Thursday, January 21, 2010

Reductil (sibutramine) pulled from the EU market

The anti-obesity drug sibutramine has had its licence suspended by the European authorities due to concerns over an increased risk of cardiovascular events with the treatment.

The Medicines and Healthcare products Regulatory Agency announced today that a European-wide review had concluded the risk of heart attacks and strokes from sibutramine (Reductil) outweighs the benefit gained from weight loss.

NHS data show GPs issued over 330,000 prescriptions for sibutramine in 2008, but GPs have been advised not to issue any new prescriptions for sibutramine and to review the treatment of any patients taking the drug.

Both the European Medicines Agency and the US Food and Drug Administration announced reviews into sibutramine last December after a study found an excess of serious cardiovascular events in high-risk patients on the treatment.

Dr June Raine, director of vigilance and risk management of medicines at the MHRA said: 'Evidence suggests that there is an increased risk of non-fatal heart attacks and strokes with this medicine that outweigh the benefits of weight loss, which is modest and may not be sustained in the long term after stopping treatment.

'Prescribers are advised not to issue any new prescriptions for Reductil and to review the treatment of patients taking the drug.

1 comment:

fergi said...

Hi There,

Please can people share their experience with Reductil here;

http://reductilvictim.blogspot.com