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United Kingdom · Motion · Early Day Motion

EDM 535

INSULIN TREATMENTS

openUnited Kingdom· UK Parliament· EN

Introduced

18 December 2006

Last action

18 December 2006 · Early Day Motion

Status

0

Sponsors

Sandra Gidley

Subjects

Discovery layer

Source updated

18 December 2006

Summary

That this House congratulates Wockhardt Pharmaceuticals on the expansion of production facilities for animal insulins to cope with increased demand as a result of Novo Nordisk Pharmaceutical's discontinuation of their pork insulin and thanks the Minister of State, the hon. Member for Leigh, for his Department's role in ensuring that animal insulins continue to be available for those people who need them, but regrets that Novo Nordisk Pharmaceuticals has begun a systematic discontinuation of their synthetic `human' insulin products in favour of insulin analogues, further reducing patient and physician choice; expresses grave reservations that many patients are being transferred to insulin analogues before their long-term safety has been established and before studies recommended by the European Agency for the Evaluation of Medical Products have been carried out to investigate the potential for carcinogenic effects of insulin analogues; and therefore requests that the Secretary of State for Health asks the National Institute for Health and Clinical Excellence to assess the safety, clinical and cost effectiveness of all insulins to provide patients and clinicians with the necessary information to make informed treatment choices.

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Timeline

  1. 18 December 2006

    Early Day Motion

    That this House congratulates Wockhardt Pharmaceuticals on the expansion of production facilities for animal insulins to cope with increased demand as a result of Novo Nordisk Pharmaceutical's discontinuation of their pork insulin and thanks the Minister of State, the hon. Member for Leigh, for his Department's role in ensuring that animal insulins continue to be available for those people who need them, but regrets that Novo Nordisk Pharmaceuticals has begun a systematic discontinuation of their synthetic `human' insulin products in favour of insulin analogues, further reducing patient and physician choice; expresses grave reservations that many patients are being transferred to insulin analogues before their long-term safety has been established and before studies recommended by the European Agency for the Evaluation of Medical Products have been carried out to investigate the potential for carcinogenic effects of insulin analogues; and therefore requests that the Secretary of State for Health asks the National Institute for Health and Clinical Excellence to assess the safety, clinical and cost effectiveness of all insulins to provide patients and clinicians with the necessary information to make informed treatment choices.

    Source: Early Day Motion

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