{"id":"F2005L02120","name":"National Health Act 1953 - Arrangements made under subparagraph 100(1)(b)(i) - Chemotherapy Pharmaceuticals Access Program (No. PB 22 of 2005)","slug":"f2005l02120","collection":"legislative_instrument","jurisdiction":"commonwealth","status":"repealed","isInForce":false,"actNumber":null,"makingDate":null,"administeringDepartment":null,"currentVersion":{"id":331615,"registerId":"commonwealth-F2005L02120-current","compilationNumber":null,"startDate":"2026-04-08","status":"Repealed","reasons":null,"registeredAt":null},"sections":[{"sectionNumber":"1","sectionType":"section","heading":"National Health Act 1953 - Arrangements made under subparagraph 100(1)(b)(i) - Chemotherapy Pharmaceuticals Access Program (No. PB 22 of 2005)","content":"---\nmeta-content-style-type: text/css\nmeta-content-type: application/xhtml+xml; charset=utf-8\nmeta-generator: Aspose.Words for .NET 20.2\ntitle: ABACAVIR SULFATE\n---\n\n?xml version=\"1.0\" encoding=\"utf-8\" standalone=\"no\"?>\n\nCOMMONWEALTH OF AUSTRALIA\n\nNational Health Act 1953\n\nARRANGEMENTS MADE UNDER SUBPARAGRAPH 100(1)(b)(i)\n\nCHEMOTHERAPY PHARMACEUTICALS ACCESS PROGRAM\n\nNo. PB 22 of 2005\n\n \n\n \n\nI, JOAN CORBETT, Assistant Secretary, Pharmaceutical Benefits Branch, Department of Health and Ageing and delegate of the Minister for Health and Ageing, pursuant to subparagraph 100(1)(b)(i) of the National Health Act 1953, hereby make the following Arrangements for the purpose of providing that an adequate supply of special pharmaceutical products will be available to persons who are receiving treatment with chemotherapy pharmaceuticals at public hospitals as non-admitted patients, day admitted patients or patients on discharge:\n\n \n\nCommencement\n\n \n\n1. (a) These Arrangements commence on 1 August 2005.\n\n \n\n(b) The Arrangements made on 26 May 2005 with effect from 1 June 2005 (No. PB 13 of 2005) are repealed with effect from the commencement of these Arrangements.\n\n \n\nDefinitions\n\n \n\n2. In these Arrangements:\n\n \n\n(a) unless the contrary intention appears, a word or phrase will be taken to have the same meaning as in the Act, the Regulations or a declaration, determination or other instrument made under Part VII of the Act or under the Regulations;\n\n \n\n(b) “Act” means the National Health Act 1953;\n\n \n\n(c) “Commission” means the Health Insurance Commission established by the Health Insurance Commission Act 1973;\n\n \n\n(d)          “chemotherapy pharmaceutical” means a special pharmaceutical product in relation to which, by virtue of paragraphs 5, 8 and 12, these Arrangements apply;\n\n(e) “HIC authority notification computer system” means a computer system operated by the Commission for the purpose of receiving messages from medical practitioners and sending authorisations for supply of chemotherapy pharmaceuticals or refusals of such authorisations, having an electronic mail address approved by the Managing Director;\n\n \n\n(f) “hospital” means a public hospital that is participating in the arrangements provided for in Appendix F to Australian Health Care Agreements;\n\n \n\n(g) “Managing Director” means the Managing Director of the Commission;\n\n \n\n(h) “medical practitioner” means a medical practitioner, within the meaning of the Health Insurance Act 1973, who is affiliated with the hospital in or at which the patient is receiving treatment;\n\n \n\n(i) “patient” means a person receiving treatment as a non-admitted patient, a day admitted patient or a patient on discharge of the hospital of which the approved hospital authority is the governing body;\n\n \n\n(j) “Regulations” means the National Health (Pharmaceutical Benefits) Regulations 1960 made under the Act.\n\n \n\n3. Except where otherwise specified in these Arrangements, the provisions of the Act and the Regulations, and declarations, determinations and other instruments made under the Act shall apply to the prescribing and supply of chemotherapy pharmaceuticals.\n\n \n\nEntitlement to receive chemotherapy pharmaceuticals under these Arrangements\n\n \n\n4. Subject to these Arrangements, a person who:\n\n \n\n(a)          is, or is to be treated as, an eligible person within the meaning of the Health Insurance Act 1973; and\n\n \n\n(b)          is receiving treatment as a non-admitted patient, a day admitted patient or a patient on discharge, of a hospital as defined in paragraph 2(f); and\n\n \n\n(c)          is receiving medical treatment by a medical practitioner, within the meaning of the Health Insurance Act 1973, who is affiliated with the hospital in or at which the patient is receiving treatment;\n\n \n\n is entitled to receive chemotherapy pharmaceuticals under these Arrangements without the payment or furnishing of money or other consideration other than a charge made in accordance with paragraphs 20 and 20A.\n\n \n\n5. The special pharmaceutical products to which these Arrangements apply are the chemotherapy pharmaceuticals specified in column 1 of Schedule 1.\n\n \n\n6. The prescribing of a chemotherapy pharmaceutical is authorised under these Arrangements only in the circumstances, if any, specified in column 2 of Schedule 1 in relation to the chemotherapy pharmaceutical.\n\n \n\n7. The following circumstances are specified in relation to each chemotherapy pharmaceutical:\n\n \n\n(a) where a class of persons is specified in column 2 of Schedule 1 — the chemotherapy pharmaceutical is to be supplied for the treatment of a person included in that class of persons; or\n\n \n\n\n(b) where a disease or condition is specified in column 2 of Schedule 1 —\n\n \n\n(i) if subsubparagraph (ii) does not apply — the chemotherapy pharmaceutical is to be supplied for the treatment of that disease or condition in relation to any person; or\n\n \n\n(ii) if the disease or condition is specified in relation to a specified class of persons — that the chemotherapy pharmaceutical is to be supplied for the treatment of that disease or condition in a person included in that class of persons; or\n\n \n\n(c) where a purpose is specified in column 2 of Schedule 1 — the chemotherapy pharmaceutical is to be supplied for that purpose.