I recently started a transdermal cycle of 1T and 4ad (200mg/400mg respectively, split morning and night) however I had to give up after just 3 applications. About 10-20 minutes after each application I started feeling like crap, really light headed, spaced out and a little nauseous. Had to lie down for a couple of hours after the third application.
Since it occurred so quickly after application I assumed it must be a reaction to the transport matrix rather than the PHs themselves, does this sound right? Any ideas what it could be?
If I can't take them transdermally will there be any disadvantages to taking them orally, other than being less efficient?
Thanks for your advice