March 2nd, 2011
FDA Finds No Increased Risk For MI With Abacavir
Larry Husten, PHD
An ongoing safety review by the FDA of the antiviral medication abacavir found no evidence for an increased risk for MI associated with the drug. The FDA said an increased risk for MI with abacavir had been seen in several observational studies and one randomized controlled trial (RCT), but not in other RCTs or in the drug’s safety database. The FDA therefore conducted a meta-analysis of 26 RCTs and found no evidence for an increased risk for MI associated with the drug.