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16 Cards in this Set

  • Front
  • Back
General mechanism
a) inactivate Na+ channels
b) promote GABA inhibition
Phenobarbital
barbiturate/anticonvulsant. Engage GABA,
delay Cl- channel closure. Raise firing threshold
-Sedation and nystagmus
Phenytoin
slow recovery of Na+ channels from inactive state
-Gingival hyperplasia, hyperglycemia, osteomalacia, drowsiness
-Hepatic necrosis, nystagmus, diplopia, hypersensitivity rxn, rashes
-CYP2C9/10 and 19
-Interactions with oral contraceptives, warfarin
Carbamazepine
blocks Na+ channels
-For trigeminal neuralgia
-Causes aplastic anemia
Ethosuximide
blocks t-type Ca++ current in thalamic neurons, nonconvulsive seizures
-Hiccups
Trimethadione
blocks t-type ca++ currents, for nonconvulsive seizures
Valproic acid/divalproex
fatty acid with anticonvulsant properties. All types of epilepsy
-Fatal hepatitis
Gabapentin
analogue of GABA. Block N-type Ca++ channels? Decrease synaptic release of glu
Topiramate
monosaccharide. Block Na+ channels, hyperpolarize via K+ current
Felbamate
partial seizures, potentiate GABA, block NMDA receptor
-Aplastic anemia and hepatitis
Lamotrigine
adjunct, inactivate Na+ channels
Tiagabine
inhibits GABA transporter GAT-1 (reuptake)
Zonisamide
sulfanomide derivative, block of Na+ and voltage gated Ca++ channels, inhibits CA
Levetiracetam
partial seizures, binds to SV2A to modify GABA/glu release. No interation with P450
Acetazolamide
inhibit CA (also diuretic)
Diazepam
used to treat status epilepticus