Does anyone feel if one of the two drugs that make-up Qnexa wasn't generic the advisory panel would have voted differently?
Considering phentermine and topiramate are currently being used widely off-label. Price and finding the right doctor seem to be the only limiting factors. Cheap and easy access, along with increasing public awareness of off-label use, might force the FDA's hand towards approval instead of prudently asking for further testing. The REM strategy beats unchecked usage in an off-label market growing exponentially.
Does anyone feel if one of the two drugs that make-up Qnexa wasn't generic the advisory panel would have voted differently?
If Qnexa were a novel drug, I think the panel’s sentiment would have been considerably different and might well have produced a plurality of negative votes.