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It takes two to tango: ethical dilemmas of health professionals and the therapeutic goods industry Dr Ken Harvey MB BS, FRCPA

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Presentation on theme: "It takes two to tango: ethical dilemmas of health professionals and the therapeutic goods industry Dr Ken Harvey MB BS, FRCPA"— Presentation transcript:

1 It takes two to tango: ethical dilemmas of health professionals and the therapeutic goods industry Dr Ken Harvey MB BS, FRCPA AMSA GHC, Hobart, September 12-15, 2013

2 Talk outline Disclosure of interests Snapshot of current issues WHO resolutions and QUM policy Self-regulatory Codes – Pros and cons Unethical behaviour that led to: – U.S. Physicians Payment Sunshine Act – Therapeutic Goods Amendment (Pharmaceutical Transparency) Bill 2013 – Medicines Australia current Code revision – AHPRA Code of Conduct Conclusion: It takes two to tango. 2 A fundamental change in the relationship between industry and medical professionals is needed.

3 Disclosure of interests Member: – WHO Ethical Criteria for medicinal drug promotion. – Therapeutic Guidelines Limited. – PHARM Committee that devised the Quality Use of Medicines plank of Australian Medicines Policy. Consumer rep (Choice, CHF): – Government Working Group on Promotion of Therapeutic Products. – TGA Transparency Review Panel. – TGA Working Group on Regulatory Framework for Complementary Medicines. – Government Natural Therapy Review Advisory Committee.

4 Mea culpa: are multi-billion dollar fines forcing drug companies to clean up their act? BMJ 2012; 345 (Published 18 July 2012) Snapshots of current issues How Drug Company Money Is Undermining Science November 21, 2012 The pharmaceutical industry funnels money to prominent scientists who are doing research that affects its products--and nobody can stop it

5 World Health Assembly 2007 Resolution 60.16: –Wishing to promote evidence-based rational use of medicines by providers and consumers; URGES Member States to: –Develop and implement programmes that will provide independent, non-promotional information about medicines; –Enact new, or enforce existing, legislation to ban inaccurate, misleading or unethical promotion of medicines; –Monitor promotion. 5

6 Strategies Policy development and implementation National facilitation and co- ordination Independent objective information Ethical behaviour Education and training Interventions Evaluation Quality Use of Medicines Policy 6

7 Independent objective information Prescription medicines 7

8 Independent objective information Prescription medicines 8 Bad research rising: The 7th Olympiad of research on biomedical publication By Hilda Bastian | September 8, 2013

9 Ethical behaviour 9 There is an integrated three-tier system of controls for the advertising of therapeutic goods in Australia. – Self-regulation (promotion to health professionals) Industry Codes and complaints panels in nine sectors: Medicines Australia, GMIA, ASMI, CHC, MTAA, AusBioTech, IVD Australia, ADA, ACCORD. Medical Board and health professional Codes. – Co-regulation (promotion to consumers) Therapeutic Goods Advertising Code (TGAC), Complaints Resolution Panel (CRP) and TGA. – Regulation (legislation) Therapeutic Goods Act 1989 (TGA) and Trade Practices Act, 1974 now renamed the Competition and Consumer Act 2010 (ACCC).

10 Self-regulation: Pros The Australian Governments preference is to maintain an emphasis on self-regulation. TGA reforms: A blueprint for TGAs future. December 2011. 10 The government does not pay the cost (however, the cost to industry is passed on to consumers regardless); May be more flexible and less intrusive than government legislation / regulation; Ownership of a code may produce a stronger commitment for members to comply; Complaint handling procedures under a self-regulatory code can be more cost effective, time efficient and user friendly in resolving complaints than government bodies.

