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91 Cards in this Set
- Front
- Back
Alpha agonists treating Glaucoma:
|
- Epinephrine
- Brimonidine |
|
What are side effects of epinephrine?
|
- mydriasis
- stinging |
|
Beta blockers treating glaucoma:
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- timolol
- betaxolol - carteolol |
|
Which diuretic treats glaucoma?
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- Acetazolamide (decreae HCO3)
|
|
What cholinomimetics treat glaucoma?
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- Direct: pilocarpine, carbachol
- Indirect: physostigmine, echothiophate |
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What are side effects of cholinomimetics?
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-miosis
- cyclospasm |
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How does cholinomimetics relieve glaucoma?
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- increase outflow of aqueous humor
- contract ciliary muscle and open trabecular meshwork |
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What prostaglandin is used for glaucoma?
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Latanoprost
|
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What is side effect of latanoprost?
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darkens color of iris (browning)
|
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How do you know if someone has closed angle glaucoma?
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- intense pain
- halos around lights |
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Which drugs are used for closed angle glaucoma?
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- pilocarpine
- acetazolamine - mannitol *rapid acting |
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What are opioid analgesics?
|
- morphine
- fentanyl - codeine - heroin - methadone - meperidine - dextromethorphan |
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Where are opioid receptors?
|
mu= morphine
delta= enkephalin kappa= dynorphin |
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Opioid
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MOA: open Ka+ channels; close Ca+ channels
Inhibit release of Ach, NE, 5HT, glutamate, substance P Use: pain, cough suppression, diarrhea, pulm edema, |
|
What is toxicity of opioid?
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- addiction
- resp depression - constipation - pinpoint pupils |
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Treat cough suppression:
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dextromethorpahn
|
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Treat dirrhea:
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- loperamide
- diphenoxylate |
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Meperidine + MAOI=
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serotonin syndrome
|
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Butorphanol:
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MOA: parital agonist at mu receptor and kappa receptor
Use: pain--> less respiratory depression |
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Heroin detox treatment:
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butorphanol
|
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Tramadol:
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MOA: weak opioid agonist
* inhibit Serotonin and NE reuptake "TRAM IT ALL" Use: pain |
|
Tramadol toxicity?
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decreases seizure threshold
|
|
1st line for Tonic-clonic seizure:
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- phenytoin
- carbamazepine - valproid acid (CVP) |
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1st line for Absence Seizure:
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- eposuximide
|
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1st line for Status epilepticus:
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- phenytoin
- Benzodiazepine |
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Which drugs ahve NO partial seizure activity?
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- ethosuximide
- benzodiazepine |
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Phenytoin
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increase Na+ channel inactivation
|
|
Carbamazepine:
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Increase Na+ channel inactivation
|
|
Lamotrigine :
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blocks voltage-gated Na+ channels
|
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Gabapentin:
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designed as GABA analog
* inhibit HVA calcium channels |
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Topiramate:
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block Na+ channel
* increase GABA |
|
Phenobarbital
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increase GABAa
|
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Valproic acid
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increase Na+ channel inactivation
* GABA increase |
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Ethosuximide
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Blocks T-type thalamic Ca+ channels
|
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Benzodiazepine
|
increase GABAa
|
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Tiagabine
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Inhibits GABA reuptake
|
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Vigabatirin
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Irreversibly inhibit GABA transaminase-- Increase GABA
|
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1st line for trigeminal neuralgia:
|
carbamazepine
|
|
Gabapentin is also used for:
|
- peripheral neuropathy
- bipolar |
|
1st line epilepsy drug for pregnant woman and child:
|
Phenobarbital
P for Pregnancy OKAY |
|
Valproic acid is used for _____ seizures also
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myoclonic
|
|
Treatment for eclampsia seizures:
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Benzodiazepine
|
|
1st line to prevent seizure of eclampsia:
|
MgSO4
|
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Benzodiazepine toxicity:
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- sedation
- tolerance - dependence |
|
Carbamazepine toxicity:
|
- diplopia
- ataxia - blood dyscrasias - agranulocytosis - aplastic anemia - liver toxicity - teratogenesis - induce p-450 - SIADH - Stevens Johnson |
|
Ethosuximide toxicity
|
- GI distress
- Fatigue - headache - urticaria - Steven Johnson Syndrome |
|
Phenobarbital
|
- sedation
- tolerance - dependence - induce P450 |
|
Valproic Acid
|
- GI distress
- fatal HEPATOTOXICITY (measure LFT) - Neural tube defect in fetus (spina bifida) - weight gain ** Dont give to pregnancy |
|
Lamotrigine
|
Stevens Johnson Syndrome
|
|
Gabapentine
|
Sedation
Ataxia |
|
Topiramate toxicity
|
sedation
kidney stones |
|
Ethosuximide toxicity pneumonic:
|
EFGH:
Ethosuximide Fatigue GI Headache |
|
What causes Stevens JOhnson syndrome?