\n\n \n\n8. Where strength, type of unit, size of unit or other particulars of form are specified in column 2 of Schedule 2 or column 2 of Schedule 3 in relation to a special pharmaceutical product, each specified form of the product is a chemotherapy pharmaceutical, and these Arrangements do not apply in relation to the special pharmaceutical product in any other form.\n\n \n\n9. The manner of administration specified in column 3 of Schedule 2 or column 4 of Schedule 3 in relation to a chemotherapy pharmaceutical is the only manner of administration that may be directed to be used in relation to that product.\n\n \n\n10. The maximum quantity or number of units of a chemotherapy pharmaceutical that may, in one prescription, be directed to be supplied on any one occasion is:\n\n(a)           where the name of the chemotherapy pharmaceutical is specified in column 1 of Schedule 2 — the quantity or number, if any, specified in column 4 of that Schedule in relation to the chemotherapy pharmaceutical; or\n\n \n\n(b) where the name of the chemotherapy pharmaceutical is specified in column 1 of Schedule 3 and the chemotherapy pharmaceutical is prescribed in accordance with the provisions of column 3 of that Schedule — the quantity or number, if any, specified in column 5 of that Schedule in relation to the chemotherapy pharmaceutical.\n\n \n\n11. The maximum number of occasions, if any, on which the supply of a chemotherapy pharmaceutical may, in one prescription, be directed to be repeated is:\n\n(a) where the name of the chemotherapy pharmaceutical is specified in column 1 of Schedule 2 — the number, if any, specified in column 5 of that Schedule in relation to the chemotherapy pharmaceutical; or\n\n \n\n(b) where the name of the chemotherapy pharmaceutical is specified in column 1 of Schedule 3 and the chemotherapy pharmaceutical is prescribed in accordance with the provisions of column 3 of that Schedule — the number, if any, specified in column 6 of that Schedule in relation to the chemotherapy pharmaceutical.\n\n \n\n12. The name of the manufacturer or the names of the manufacturers denoted in accordance with the following table by letters specified in column 6 of Schedule 2 or column 7 of Schedule 3 in relation to a special pharmaceutical product is or are the brand or brands under which the special pharmaceutical product may be supplied as a chemotherapy pharmaceutical, and these Arrangements do not apply to the special pharmaceutical product as marketed under any other brand:\n\n \n\n- Letters Manufacturer’s Name Letters Manufacturer’s Name\n- AP AstraZeneca Pty Ltd MX Mayne Pharma Pty Ltd\n- AS Aspen Pharmacare Australia Pty Ltd NV Novartis Pharmaceuticals Australia Pty Ltd\n- AV Aventis Pharma Pty Limited OA Orphan Australia Pty Ltd\n- BQ Bristol-Myers Squibb Pharmaceuticals A Division of Bristol-Myers Squibb Australia Pty Ltd OR Organon (Australia) Pty Limited\n- PF Pfizer Pty Limited\n- PH Pharmacia Australia Pty Limited\n- BX Baxter Healthcare Pty Limited PU Pharmacia & Upjohn Pty Limited\n- FB Pierre Fabre Medicament Australia Pty Limited RO Roche Products Pty Ltd\n- SE Servier Laboratories (Aust.) Pty Ltd\n- GK GlaxoSmithKline Australia Pty Ltd SH Schering-Plough Pty Ltd\n- IT InterPharma Pty Ltd SI Sigma Pharmaceuticals Pty Ltd\n- JC Janssen-Cilag Pty Ltd SW Sanofi Synthelabo Australia Pty Limited\n- LY Eli Lilly Australia Pty Limited ZH Shinnick Pharmaceuticals Pty Limited\n- MK Merck Sharp & Dohme (Australia) Pty Ltd\n\n\n \n\nPrescribing of chemotherapy pharmaceuticals\n\n \n\n13. A medication chart prepared by a medical practitioner, on which is prescribed a chemotherapy pharmaceutical for the medical treatment of a patient of the hospital who is named on the medication chart, will be taken to be a duly written prescription within the meaning of regulation 19 of the Regulations, notwithstanding that it does not comply with the requirements of paragraphs 19(1)(a) and (b) of the Regulations, provided that:\n\n \n\n(a) the medication chart bears the number issued by the Commission, in pursuance of the function granted to it by paragraph 3C(a) of the Health Insurance Commission Regulations 1975 made under the Health Insurance Commission Act 1973, to the medical practitioner who prescribed the chemotherapy pharmaceutical; and\n\n \n\n(b) if the medication chart contains a direction, pursuant to paragraph 85A(2)(b) of the Act and subparagraph 19(1)(f)(ii) of the Regulations, that the supply of the chemotherapy pharmaceutical is to be repeated, that direction will be invalid; and\n\n \n\n(c) if the medication chart contains a direction for the supply of an increased quantity or number of units of the chemotherapy pharmaceutical pursuant to subsection 88(6) of the Act and regulation 24 of the Regulations, that direction will be taken to be a direction to supply the maximum quantity or number of units for that chemotherapy pharmaceutical as specified in Schedule 2 or Schedule 3, as the case may be; and\n\n\n(d) if the medication chart contains a direction for the supply of a quantity or number of units of a chemotherapy pharmaceutical greater than the maximum quantity for that chemotherapy pharmaceutical as specified in column 4 of Schedule 2, or column 5 of Schedule 3, as the case may be, an authorisation has been obtained, in accordance with paragraph 15, for the supply of that greater quantity or number of units; and\n\n \n\n(e) if the medication chart contains a direction for the supply of a chemotherapy pharmaceutical for which it is necessary to obtain the authorisation of the Managing Director pursuant to column 2 of Schedule 1, or column 3 of Schedule 3, an authorisation has been obtained, in accordance with paragraph 14, for the supply of the chemotherapy pharmaceutical.