11 Self-regulation: Cons There are nine therapeutic goods industry self-regulatory codes 11

12 Self-regulation: Cons Code content, monitoring, complaint procedures and transparency vary across industry sectors (not a level playing field). Codes often lag behind consumer and health practitioner views due to the absence of external stakeholders. Codes also lag behind the views of more progressive companies because of the need for revisions to be approved by a majority of member companies. Codes don't apply to non-members; a major problem in some sectors of the therapeutic goods industry. Numerous sector based industry Codes make it difficult to know where to send complaints. 12

13 Following media stories about a Sigma cruise and unethical conduct by medical device sponsors Parliamentary Secretary for Health Mark Butler said: – The Government is pursuing a level playing field on marketing obligations within the therapeutic goods industry. 13 Self-regulation: Cons

14 2010 Working Group on promotion 14

15 One Code, one efficient complaint (and appeal) system and one set of effective sanctions applicable to all therapeutic claims and promotional activities regardless of the industry sector, media or target. 15 What many advocated

16 16 Administered by an independent Therapeutic Goods Promotion Agency (TGPA). TGA product registration and listing dependent upon compliance. Escalating pyramid of action. What many advocated 16 Rejercted by industry!

17 2010 Working Group Report Working Group on Promotion of Therapeutic Products (to health professionals) delivered its report to the then Parliamentary Secretary for Health Catherine King on 18 March 2011. It recommended a high level statement of principle: – the Australian therapeutic products industry promotes the concept of good health incorporating the quality use of therapeutic products based on genuine consumer health needs and supported by the ethical conduct of all parties. Common coverage of operational areas, such as industry- sponsored educational events, conduct of representatives, hospitality and entertainment, and social media. 17

18 2010 Working Group Report Common governance areas for effective implementation: – Education on the codes operation; – Monitoring of compliance with the code; – Enforcement of the code in response to a complaint or a breach; – Sanctions to support the enforcement (at a level that deters non-compliance). The government make compliance with a Code a condition of market authorisation (to address the problem of non-members). The latter was rejected by government which preferred voluntary compliance! 18

19 Evaluating voluntary Code sign-up Kate Lynch (CEO, GMiA) noted: GMiA already provides an option for non- members to voluntarily sign up to the GMiA Code without joining the association. Despite pro-actively advocating this facility no company has taken up the option. Non-members have stated that they already adhere to the Code and do not see a need to make any formal declaration. 19

20 Evaluating voluntary Code sign-up In 2012, Ranbaxy Australia offered pharmacists A$14,648 of free Trovas® (generic atorvastatin) stock and a 90% discount for subsequent orders. This offer appeared to breach the Code of Conduct of both the Generic Medicines Industry Association (GMiA) and Medicines Australia. Ranbaxy Australia Pty Ltd is not a member of any self-regulatory industry association. 20

21 Evaluating voluntary Code sign-up 21

22 2013-16 Codes of Conduct Advisory Group Contains representatives from industry associations, health professional and consumer organisations together with DoHA responsible for: – an independent review of the uptake of the 2010 Working Groups high level principles; – development of shared information systems and a common complaints portal; – alignment of industry and health professional codes; – mechanisms to improve the coverage of codes of conduct; – an independent evaluation of the effectiveness of the overall self-regulatory framework; – A budget of $1.4 million from 2012-16. Chair: Prof Lloyd Samson 22

23 Are self-regulatory Codes effective? Medicines Australia maximum fine for a severe breach of their Code is $300,000 (with an average fine around $50,000). This stands in stark contrast to the recent GSK fine of $3 billion by the U.S. Justice Department – which also included GSK entering into a five-year Corporate Integrity Agreement which stipulated major changes to the way the company does business and further penalties for non-compliance). Over the last 5 years settlements for criminal and civil monetary penalties from the U.S. pharmaceutical industry reached a total of $15 billion. 23

24 U.S. Justice Department Fines 24

25 Unethical conduct Trials manipulated; negative results suppressed. Journal articles ghost-written. Off-label promotion. Well paid, but undeclared, medical opinion leaders used to promote company products (educational mercenaries). Excessive hospitality, kickbacks, bribery. Consumer groups manipulated. Spurious patents and legal challenges to delay the entry of generics. 25

