Vol 23- May 2009
 
Increased medicines funding expected in May Budget
  Since the establishment of PHARMAC in 1993, pharmaceutical expenditure has averaged a growth of just 2% per year, less than the average rate of inflation said an OECD report Healthcare Reform: Challenges for the Next Phase which was released in April.
  This report was highly supportive of PHARMAC but warned that if Government really wishes to fund expensive new drugs it should expand PHARMAC’s budget and not interfere in its decision making.
  Clinicians and patients alike are awaiting a promised ‘substantial’ increase in funding expected in the May Budget.  According to a political column in the NZ Doctor Health Minister, Hon Tony Ryall has indicated that the increase would widen the scope of the medicines PHARMAC could buy. 
  National promised a $180m increase over three years in the election campaign and Mr Ryall is quoted as suggesting that previous increases “certainly didn’t keep up with population growth. 
  “The new Government’s plan is to move to catch up with population growth over the next three years,” he is reported to have said.
  However, the promised increase of $180m might not be quite what people are expecting as we understand that it will come off a fixed base. The increase in funding in years one, two and three would not be an additional $40m, $60m and $80m in each of the respective years, but rather an increase of $40m, $20m and $20m of additional funding in each of the three years. 

Apology
  The RMI apologises for an error in the graph in the last e-zine.  In the last issue of this newsletter we incorrectly depicted the 2008/09 community schedule budget as $533m, instead of $653m.  The correction is in the graph below which illustrates the effect of a three year budget increase calculated from a flat base.

Additional funding for medicines
 
Counterfeit medicines, a growing concern
  According to the World Health Organisation more than 50% of medicines purchased on internet sites without a physical address are counterfeit.
  It also says that between 6% and 10% of medicines on the world market are reported to be counterfeit with estimated sales of over US $35 billion a year. The problem is most serious in developing countries.
  The 61st World Health Assembly considered a report on counterfeit medical products in May last year, but has been unable to reach agreement on an international approach to the problem.
  Meanwhile the problem grows.  Counterfeit medicines are potentially extremely dangerous, with no controls over what they contain.  Chilling stories about the risks associated with counterfeit medicines are becoming more and more common.
  New Zealand is not immune to the growing problem which is an additional burden to already hard working border control officials both here and overseas. 
  For instance, the United Kingdom’s Medicines and Healthcare products Regulatory Agency (MHRA) seized nearly half a million pounds worth of counterfeit medicines in March this year in Middlesbrough, England.
  In the US a PhRMA survey found that a significant number of American adults had recently purchased medicines from a foreign country. Half of those surveyed are buying their drugs in another country because they lack a doctor’s prescription. What’s more, the survey found that antibiotics and pain relief medicines are, in most cases, the typical medications American consumers seek from other countries.
  The Australian regulator, TGA, has issued a public warning over imports of counterfeit medicines into Australia.  It says that, over recent months, there has been an increase in the personal importation of lifestyle products claiming to contain only herbal ingredients but actually including pharmaceutical actives.
  “Regulators in developed countries, such as Medsafe here in New Zealand, ensure that medicines prescribed by clinicians and dispensed by pharmacists are safe, effective and high quality products.  Counterfeit products purchased over the internet have no such safety evaluation and should be avoided,” said Ken Shirley, the CEO of the Researched Medicines Industry Association.
  Read more about the problems with counterfeit medicines here  www.BuySafeDrugs.info
 

 
This newsletter is published on behalf of the
Researched Medicines Industry Association of New Zealand. The views and opinions expressed in this publication are not necessarily those of the RMI.


For further information:

Researched Medicines Industry Association
PO Box 10447 Wellington
Phone 04 499 4277
http://www.rmianz.co.nz


  
Pharmacoeconomics seminar
  Some 25 representatives of RMI member companies attended a PHARMAC presentation in Auckland on Friday 24th April outlining the details of cost utility analysis (CUA) – why it is used and how it is done.
  A commonly expressed industry concern was the lack of transparency in the processes associated with determining priorities for the funding of medicines.  It was also acknowledged that any new investment in pharmaceuticals is subject to an extremely stringent evaluation compared with other investments in the health sector.

Parliamentary examination of PHARMAC
  The pharmaceutical schedule was under spent again over the 2007-08 financial year, by $400,000 Parliament’s Health Select Committee was told in late March. 
  “While this is a foregone opportunity in pharmaceutical investment, it must be pointed out that it represents a mere 0.06% of the total community schedule budget.  It would seem that greater flexibility and a carry-over provision would be the only way of ensuring that the full amount of money budgeted by DHBs for medicines is spent on those items,” the RMI CEO, Ken Shirley, commented.
  The Select Committee was also told by Pharmac CEO Matthew Brougham that it has two current key challenges; the public acceptance of generics and the increasing cost of some new medicines.

Cure for cancer in our time?
  In an address to Congress President Obama called for “a cure for cancer in our time” as a key initiative during his presidency.  He would therefore have been pleased to see a March pharmaceutical industry report on medicines in the research pipeline for cancer.  It shows that the US’s pharmaceutical research and biotechnology companies are testing a record 861 new cancer medicines and vaccines.  These medicines are all now either in clinical trials or awaiting approval by the USFDA.
 
The medicines represent many cutting-edge approaches, including a drug that delivers a synthetic version of a substance derived from scorpions directly to brain tumour cells, a number of cancer vaccines, medicines that target and kill specific cancer cells and treatments that activate the patient’s general immune system to destroy cancer. 
 
To access the report, click here.   
 

 

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