and the Commonwealth price for the brand is defined in subsection 85B(4) 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(5) 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(5) 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 Determination contains determinations of:
- Determined Prices (under subsection 85B(2) of the Act);
- Claimed Prices (under subsection 85B(3) of the Act); and
Changes effected by this Determination
A provision-by-provision description of this instrument is contained in Attachment 1.
This instrument amends PB 109 of 2010 by amending Schedule 1, Determined and Claimed Prices.
The effect of the Schedule 1 amendments is to remove one brand of the pharmaceutical item bromocriptine in the pack sizes of 30 and 60. It also shows the increase and decrease to existing pharmaceutical items, including a pharmaceutical item that has a therapeutic group premium and inserts a new pharmaceutical item sumatriptan.
The changes made in this instrument to matters determined under section 85B of the Act since the last amendment made on 1 July 2011, are set out in Attachment 2 to this Explanatory Statement and is titled Summary of Changes.
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. If the Minister and the responsible person cannot agree on a price, further consultation occurs with the responsible person, and thereafter the Minister determines the price that will be the approved price to pharmacists for the brand. The Minister also determines the corresponding price claimed by the responsible person which is used to calculate the special patient contribution that will apply to the brand.
The Determination
A provision by provision description of the Determination is contained in Attachment 1.
The Amendment Determination commences on 1 August 2011.
This instrument is a legislative instrument for the purposes of the Legislative Instruments Act 2003.
ATTACHMENT 1
PROVISION BY PROVISION DESCRIPTION OF THE AMENDMENT DETERMINATION
Section 1 Name of Determination
This section provides that this Determination is the National Health (Price and Special Patient Contribution) Amendment Determination 2011 (No. 5) and may also be cited as PB 50 of 2011.
Section 2 Commencement
This section provides that the Amendment Determination commences on 1 August 2011.
Section 3 Amendment of PB 109 of 2010
This section provides that Schedule 1 of the Instrument amends the determination under section 85B of the Act the National Health (Price and Special Patient Contribution) Determination 2010 (PB 109 of 2010).
Schedule 1 Amendments
Schedule 1 sets out the amendments to Determination PB 109 of 2010.
ATTACHMENT 2
SUMMARY OF CHANGES
SCHEDULE 1
Brands to which a brand premium no longer applies
Bromocriptine | Tablet 2.5 mg (as mesylate) [Quantity or Number of | Parlodel |
| Tablet 2.5 mg (as mesylate) [Quantity or Number of | Parlodel |
Brand with new brand premium
Sumatriptan | Tablet 50 mg (as succinate) | Imigran |
Brands with an increased brand premium
Amoxycillin with Clavulanic Acid | 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 | Augmentin Duo Forte |
| 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 |
Lamotrigine | Tablet 5 mg | Lamictal |
| Tablet 25 mg | Lamictal |
| Tablet 50 mg | Lamictal |
| Tablet 100 mg | Lamictal |
| Tablet 200 mg | Lamictal |
Ranitidine | Tablet 150 mg (as hydrochloride) | Zantac |
| Tablet 300 mg (as hydrochloride) | Zantac |
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 |
Brands with a price change and decreased brand premium
Escitalopram | Tablet 10 mg (as oxalate) | Lexapro |
| Tablet 20 mg (as oxalate) | Lexapro |
Meloxicam | Tablet 7.5 mg | Mobic |
| Tablet 15 mg | Mobic |
Methylprednisolone | Injection containing methylprednisolone acetate 40 mg in 1 mL | Depo-Medrol |
Nifedipine | Tablet 10 mg | Adalat 10 |
| Tablet 60 mg (controlled release) | Adalat Oros 60 |
Salbutamol | Pressurised inhalation 100 micrograms (as sulfate) per dose, 200 doses (CFC-free formulation) | Ventolin CFC-Free |
Valproic Acid | Tablet (enteric coated) containing sodium valproate | Epilim EC |
| Tablet (enteric coated) containing sodium valproate | Epilim EC |
Brands with a price change and an increased brand premium
Lercanidipine | Tablet containing lercanidipine hydrochloride 10 mg | Zanidip |
| Tablet containing lercanidipine hydrochloride 20 mg | Zanidip |
Brands with a price change but no change in brand premium
Felodipine | Tablet 2.5 mg (extended release) | Plendil ER |
| Tablet 5 mg (extended release) | Plendil ER |
| Tablet 10 mg (extended release) | Plendil ER |
Nifedipine | Tablet 20 mg | Adalat 20 |
| Tablet 30 mg (controlled release) | Adalat Oros 30 |
Brand with a price change but no change in therapeutic group premium
Nifedipine | Tablet 20 mg (controlled release) | Adalat Oros 20 |