\n\n \n\n14. A medical practitioner who wishes to prescribe a chemotherapy pharmaceutical for which an authorisation has to be obtained pursuant to subparagraph 13(e) may:\n\n \n\n(a) seek that authorisation in accordance with the provisions of subparagraph 14(d) of the declaration in force under subsection 85(2) of the Act; or\n\n \n\n(b)          arrange for the authorisation to be sought, on behalf of the medical practitioner, by the approved hospital authority in accordance with paragraph 16.\n\n \n\n15. A medical practitioner who wishes to prescribe a quantity of a chemotherapy pharmaceutical for which an authorisation has to be obtained pursuant to subparagraph 13(d) may:\n\n \n\n(a) seek that authorisation in accordance with the provisions of regulation 13 of the Regulations; or\n\n \n\n(b) arrange for the authorisation to be sought, on behalf of the medical practitioner, by the approved hospital authority in accordance with paragraph 16.\n\n \n\n16. Where, pursuant to subparagraph 14(b) or 15(b), a medical practitioner arranges for an approved hospital authority to seek an authorisation for the supply of a chemotherapy pharmaceutical, a pharmacist employed by the approved hospital authority must, on behalf of the medical practitioner, submit details of the medication chart by giving to the HIC authority notification computer system, by computer message in a manner and form approved by the Managing Director, details of the medication chart that has been prepared and signed by the medical practitioner in accordance with regulation 19 of the Regulations, as modified by paragraph 13.\n\n \n\n17. Where, on behalf of a medical practitioner, a pharmacist employed by an approved hospital authority submits details of a medication chart to the HIC authority notification computer system in accordance with paragraph 16, and it is received by that computer system, the computer system may send a message, in a manner and form approved by the Managing Director, to the approved hospital authority, and:\n\n \n\n(a) if the message indicates that authorisation has been granted, the pharmacist employed by the approved hospital authority must complete the medication chart in accordance with the instructions contained in the message; or\n\n \n\n(b) if the message indicates that authorisation has not been granted, or the HIC authority notification computer system fails to send a message indicating whether or not authorisation has been granted, the medical practitioner may, if the medical practitioner so wishes, resubmit the details of the medication chart to the Managing Director in accordance with the provisions of subparagraph 14(d) of the declaration in force under subsection 85(2) of the Act or regulation 13 of the Regulations, as the case may be.\n\n \n\n18. When the HIC authority notification computer system has sent to the approved hospital authority a message indicating that authorisation has been granted, the supply of the chemotherapy pharmaceutical shall be taken to have been approved under these Arrangements.\n\n \n\nSupply of chemotherapy pharmaceuticals under these Arrangements\n\n \n\n19. The approved hospital authority will supply chemotherapy pharmaceuticals to the patients of the hospital as if medication charts were original prescriptions, provided that:\n\n \n\n(a) where a medication chart contains a direction to supply more than one chemotherapy pharmaceutical, the approved hospital authority must not, pursuant to regulation 26A of the Regulations, defer the supply of one or more of the chemotherapy pharmaceuticals; and\n\n \n\n(b) in lieu of the requirements of regulation 31 of the Regulations, a person authorised for the purpose by the approved hospital authority certifies on the medication chart that the chemotherapy pharmaceutical has been supplied and the date on which it was supplied, and signs his or her name.\n\n \n\nCost to patient of chemotherapy pharmaceuticals supplied under these Arrangements\n\n \n\n20. An approved hospital authority that supplies a chemotherapy pharmaceutical may charge the person to whom the chemotherapy pharmaceutical is supplied an amount equivalent to the amount that may be charged under subsection 87(2) of the Act for the supply of a pharmaceutical benefit to the person.\n\n \n\n20A. In addition to the amount that may be charged by an approved hospital authority under paragraph 20, an approved hospital authority which supplies a chemotherapy pharmaceutical which is:\n\n \n\n(i) named in column 1 of Schedule 4;\n\n \n\n(ii) in the form specified in column 2 of Schedule 4 in relation to that chemotherapy pharmaceutical;\n\n \n\n(iii) marketed under the brand specified in column 3 of Schedule 4 in relation to that chemotherapy pharmaceutical; and\n\n \n\n\n(iv) in the quantity or number of units specified in column 4 of Schedule 4 in relation to that chemotherapy pharmaceutical;\n\n \n\n may charge the person to whom the chemotherapy pharmaceutical is supplied the amount calculated by subtracting the amount specified in column 5 of Schedule 4 in relation to that chemotherapy pharmaceutical from the amount specified in column 6 of Schedule 4 in relation to that chemotherapy pharmaceutical.\n\n \n\n20B Notwithstanding anything else in these Arrangements, paragraph 20A of these Arrangements will not apply in respect of the chemotherapy pharmaceutical listed in the following table if the medication chart which directs the supply of the chemotherapy pharmaceutical was written before 1 August 2005 and supply is made before 1 March 2006:\n\n \n\n| Name of chemotherapy pharmaceutical | Form (strength, type, size, etc) | Brand |\n| --- | --- | --- |\n| Pemetrexed Disodium Heptahydrate | Powder for I.V. infusion equivalent to 500 mg pemetrexed, vial | LY |\n\n\n \n\nPayment to supplier of chemotherapy pharmaceuticals under these Arrangements\n\n \n\n21. An approved hospital authority that has supplied a chemotherapy pharmaceutical is entitled to be paid by the Commonwealth the amount, if any, by which the dispensed price for the supply of the chemotherapy pharmaceutical exceeds the amount that the approved hospital authority was entitled to charge under paragraph 20.