There are two products forming. The peak on the left is a non-specific product or a primer-dimer. In other words the PCR is not working exactly as you were hoping it would, and it is making a second PCR product. The quantitation of product from such a reaction will be artificially high since the non-specific product will be quantified along with the specific product. Assuming you are already using standard QPCR conditions I suggest you redesign the primers.