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Class 1 drug alert issued for Xigris (drotrecogin alfa) 5mg and 20mg powder for infusion
The Medicines and Health products Regulatory Agency (MHRA) has issued a class 1 drug alert for Xigris (drotrecogin alfa) 5mg and 20mg powder for infusion (Eli Lilly and Co Ltd). Click here for further details of the alert.
This alert has been issued because new clinical trial findings show a lack of efficacy and call into question the risk-benefit profile of Xigris powder for infusion.
Patients currently being treated with the medicine should discontinue treatment. Pharmacists should return any unused stock to the distributor. We understand this is a hospital-only product not likely to be used by community pharmacists or general practitioners.
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