\n\n \n\n22. The dispensed price for the supply of a chemotherapy pharmaceutical will be ascertained in accordance with the determination in force under subsection 99(4) of the Act in respect of the supply of pharmaceutical benefits by public hospitals.\n\n \n\n23. Regulation 22 and subregulations 25(2), (3) and (4) of the Regulations do not apply to the supply of chemotherapy pharmaceuticals under these Arrangements.\n\n \n\nClaims for payment for the supply of chemotherapy pharmaceuticals under these Arrangements\n\n \n\n24. The approved hospital authority must prepare an electronic pharmacy record in respect of each medication chart in respect of which a chemotherapy pharmaceutical has been supplied to a patient of the hospital, and must retain that electronic pharmacy record for not less than one year after the day on which the chemotherapy pharmaceutical was supplied.\n\n \n\n25. The electronic pharmacy record referred to in paragraph 24 must contain all information required to be included in a prescription record by Part 4 of the Schedule to the rules in force under subsection 99AAA(8) of the Act, as modified by paragraph 29 of these Arrangements.\n\n \n\n26. Subject to paragraph 27, a claim by the approved hospital authority in respect of chemotherapy pharmaceuticals supplied to the patients of the hospital may be furnished unaccompanied by the medication charts in respect of which chemotherapy pharmaceuticals have been supplied to the patients of the hospital.\n\n \n\n27. If the Managing Director notifies the approved hospital authority that a copy of all or any of the medication charts in respect of chemotherapy pharmaceuticals supplied to the patients of the hospital is required to be submitted, the approved hospital authority must submit a copy of each such medication chart to the Commission.\n\n \n\n28. If the Managing Director notifies the approved hospital authority that a copy of all or any of the electronic pharmacy records in respect of chemotherapy pharmaceuticals supplied to the patients of the hospital is required to be submitted, the approved hospital authority must submit a copy of each such electronic pharmacy record to the Commission.\n\n \n\n29. Information provided by electronic means to the Secretary by the approved hospital authority in respect of a claim in respect of chemotherapy pharmaceuticals supplied to the patients of the hospital will conform to the requirements of paragraph 5 of, and the Schedule to, the rules in force under subsection 99AAA(8) of the Act, provided that Part 4 of the Schedule to those rules is amended:\n\n \n\n(a) by omitting the specifications for the field “Prescriber Number” and substituting “Seven bytes numeric, right justified, zero filled, being the prescriber number of the prescribing medical practitioner, issued by the Commission in pursuance of the function granted to it by paragraph 3C(a) of the Health Insurance Commission Regulations made under the Health Insurance Commission Act 1973”; and\n\n \n\n(b) by omitting the field “Filler” and substituting the following field:\n\n“Field: Hospital patient indicator\n\nStart: 32\n\nEnd: 32\n\nSpecifications for field: One byte alphanumeric, value ‘H’ to indicate that the person for whose treatment the medication chart was written was a patient of the hospital; otherwise ‘0’\n\n \n\n \n\nDated this twenty-eighth day of July 2005.\n\n \n\n \n\n \n\n \n\n \n\n \n\nJOAN CORBETT\n\nAssistant Secretary\n\nPharmaceutical Benefits Branch\n\nDepartment of Health and Ageing\n\nDelegate of the Minister for Health and Ageing\n\n \n\n- Aprepitant In compliance with authority procedures set out in paragraph 14:\n- Management of nausea and vomiting associated with cytotoxic chemotherapy being used to treat malignancy, when aprepitant is used in combination with a 5-hydroxytryptamine type 3 receptor antagonist and dexamethasone, where treatment with aprepitant is limited to an initial dose of 125 mg and 2 subsequent doses of 80 mg per cycle of cytotoxic chemotherapy, and where the cytotoxic chemotherapy to be administered to the patient includes any of the following agents:altretamine;carmustine;cisplatin, when a single dose constitutes a cycle of chemotherapy;cyclophosphamide, at a dose of 1500 mg per square metre per day or greater;dacarbazine;procarbazine, when a single dose constitutes a cycle of chemotherapy;streptozocin\n- \"BCG Immunotherapeutic\" (Bacillus Calmette-Guérin/Connaught strain) Treatment of carcinoma in situ of the urinary bladder\n- \"BCG-Tice\" (Bacillus Calmette-Guérin/Tice strain) Primary and relapsing superficial urothelial carcinoma of the bladder\n- Bleomycin Sulfate Germ cell neoplasms\n- Lymphoma\n- Calcium Folinate In respect of the tablet equivalent to 15 mg folinic acid:\n- Antidote to folic acid antagonists\n- In respect of the injection equivalent to 50 mg folinic acid in 5 mL and injection equivalent to 100 mg folinic acid in 10 mL:\n- —\n- Carboplatin —\n- Cisplatin —\n- Cladribine In compliance with authority procedures set out in paragraph 14:\n- Hairy cell leukaemia\n- Cyclophosphamide —\n- Cytarabine —\n- Docetaxel In compliance with authority procedures set out in paragraph 14:\n- Advanced breast cancer after failure of prior therapy which includes an anthracycline\n- Advanced metastatic ovarian cancer after failure of prior therapy which includes a platinum compound\n- Locally advanced or metastatic non-small cell lung cancer\n- Dolasetron Mesylate Management of nausea and vomiting associated with cytotoxic chemotherapy being used to treat malignancy\n- Doxorubicin Hydrochloride —\n- Doxorubicin Hydrochloride - Pegylated Liposomal In compliance with authority procedures set out in paragraph 14:\n- Advanced epithelial ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen\n- Metastatic breast cancer, as monotherapy, after failure of prior therapy which includes capecitabine and a taxane\n- Metastatic breast cancer, as monotherapy, where therapy with capecitabine or a taxane is contraindicated\n- Epirubicin Hydrochloride —\n- Etoposide —\n- Etoposide Phosphate —\n- Fluorouracil Sodium —\n- Fotemustine In compliance with authority procedures set out in paragraph 14:\n- Metastatic malignant melanoma\n- Gemcitabine Hydrochloride In compliance with authority procedures set out in paragraph 14:\n- Advanced breast cancer in combination with paclitaxel after failure of prior therapy which includes an anthracycline\n- Advanced epithelial ovarian cancer, in combination with carboplatin, in patients who relapse more than 6 months after platinum-based therapy\n- Locally advanced or metastatic non-small cell lung cancer\n- Locally advanced or metastatic adenocarcinoma of the pancreas\n- Locally advanced or metastatic bladder cancer, when used in combination with cisplatin\n- Granisetron Hydrochloride Management of nausea and vomiting associated with cytotoxic chemotherapy being used to treat malignancy\n- Idarubicin Hydrochloride Acute myelogenous leukaemia\n- Ifosfamide Relapsed or refractory germ cell tumours following first-line chemotherapy\n- Relapsed or refractory sarcomas following first-line chemotherapy\n- Interferon Alfa-2a In respect of the injection 3,000,000 I.U. in 0.5 mL single dose pre-filled syringe:\n- In compliance with authority procedures set out in paragraph 14:\n- Hairy cell leukaemia\n- Myeloproliferative disease with excessive thrombocytosis\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- In respect of the injection 4,500,000 I.U. in 0.5 mL single dose pre-filled syringe, injection 6,000,000 I.U. in 0.5 mL single dose pre-filled syringe and injection 9,000,000 I.U. in 0.5 mL single dose pre-filled syringe:\n- In compliance with authority procedures set out in paragraph 14:\n- Myeloproliferative disease with excessive thrombocytosis\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Interferon Alfa-2b In respect of the solution for injection 18,000,000 I.U. in 1.2 mL multi-dose injection pen:\n- In compliance with authority procedures set out in paragraph 14:\n- Hairy cell leukaemia\n- Maintenance treatment of multiple myeloma once remission has been achieved with chemotherapy\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- In respect of the solution for injection 30,000,000 I.U. in 1.2 mL multi-dose injection pen:\n- In compliance with authority procedures set out in paragraph 14:\n- Maintenance treatment of multiple myeloma once remission has been achieved with chemotherapy\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Irinotecan Hydrochloride Trihydrate In compliance with authority procedures set out in paragraph 14:\n- Metastatic colorectal cancer in patients with a World Health Organisation performance status of 2 or less\n- Mesna Adjunctive therapy for use with ifosfamide or high dose cyclophosphamide\n- Methotrexate —\n- Mitozantrone Hydrochloride —\n- Ondansetron Management of nausea and vomiting associated with cytotoxic chemotherapy being used to treat malignancy\n- Ondansetron Hydrochloride Dihydrate Management of nausea and vomiting associated with cytotoxic chemotherapy being used to treat malignancy\n- Oxaliplatin In compliance with authority procedures set out in paragraph 14:\n- Metastatic colorectal cancer in patients with a World Health Organisation performance status of 2 or less, when used in combination with fluorouracil sodium and calcium folinate\n- Paclitaxel In compliance with authority procedures set out in paragraph 14:\n- Adjuvant treatment of node-positive, oestrogen receptor negative, breast cancer administered sequentially to doxorubicin hydrochloride and cyclophosphamide\n- Advanced breast cancer after failure of prior therapy which includes an anthracycline\n- Advanced metastatic ovarian cancer after failure of prior therapy which includes a platinum compound\n- Primary treatment of ovarian cancer in combination with a platinum compound\n- Locally advanced or metastatic non-small cell lung cancer\n- Pemetrexed Disodium Heptahydrate In compliance with authority procedures set out in paragraph 14:\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where treatment with paclitaxel or docetaxel is contraindicated\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where intolerance to treatment with either docetaxel or paclitaxel has developed\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where treatment with either docetaxel or paclitaxel has been unsuccessful\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where transfer to docetaxel or paclitaxel is likely to result in adverse clinical consequences\n- Raltitrexed In compliance with authority procedures set out in paragraph 14:\n- For use as a single agent in the treatment of advanced colorectal cancer\n- Rituximab In compliance with authority procedures set out in paragraph 14:\n- Relapsed or refractory low-grade B-cell non-Hodgkin's lymphoma\n- Relapsed or refractory follicular B-cell non-Hodgkin's lymphoma\n- Treatment of previously untreated, CD20 positive, diffuse large B-cell non-Hodgkin's lymphoma, in combination with chemotherapy\n- Temozolomide In respect of the capsule 5 mg, capsule 20 mg and capsule 100 mg:\n- In compliance with authority procedures set out in paragraph 14:\n- Glioblastoma multiforme concomitantly with radiotherapy\n- Recurrence of anaplastic astrocytoma following standard therapy\n- Recurrence of glioblastoma multiforme following standard therapy\n- Glioblastoma multiforme following radiotherapy\n- In respect of the capsule 250 mg:\n- In compliance with authority procedures set out in paragraph 14:\n- Recurrence of anaplastic astrocytoma following standard therapy\n- Recurrence of glioblastoma multiforme following standard