GlaxoSmithKlineThe Impact of Medicines: Sustainability in Environment, Health and Safety Report 2002
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About this report

Executive statements

Framework

Issues

Designing products for environmental sustainability

Ozone depletion

Pharmaceuticals in the environment

Biodiversity

Genetically modified organisms

Contaminated land

Occupational hazard evaluation and use of animals

Performance

Verification statement

Index

Ozone depletion
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GSK is taking significant steps to eliminate any ozone depleting impact arising from our processes, products and operations. We have a target to eliminate use of ozone depleting compounds in refrigeration and air conditioning equipment by substituting materials that do not deplete ozone. We are also working to reduce the environmental impact from the manufacture and use of our asthma and chronic obstructive pulmonary disease (COPD) medications.

Asthma medication and the environment
Asthma is a chronic and life threatening disease that affects 300 million people around the world. It is a disease of chronic inflammation and bronchoconstriction with symptoms such as cough, wheezing and chest tightness. Asthma prevalence is increasing. In developed countries it currently affects 10% of children and 5% of adults. In developing countries like Brazil, Peru and Uruguay the prevalence of asthma is estimated to be between 20 and 30 percent of the population. Asthma and COPD are linked to over 1,700 deaths per year in the UK.

Metered Dose Inhalers (MDIs) are one of the main forms of treatment for asthma. MDIs were first introduced in the 1950s. The MDI is a pocket-sized, hand-held, pressurised multiple dose inhalation system that can deliver a precise dose of medication to the airways when used appropriately. Essential components of an MDI are a canister, the drug substance, a gas to propel the drug into the patient and a device for releasing and directing the dose.

For decades, CFCs were the most suitable propellant for use in MDIs because they are non-toxic, non-reactive, non-flammable, odour and taste free and excellent solvents. However, CFCs have now been recognised as ozone depleting and global warming gases.

In recognition of their importance in the fight against asthma and COPD, the production of CFCs to manufacture MDIs in the developed world has been deemed as an 'essential use' under the Montreal Protocol, until adequate alternatives to CFC-containing medications are available. Each year GlaxoSmithKline applies for volumes of CFC to be used to manufacture our MDIs under this 'essential use' exemption. GSK's requested volumes have recently been declining each year and GSK will soon no longer need to request any essential-use volumes. GSK takes the issue of ozone depletion seriously and supports the objectives of the Montreal Protocol. We believe that the Parties to the Protocol should now move to adopt a decision that, with due notice, phases down and closes the essential use exemption for MDIs for developed countries. Such a Protocol decision should include strong interim measures to significantly reduce volumes of CFCs used for MDI manufacture after 2005.

GSK offers a wide range of options for the treatment of respiratory disease including MDIs, dry powder devices and liquids for use in nebulisers. We have done extensive research into developing replacements for the CFC propellants and have reformulated the majority of our MDI products to use the non-ozone depleting gas HFC 134a. In 2002 GSK manufactured over one hundred million non-CFC MDIs and launched our first non-CFC MDI in the US namely, CFC-free Ventolin.

GSK is taking steps to reduce the ozone depleting impact arising from our processes, products and operations by:

  • Reformulating the propellant in the MDIs from CFCs to HFC 134a, a non-ozone depleting replacement.
  • Minimising emissions arising from MDIs rejected during the manufacturing stage in accordance with national standards.
  • Launching globally the non-CFC MDI as soon as possible after obtaining regulatory approval.
  • Removing the corresponding CFC product from the market within 6-12 months of launch depending on individual country health practices.
  • Offering a choice of an MDI or DPI (dry powder inhaler) device for our respiratory drugs.
  • Continuing to invest in research & development of novel inhaler devices with even lower environmental impacts.
  • Minimising fugitive emissions of CFCs and other ozone depleting gases from our manufacturing sites through engineering controls and replacing halons (fire fighting gases) and refrigerants.

GSK also takes the issue of climate change seriously and supports the objectives of the Kyoto Protocol. Although some uncertainties remain, we believe that the potential global significance of climate change is too serious to ignore and that, under the precautionary principle, it warrants a measured global response. Even though the HFC 134a MDI propellant is a recognised greenhouse gas, GSK believes that in the interests of public health, as there is no real alternative for many active ingredients, the small and critically important medical use of HFCs in MDIs deserves special safeguards in international and national climate change strategies.

However, we will continue to pursue options that employ compounds that don't have an adverse impact to the environment.

Read about our management of ozone depleting substances



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