| Question |
Answer |
| MOA phenytoin |
Increases Na channel inactivation |
| MOA carbamazepine |
Increases Na channel inactivation |
| MOA lamotrigine |
blocks voltage gated Na channels |
| MOA gabapentin |
increases GABA release |
| MOA topiramate |
Blocks Na channels, increases GABA release |
| MOA phenobarbital |
increases GABA |
| MOA valproic acid |
increases GABA, blocks Na channels |
| MOA ethosuxamide |
blocks ca channels in thalamus |
| MOA benzos |
increases GABA |
| uses for phenytoin |
everything but absence seizures. status epilepticus prophylaxis |
| usees for lamotrigine |
everything but absence and status |
| uses for carbamazepine |
everything but absence and status |
| uses for gabapentin |
all seizures except absence and status peripheral neuropathy |
| uses for topirimate |
everything but absence and status |
| uses for phenobarbital |
everything but absence and status |
| uses for valproic acid |
everything but status |
| uses for ethosuxamide |
absence |
| uses for benzos in epilepsy |
acute status |
| which anti-epileptic drugs are 1st line in pregnancy and children |
phenobarbital |
| which epi drug is 1st line for trigeminal neuralgia |
carbamazepine |
| which drug is used to treat peripheral neuropathy |
gabapentin |
| which drug is used to treat myoclonic seizures |
valproic acid |
| which drug is used to treat seizures in eclampsia |
MgSO4 (1st line) benzos |
| which epileptic drug --> sedation, tolerance, and dependence? |
benzos |
| which epileptic drug --> aplastic anemia, liver toxicity, and teratogenesis? |
carbamazepine |
| which epileptic drug --> diplopia, ataxia? |
carbamazepine phenytoin |
| which epileptic drug --> GI distress, lethargy, headache? |
ethosuxamide |
| which epileptic drugs --> stevens johnson syndrome |
ethosuxamide lamotragine |
| which epileptic drug --> nystagmus, gingival hyperplasia, hirsutism? |
phenytoin |
| which epileptic drug --> SLE like sydnrome |
phenytoin |
| which epi drug --> spina bifida and other NTDs |
valproic acid |
| which epi drug --> kidney stones |
topiramate |
| which epilepsy drug --> malignant hyperthermia? |
phenytoin |
| how do you treat OD of barbiturates? |
symptom management |
| how do you treat OD of benzos? |
flumazenil (competitive antagonist at GABA receptor) |
| other than for epilepsy, what can phenytoin be used for? |
anti-arrhythmic |
| which is more dangerous in overdose: benzos or barbiturates? |
barbiturates (longer t1/2 and more respiratory/cv depression) |
| MOA l-dopa |
l dopa crosses bbb (dopamine doesn't) so it is converted to dopamine by dopa decarboxylase in CNS |
| carbidopa |
peripheral decarboxylase inhibitor in order to increase bioavailability in brain and decrease peripheral side effects (since the conversion to dopamine won't occur peripherally) |
| toxicity of l-dopa? |
arrhythmias from peripheral conversion of DA dyskinesia following lt admin akinesia between doses |
| MOA selegiline |
selectively inhibits MAO-B, increasing availability of DA |
| use of selegiline |
adjunctive to l-dopa in parkinsons |
| toxicityy of selegeliene |
enhances l-dopa toxicity |
| MOA sumatriptan |
5-HT1D agonist --> vasoconstriction |
| use of sumatriptan |
acute migraine cluster headache attacks |
| what type of drug is bethanechol? |
direct cholinergic agonist |
| what type of drug is carbechol |
direct cholinergic agonist |
| what type of drug is pilocarpine |
direct cholinergic agonist |
| what type of drug is methacholine |
direct cholinergic agonist |
| what is the difference between direct cholinergic agonsts and indirect? |
direct directly stimulate cholinergic receptors and indirect inhibit their breakdown via AChE |
| uses of bethanechol |
activates bladder and bowel smooth muscle (used post-op for ileus and urinary retention) |
| uses of carbechol |
glaucoma pupillary contraction release of intraocular pressure |
| uses of pilocarpine |
potent stimulator for saliva, sweat, and tears |
| uses of methacholine |
challenge test for asthma dx |
| action of methacholine |
stimulates muscarinic receptors in airway |
| class: neostigmine |
indirect cholinomimetic |
| class pyrodostigmine |
indirect cholinomimetic |
| class: edrophonium |
indirect cholinomimetic |
| class: physostigmine |
indirect cholinomimetic |
| class: echothiophate |
indirect cholinomimetic |
| uses for neostigmine |
post-op and neurogenic ileus and uriNAry retention MG reversal of NM junction blockade |
| uses for pyridostigmine |
MG |
| uses for edrophonium |
to dx MG |
| uses for physostigmine |
glaucoma and atropine OD |
| uses for echothiophate |
glaucoma |
| which indirect ACh agonist penetrates CNS |
physostigmine |