therapy\n- Glioblastoma multiforme following radiotherapy\n- Thiotepa —\n- Topotecan Hydrochloride In compliance with authority procedures set out in paragraph 14:\n- Advanced metastatic ovarian cancer after failure of prior therapy which includes a platinum compound\n- Tropisetron Hydrochloride Management of nausea and vomiting associated with cytotoxic chemotherapy being used to treat malignancy\n- Vinblastine Sulfate —\n- Vincristine Sulfate —\n- Vinorelbine Tartrate In compliance with authority procedures set out in paragraph 14:\n- Advanced breast cancer after failure of prior therapy which includes an anthracycline\n- Locally advanced or metastatic non-small cell lung cancer\n\n\n \n\n \n\n| Aprepitant | Pack containing 1 capsule 125 mg and 2 capsules 80 mg | Oral | 1 | .. | MK |\n| --- | --- | --- | --- | --- | --- |\n| \"BCG Immunotherapeutic\" (Bacillus Calmette-Guérin/ Connaught strain) | Single dose set comprising 1 vial powder for intravesical administration containing 6.6 to 19.2 x 108 CFU and 1 vial diluent 3 mL | Intravesical administration | 3 | 1 | AV |\n| \"BCG-Tice\" (Bacillus Calmette-Guérin/Tice strain) | Vial containing powder for intravesical administration approximately 5 x 108 CFU | Intravesical administration | 3 | 1 | OR |\n| Bleomycin Sulfate | Powder for injection 15,000 I.U. | Injection | 10 | .. | BQ, MX, ZH |\n| Calcium Folinate | Tablet equivalent to 15 mg folinic acid | Oral | 10 | .. | MX |\n|  | Injection equivalent to 50 mg folinic acid in 5 mL | Injection | 5 | 5 | MX, PF |\n|  | Injection equivalent to 100 mg folinic acid in 10 mL | Injection | 10 | 1 | PF |\n| Carboplatin | Solution for I.V. injection 50 mg in 5 mL vial | Injection | 2 | .. | MX, PU |\n|  | Solution for I.V. injection 150 mg in 15 mL vial | Injection | 6 | .. | MX, PU |\n|  | Solution for I.V. injection 450 mg in 45 mL vial | Injection | 2 | .. | MX, PU |\n| Cisplatin | I.V. injection 10 mg in 10 mL vial | Injection | 1 | .. | PU |\n|  | I.V. injection 50 mg in 50 mL vial | Injection | 1 | .. | MX, PU |\n|  | I.V. injection 100 mg in 100 mL vial | Injection | 1 | .. | MX |\n| Cladribine | Injection 10 mg in 5 mL vial | Injection | 7 | .. | OA |\n|  | Solution for I.V. infusion 10 mg in 10 mL single use vial | Injection | 7 | .. | JC |\n| Cyclophosphamide | Injection 500 mg (anhydrous), vial | Injection | 2 | .. | BX |\n|  | Injection 1 g (anhydrous), vial | Injection | 1 | .. | BX |\n|  | Injection 2 g (anhydrous), vial | Injection | 1 | .. | BX |\n| Cytarabine | Injection 100 mg in 5 mL vial | Injection | 10 | 1 | PU |\n|  | Injection 500 mg in 5 mL vial | Injection | 2 | 1 | MX |\n| Docetaxel | Injection set containing 1 single use vial concentrate for I.V. infusion 20 mg (anhydrous) in 0.5 mL and 1 single use vial solvent 1.5 mL | Injection | 2 | .. | AV |\n|  | Injection set containing 1 single use vial concentrate for I.V. infusion 80 mg (anhydrous) in 2 mL and 1 single use vial solvent 6 mL | Injection | 1 | .. | AV |\n| Dolasetron Mesylate | Tablet 200 mg | Oral | 2 | .. | AV |\n|  | I.V. injection 100 mg in 5 mL ampoule | Injection | 1 | .. | AV |\n| Doxorubicin Hydrochloride | Solution for I.V. injection or intravesical administration 10 mg in 5 mL single dose vial | Injection or intravesical administration | 4 | .. | IT, MX, PH |\n|  | Solution for I.V. injection or intravesical administration 20 mg in 10 mL single dose vial | Injection or intravesical administration | 4 | .. | PH |\n|  | Solution for I.V. injection or intravesical administration 50 mg in 25 mL single dose vial | Injection or intravesical administration | 3 | .. | IT, MX, PH |\n|  | Solution for I.V. injection or intravesical administration 100 mg in 50 mL single dose vial | Injection or intravesical administration | 1 | .. | IT |\n|  | Solution for I.V. injection or intravesical administration 200 mg in 100 mL single dose vial | Injection or intravesical administration | 1 | .. | IT |\n| Doxorubicin Hydrochloride - Pegylated Liposomal | Suspension for I.V. infusion 20 mg in 10 mL vial | Injection | 1 | .. | SH |\n|  | Suspension for I.V. infusion 50 mg in 25 mL vial | Injection | 1 | .. | SH |\n|  |  |  |  |  |  |\n\n\nColumn 1 Column 2 Column 3 Column 4 Column 5 Column 6\n\nName of chemotherapy Form (strength, type, size, etc.) Manner of  Maximum Maximum Brand\n\npharmaceutical  administration quantity number of\n\n    repeats \n\n    \n\n| Epirubicin Hydrochloride | Solution for injection 10 mg in 5 mL | Injection or intravesical administration | 4 | .. | MX, PH |\n| --- | --- | --- | --- | --- | --- |\n|  | Solution for injection 20 mg in 10 mL | Injection or intravesical administration | 4 | .. | MX, PH |\n|  | Solution for injection 50 mg in 25 mL | Injection or intravesical administration | 3 | .. | MX, PH |\n|  | Solution for injection 100 mg in 50 mL | Injection or intravesical administration | 2 | .. | MX |\n| Etoposide | Solution for I.V. infusion 100 mg in 5 mL vial | Injection | 5 | .. | MX |\n| Etoposide Phosphate | Powder for I.V. infusion 113.6 mg, vial | Injection | 5 | .. | BQ |\n|  | Powder for I.V. infusion 1.136 g, vial | Injection | 1 | .. | BQ |\n| Fluorouracil Sodium | Injection equivalent to 500 mg fluorouracil in 10 mL vial | Injection | 10 | .. | MX |\n| Fotemustine | Powder for injection 208 mg with solvent | Injection | 1 | 4 | SE |\n| Gemcitabine Hydrochloride | Powder for I.V. infusion equivalent to 200 mg gemcitabine | Injection | 4 | 2 | LY |\n|  | Powder for I.V. infusion equivalent to 1 g gemcitabine | Injection | 2 | 2 | LY |\n| Granisetron Hydrochloride | Tablet equivalent to 2 mg granisetron | Oral | 2 | .. | MX |\n|  | Concentrated injection equivalent to 3 mg granisetron in 3 mL ampoule | Injection | 1 | .. | MX |\n| Idarubicin Hydrochloride | Capsule 5 mg | Oral | 3 | .. | PH |\n|  | Capsule 10 mg | Oral | 3 | .. | PH |\n|  | Solution for I.V. injection 5 mg in 5 mL single use vial | Injection | 3 | .. | PH |\n|  | Powder for I.V. injection 5 mg in single dose