Exactly how carbamazepine works is not known, but it reduces the abnormal electrical activity in the brain that drives seizures. In animal studies, it dampens signals passed along chains of nerve cells and blocks the extra strengthening of signals that follows a burst of rapid firing. For trigeminal neuralgia, it changes the way the body senses pain, and in animals it greatly reduces pain from stimulating a nerve in the face. The liver, mainly through an enzyme called CYP3A4, turns it into carbamazepine epoxide, a breakdown product that also blocks seizures in animals.
With regular tablets, blood levels peak about 4 to 5 hours after a dose, compared with about 1.5 hours for the liquid and 3 to 12 hours for the long-acting tablets. It speeds up its own breakdown over the first 3 to 5 weeks, so the time it stays in the body shortens from 25 to 65 hours at first to about 12 to 17 hours. It also speeds the breakdown of many other medicines, such as hormonal birth control, which can then work less well. Its mild anticholinergic action, which blocks some nerve signals that use acetylcholine, can raise pressure inside the eye, and dizziness, drowsiness, and unsteadiness are most common early on.