Neurology Flashcards
Morphine, fentanyl, codine, loperamide, methadone, meperidine, dextromethorphan, diphenoxylate (MOA)
Agonist at opioid receptors (mu=morphine, delta=enkephaline, kappa=dynorphin) to modulate synaptic transmission - open K channels, close Ca channels -> decreased synaptic transmission. Inhibit release of ACh, norepinephrine, 5-HT, glutamate, substance P.
Morphine, fentanyl, codine, loperamide, methadone, meperidine, dextromethorphan, diphenoxylate (CU)
Pain, cough suppression (dexatromethorphan), diarrhea (loperamide and diphenoxylate), acute pulmonary edema, maintenance programs for heroin addicts (methadone)
Morphine, fentanyl, codine, loperamide, methadone, meperidine, dextromethorphan, diphenoxylate (T)
Addiction, respiratory depression, constipation, miosis, additive CNS depression with other drugs. Tolerance does not develop to miosis and constipation. Toxicity treated with naloxone and naltrexone (opioid receptor antagonist)
Butorphanol (MOA)
Mu-opiod receptor partial agonist and kappa-opiod agonist; produces analgesia
Butorphanol (CU)
severe pain (migraine, labor). causes less respiratory depression than full opioid agonist.
Tramadol (MOA)
Very weak opioid agonist; also inhibits serotonin and norepinephrine reuptake (works on multiple neurotransmitters- “tram it all”)
Tramadol (CU)
Chronic pain
Tramadol (T)
similar to opioids. decreases seizure threshold. serotonin syndrome.
Ethosuximide (MOA)
Blocks thlamic T-type Ca channels
Ethosuximide (CU)
Generalized absence seizures
Ethosuximide (T)
EFGHIJ; Ethosuximide causes Fatigue, GI distress, HA, Itching, stevens-Johnson syndrome
Benzodiazepines (Diazepam, Lorazepam) (MOA)
increases GABA action
Benzodiazepines (Diazepam, Lorazepam) (CU)
Status epilepticus
Benzodiazepines (Diazepam, Lorazepam) (T)
Sedation, tolerance, dependence, respiratory depression
Phenytoin (MOA)
increases Na channel inactivation; 0 order kinetics
Phenytoin (CU)
Status epilepticus and tonic-clonic seizures
Phenytoin (T)
Nystagmus, diplopia, ataxia, sedation, gingival hyperplasia, hirsutism, peripheral neuropathy, megaloblastic anemia, teratogenesis (fetal hydantoin syndrome), SLE like syndrome, induction of cytochrome P-450, lymphadenopathy, Stevens-Johnson syndrome, osteopenia
Carbamazepine (MOA)
increases Na channel inactivation
Carbamazepine (CU)
Drug of choice for Complex partial seizures, also used for tonic-clonic seizures
Carbamazepine (T)
Diplopia, ataxia, blood dyscrasias (agranulocytosis, aplastic anemia), liver toxicity, teratogenesis, induction of cyp P450, SIADH, Steven-Johnson syndrome
Valproic acid (MOA)
Increases Na channel inactivation, increases GABA concentration by inhibiting GABA transaminase
Valproic acid (CU)
Drug of choice for pts with tonic-clonic and absence seizures