vial | Injection | 3 | .. | PH |\n|  | Solution for I.V. injection 10 mg in 10 mL single use vial | Injection | 6 | .. | PH |\n|  | Powder for I.V. injection 10 mg in single dose vial | Injection | 6 | .. | PH |\n| Ifosfamide | Powder for I.V. injection 1 g in single dose vial | Injection | 5 | 5 | BX |\n|  | Powder for I.V. injection 2 g in single dose vial | Injection | 5 | 5 | BX |\n| Interferon Alfa-2a | Injection 3,000,000 I.U. in 0.5 mL single dose pre-filled syringe | Injection | 15 | 4 | RO |\n|  | Injection 4,500,000 I.U. in 0.5 mL single dose pre-filled syringe | Injection | 5 | 4 | RO |\n|  | Injection 6,000,000 I.U. in 0.5 mL single dose pre-filled syringe | Injection | 5 | 4 | RO |\n|  | Injection 9,000,000 I.U. in 0.5 mL single dose pre-filled syringe | Injection | 5 | 4 | RO |\n| Interferon Alfa-2b | Solution for injection 18,000,000 I.U. in 1.2 mL multi-dose injection pen | Injection | 3 | 4 | SH |\n|  | Solution for injection 30,000,000 I.U. in 1.2 mL multi-dose injection pen | Injection | 3 | 5 | SH |\n| Irinotecan Hydrochloride Trihydrate | I.V. injection 40 mg in 2 mL vial | Injection | 1 | 3 | MX, PU |\n|  | I.V. injection 100 mg in 5 mL vial | Injection | 2 | 3 | MX, PU |\n| Mesna | Solution for I.V. injection 400 mg in 4 mL ampoule | Injection | 15 | 5 | BX |\n|  | Solution for I.V. injection 1 g in 10 mL ampoule | Injection | 15 | 5 | BX |\n| Methotrexate | Injection 5 mg in 2 mL vial | Injection | 5 | .. | MX |\n|  | Injection 50 mg in 2 mL vial | Injection | 5 | .. | MX, PU |\n|  | Solution concentrate for I.V. infusion   500 mg in 5 mL vial | Injection | 1 | .. | IT |\n\n\nColumn 1 Column 2 Column 3 Column 4 Column 5 Column 6\n\nName of chemotherapy Form (strength, type, size, etc.) Manner of  Maximum Maximum Brand\n\npharmaceutical  administration quantity number of\n\n    repeats \n\n \n\n- Solution concentrate for I.V. infusion 1000 mg in 10 mL vial Injection 1 .. IT\n- Solution concentrate for I.V. infusion 5000 mg in 50 mL vial Injection 1 .. IT\n- Mitozantrone Hydrochloride Injection equivalent to 10 mg mitozantrone in 5 mL vial Injection 1 .. PU\n- Injection equivalent to 20 mg mitozantrone in 10 mL vial Injection 1 .. BX, PU, SI\n- Injection equivalent to 25 mg mitozantrone in 12.5 mL vial Injection 1 .. BX, PU, SI\n- Ondansetron Wafer 4 mg Oral 4 .. GK\n- Wafer 8 mg Oral 4 .. GK\n- Ondansetron Hydrochloride Dihydrate Tablet equivalent to 4 mg ondansetron Oral 4 .. GK\n- Tablet equivalent to 8 mg ondansetron Oral 4 .. GK\n- I.V. injection equivalent to 4 mg ondansetron in 2 mL ampoule Injection 1 .. GK\n- I.V. injection equivalent to 8 mg ondansetron in 4 mL ampoule Injection 1 .. GK\n- Oxaliplatin Powder for I.V. infusion 50 mg, vial Injection 1 2 SW\n- Solution concentrate for I.V. infusion 50 mg in 10 mL vial Injection 1 2 SW\n- Powder for I.V. infusion 100 mg, vial Injection 1 2 SW\n- Solution concentrate for I.V. infusion 100 mg in 20 mL vial Injection 1 2 SW\n- Paclitaxel Solution concentrate for I.V. infusion 30 mg in 5 mL vial Injection 5 .. BQ, IT, MX\n- Solution concentrate for I.V. infusion 100 mg in 16.7 mL vial Injection 2 .. BQ, IT, MX\n- Solution concentrate for I.V. infusion 150 mg in 25 mL vial Injection 2 .. IT, MX\n- Solution concentrate for I.V. infusion 300 mg in 50 mL vial Injection 1 .. BQ, IT, MX\n- Pemetrexed Disodium Heptahydrate Powder for I.V. infusion equivalent to 500 mg pemetrexed, vial Injection 2 2 LY\n- Raltitrexed Powder for I.V. infusion 2 mg in single use vial Injection 3 2 AP\n- Rituximab Solution for I.V. infusion 100 mg in 10 mL vial Injection 2 3 RO\n- Solution for I.V. infusion 500 mg in 50 mL vial Injection 1 3 RO\n- Temozolomide Capsule 5 mg Oral 15 2 SH\n- Capsule 20 mg Oral 15 2 SH\n- Capsule 100 mg Oral 15 2 SH\n- Capsule 250 mg Oral 5 5 SH\n- Thiotepa Injection 15 mg Injection or intravesical administration 2 1 SI\n- Topotecan Hydrochloride Powder for I.V. infusion equivalent to 4 mg topotecan, vial Injection 5 1 GK\n- Tropisetron Hydrochloride Capsule equivalent to 5 mg tropisetron Oral 2 .. NV\n- I.V. injection equivalent to 5 mg tropisetron in 5 mL ampoule Injection 1 .. NV\n- Vinblastine Sulfate Injection 10 mg vial Injection 5 .. AS\n- Solution for I.V. injection 10 mg in 10 mL vial Injection 5 .. MX\n- Vincristine Sulfate I.V. injection 1 mg in 1 mL vial Injection 10 .. MX, PU\n- Vinorelbine Tartrate Solution for I.V. infusion equivalent to 10 mg vinorelbine in 1 mL vial Injection 16 2 FB, MX\n- Solution for I.V. infusion equivalent to 50 mg vinorelbine in 5 mL vial Injection 4 2 FB, MX\n\n\n \n\n \n\nSCHEDULE 3\n\n- Column 1Name ofchemotherapy pharmaceutical Column 2Form (strength, type, size, etc.) Column 3Purposes Column 4Manner ofadmini-stration Column 5Maximum quantity Column 6Maximum number of repeats Column 7Brand\n- Interferon Alfa-2a Injection 3,000,000 I.U. in 0.5 mL single dose pre-filled syringe In compliance with authority procedures set out in paragraph 14: Injection 15 5 RO\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Injection 4,500,000 I.U. in 0.5 mL single dose pre-filled syringe In compliance with authority procedures set out in paragraph 14: Injection 5 5 RO\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Injection 6,000,000 I.U. in 0.5 mL single dose pre-filled syringe In compliance with authority procedures set out in paragraph 14: Injection 5 5 RO\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Injection 9,000,000 I.U. in 0.5 mL single dose pre-filled syringe In compliance with authority procedures set out in paragraph 14: Injection 5 5 RO\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Interferon Alfa-2b Solution for injection 18,000,000 I.U. in 1.2 mL multi-dose injection pen In compliance with authority procedures set out in paragraph 14: Injection 3 5 SH\n- Maintenance treatment of multiple myeloma once remission has been achieved with chemotherapy\n- Low grade non-Hodgkin's lymphoma with clinical features suggestive of a poor prognosis, in