26 It takes two to tango 26

27 The need for disclosure A recent editorial in the British Medical Journal reported that a US Senate Finance Committee investigation has found the medical device company Medtronic was heavily involved in drafting, editing, and shaping the content of medical journal articles authored by its physician consultants, who were paid hundreds of millions of dollars by the company through royalties and consulting fees. The Committee Chairman, Senator Max Baucus, said Medtronics actions had violated patients trust. The president of the North American Spine Society, said, If surgeons had known that the lead authors of the 13 original studies on InFuse (the Medtronic product) had received payments ranging from $1.7m to $64m from Medtronic and that its marketing employees were co-authors and co-editors, would they have been as eager to use this product on their patients? 27

28 In the USA The Physician Payment Sunshine Act becomes operational this year. It requires pharmaceutical and device companies to report to the Centers for Medicare and Medicaid Services (CMS) all payments, or other transfers of value, made to individual doctors and teaching hospitals that total more than US$100 per year. Companies must begin to collect the information by August 1, 2013 and report it to the CMS by March 31, 2014. The information will be posted on a public website on 30 September 2014. 28

29 In Australia Many consumer and health professional groups argued for full disclosure of payments made to individual healthcare professionals in the 16th Edition (2009) Code revision and again in the 17th Edition (2012) Code revision. The 17th Code Edition incorporated aggregate disclosure of payments, not individual. MA set up a Transparency Working Group to advise how individual disclosure might be implemented. A report has now been produced but there was no agreement on the amount of money that would trigger individual disclosure. Consultation with MA members and other stakeholders will continue with (hopefully) the adoption of individual payment disclosure in new Code revision in late 2014 with possibly payments being recorded from Jan 1, 2015 and public reporting in 2016 (compared to 2014 in the U.S.). 29

30 In Australia This bill proposed by Senator R Di Natale would have replaced Medicines Australia Code with legislation that set stringent restrictions on the interactions between pharmaceutical companies and physicians. In June 2013, the Finance and Public Administration Legislation Committee recommended that the bill not be passed. Unlike the U.S., self-regulation was thought to be more appropriate in Australia. 30

31 MA Code review 31 There will soon be a call for submissions on the options in discussion paper and also forums where all stakeholders (including AMSA) may come together and discuss the transparency model.

32 New transparency a huge burden? The number of individual HCP reports that companies will have to gather in order to comply with MA's new transparency regime could far exceed 500,000 a year, research by Pharma-in- Focus has shown (with a trigger point of $10 and $100 reporting threshold). A higher trigger point of $25 (favoured by companies) that presented to the MA transparency working group, would cut the numbers by about 50%. 19 August 2013

33 8.11.4Recognising that pharmaceutical and other medical marketing influences doctors, and being aware of ways in which your practice may be being influenced. 8.11.5Recognising potential conflicts of interest in relation to medical devices and appropriately managing any conflict that arises in your practice. 8.11.6Not asking for or accepting any inducement, gift or hospitality of more than trivial value, from companies that sell or market drugs or appliances that may affect, or be seen to affect, the way you prescribe for, treat or refer patients. 8.11.8Not offering inducements to colleagues, or entering into arrangements that could be perceived to provide inducements. 33 AHPRA code of conduct for doctors in Australia

34 Monitoring promotion 34

35 It takes two to tango 35

36 36 The Pharma Phacts Pledge I pledge to accept no money, gifts, or hospitality from the pharmaceutical industry; to seek unbiased sources of information and not rely on information disseminated by drug companies; and to avoid conflicts of interest in my medical education and practice. It takes two to tango

37 In conclusion: One book to read 37

38 In conclusion: Organisations to join Health Action International – Healthy Skepticism – Friends of Science and Medicine – Choice Consumer Action – action.aspx action.aspx 38

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