Felypressin (FEL), a synthetic analogue of vasopressin (AVP), has been widely used as a substitute for epinephrine (EPI) in anesthetic solutions to promote local vasoconstriction during medical and dental practices. 1 , 2 Because it has no interaction with adrenergic receptors, it is suggested that FEL has fewer side effects than EPI. 3 Hence, FEL causes fewer cardiovascular 4 and metabolic 5 side effects, and it has a higher median lethal dose (LD50) 6 than EPI. However, the mechanisms and the receptors used by FEL to induce