combination with anthracycline-based chemotherapy\n- Pemetrexed Disodium Heptahydrate Powder for I.V. infusion equivalent to 500 mg pemetrexed, vial In compliance with authority procedures set out in paragraph 14:Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where treatment with paclitaxel or docetaxel is contraindicated Injection 2 2 LY\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where intolerance to treatment with either docetaxel or paclitaxel has developed\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where treatment with either docetaxel or paclitaxel has been unsuccessful\n- Locally advanced or metastatic non-small cell lung cancer, after prior platinum-based chemotherapy, where transfer to docetaxel or paclitaxel is likely to result in adverse clinical consequences\n\n\n\n\n\n| Column 1Name ofchemotherapy pharmaceutical | Column 2<br>Form (strength, type, size, etc.) | Column 3<br>Purposes | Column 4<br>Manner of<br>admini-<br>stration | Column 5<br>Maximum quantity | Column 6<br>Maximum number of repeats | Column 7<br>Brand |\n| --- | --- | --- | --- | --- | --- | --- |\n| Rituximab | Solution for I.V. infusion 100 mg in 10 mL vial | In compliance with authority procedures set out in paragraph 14: | Injection | 2 | 7 | RO |\n|  |  | Treatment of previously untreated, CD20 positive, diffuse large B-cell non-Hodgkin's lymphoma, in combination with chemotherapy |  |  |  |  |\n|  | Solution for I.V. infusion 500 mg in 50 mL vial | In compliance with authority procedures set out in paragraph 14: | Injection | 1 | 7 | RO |\n|  |  | Treatment of previously untreated, CD20 positive, diffuse large B-cell non-Hodgkin's lymphoma, in combination with chemotherapy |  |  |  |  |\n| Temozolomide | Capsule 5 mg | In compliance with authority procedures set out in paragraph 14: | Oral | 5 | 5 | SH |\n|  |  | Recurrence of anaplastic astrocytoma following standard therapy |  |  |  |  |\n|  |  | Recurrence of glioblastoma multiforme following standard therapy |  |  |  |  |\n|  |  | Glioblastoma multiforme following radiotherapy |  |  |  |  |\n|  | Capsule 20 mg | In compliance with authority procedures set out in paragraph 14: | Oral | 5 | 5 | SH |\n|  |  | Recurrence of anaplastic astrocytoma following standard therapy |  |  |  |  |\n|  |  | Recurrence of glioblastoma multiforme following standard therapy |  |  |  |  |\n|  |  | Glioblastoma multiforme following radiotherapy |  |  |  |  |\n|  | Capsule 100 mg | In compliance with authority procedures set out in paragraph 14: | Oral | 5 | 5 | SH |\n|  |  | Recurrence of anaplastic astrocytoma following standard therapy |  |  |  |  |\n|  |  | Recurrence of glioblastoma multiforme following standard therapy |  |  |  |  |\n|  |  | Glioblastoma multiforme following radiotherapy |  |  |  |  |\n|  |  |  |  |  |  |  |\n\n\n \n\n \n\n \n\nSCHEDULE 4\n\n| Column 1<br>Name of chemotherapy pharmaceutical | Column 2<br>Form (strength, type, size, etc.) | Column 3Brand | Column 4<br>Relevant quantity or number of units | Column 5<br>Manufacturer’s price<br>$ | Column 6<br>Price claimed by manufacturer<br>$ |\n| --- | --- | --- | --- | --- | --- |\n| Bleomycin Sulfate | Powder for injection 15,000 I.U. | MX | 1 | 44.33 | 84.20 |\n|  |  | ZH | 10 | 443.25 | 842.02 |\n|  |  | BQ | 10 | 443.25 | 910.80 |\n| Calcium Folinate | Injection equivalent to 50 mg folinic acid in 5 mL | PF | 10 | 234.80 | 235.01 |\n| Pemetrexed Disodium<br>  Heptahydrate | Powder for I.V. infusion equivalent to 500 mg pemetrexed, vial (unless authorisation is obtained in accordance with paragraph 14 for a purpose specified in column 3 of Schedule 3) | LY | 1 | 1395.59 | 1594.95 |\n|  |  |  |  |  |  |\n\n\n \n","sortOrder":0}],"analysis":{"kimi_summary":{"_metrics":{"model":"kimi-k2.5","source":"moonshot-realtime","completionTokens":2041},"content_quality":"ok","complexity_score":6,"scope_assessment":{"changed":false,"description":"The instrument establishes the Chemotherapy Pharmaceuticals Access Program exactly as described in its title and preamble. Its scope is tightly confined to chemotherapy pharmaceuticals for non-admitted and day patients in public hospitals participating in the Australian Health Care Agreements, with no evidence of scope creep beyond this original purpose."},"complexity_factors":["Four detailed schedules listing specific drugs, forms, brands, quantities and indications with cross-references between Schedules 2 and 3","Extensive cross-referencing to the National Health Act 1953, Health Insurance Act 1973, and Pharmaceutical Benefits Regulations 1960","Authority approval system requiring electronic interaction with the 'HIC authority notification computer system' for restricted items","Brand-specific restrictions tied to manufacturer codes (e.g., 'LY', 'RO') limiting supply to specific pharmaceutical companies","Dual scheduling mechanism (Schedules 2 and 3) with different rules for maximum quantities, repeats and authority requirements","Complex charging provisions calculating patient co-payments and manufacturer price differentials under Schedule 4"],"plain_english_summary":"The instrument creates the Chemotherapy Pharmaceuticals Access Program, letting public hospitals supply subsidised chemotherapy and related medicines to non-admitted patients (outpatients, day patients, and recently discharged). It specifies approved drugs, brands and strengths, uses a hospital medication chart as the legal prescription, and requires prior HIC approval for certain high-cost items. Patients pay PBS-style co‑payments (plus extra for some drugs); the Commonwealth reimburses hospitals the remainder, ensuring affordable access to essential cancer treatment."}},"importantCases":[],"_links":{"self":"/api/acts/f2005l02120","history":"/api/acts/f2005l02120/history","analysis":"/api/acts/f2005l02120/analysis","conflicts":"/api/acts/f2005l02120/conflicts","importantCases":"/api/acts/f2005l02120/important-cases","documents":"/api/acts/f2005l02120/documents"}}