|
- Carbamazepine
- Ethosuximide Lamotrigine CEL |
|
Phenytoin toxicity
|
- nystagmus
- diplopia - ataxia -sedation - gingival hyperplasia - hirsutism - megaloblastic anemia - teratogenesis - SLE like syndrome |
|
Phenytoin:
|
MOA: block NA+ channel
* Increase refractory period * inhibit glutamate release from excitatory presynaptic neuron Use: TOnic-clonic seizures; class IB |
|
Barbiturate:
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MOA: faciliatate GABAa by increase duration of Cl- channel opening
USE: sedative for anxiety, seizures, insomnia, induction of anesthesia Toxic: additive CNS depression with alcohol |
|
Barbituate is contraindicated in:
|
Porphyria
|
|
Benzodiazepine:
|
MOA: Facilitate GABAa by increase frequency of Cl- channel opening
* decrease REM sleep Use: anxiety; spasticity; status epilepticus; detox (DT); night terror; sleep walking; hypnotic Toxic: additive CNS depression with alcohol |
|
Treat benzo overdose with:
|
Flumazenil
|
|
Short acting Benzo:
|
TOM
Triazolam Oxazepam Midazolam |
|
Anesthestics are:
|
lipid soluble to cross BBB
|
|
For Rapid, high potent drug:
|
Low solublility in blood
High solubility in lipid |
|
Inhaled anesthetics:
|
- halothane
- enflurane - NO USE: myocardial depression, respiratory depression, nausea, increased cerebral blood flow |
|
Toxicity of inhaled anesthetics
|
hepatotoxicity (halothane)
nephrotoxicity (methoxyflurane) proconvulsant (enflurane) Malignant hyperthermia |
|
IV anesthetics
|
B.B. King on Opiates Proposes Foolishly:
Barbituate Benzo Ketamine Opiate Propofol |
|
Barbituate (Thiopental)
|
high potent
highl lipid *DECREASE CEREBRAL BLOOD FLOW |
|
Benzodiazepine
|
side effect: post-op respiratory depression; decreased BP; amnesia
|
|
Ketamine
|
PCP analog
* block NMDA receptors * INCREASE CEREBRAL BLOOD FLOW |
|
Propofol
|
potentiate GABAa
|
|
Local Anesthetics
|
- Ester (procaine, cocaine, tetracaine)
- Amides (lidocaine, mepivacaine, bupivacaine) 2 I's |
|
NM blockers
|
muscle paralysis
*Depolarizing: Succinylcholine * Non-depolarizing: -curarine |
|
Side effect of succinylcholine:
|
- hypercalcemia
- hyperkalemia |
|
Reversal of block of Succinylcholine:
|
phase i: no antidote (block potentiated by cholinesterase inhibitors)
phase ii: antidoe |
|
Dantrolene
|
- treat malignant hyperthermia
- treat NMS MOA: prevent Ca+ release from SR of skeletal muscle |
|
Parkinson:
|
high cholinergic
low dopamine |
|
Parkinson Drugs:
|
BALSA
Bromocriptine Amantadine Levodopa (carbidopa) Selegiline Antimuscarinics |
|
Bromocriptine:
|
agonize dopamine receptor
|
|
Amantadine
|
increase dopamine
(also antiviral vs influenza A and rubella) |
|
selegiline:
|
MAO-I B
* prevent dopamine breakdown |
|
Benztropine (antimuscarinic):
|
curb excess cholinergic activity
|
|
L-dopa/carbidopa is unlike dopamine because:
|
- crosses BBB and converted to dopa decarboxylase in CNS to dopamine
|
|
Carbidopa
|
peipheral decarboxylase inhibitor
|
|
Selegiline preferentially metabolizes:
|
Dopamine over NE and 5HT
|
|
What are alzheimer drugs:
|
- memantine
- donepezil; galantamine; rivastigmine |
|
Memantine:
|
NMDA receptor antagonist
* prevent excitotoxicity |
|
Donepezil; glantamine;rivastigmine
|
ACHe inhibitors
|
|
Huntington effect:
|
high dopamine
low GABA low ACh |
|
Huntington drugs:
|
- Reserpine + tetrabenazine
- Haloperidol |
|
Sumatriptan:
|
5HT 1b/1d agonist
USE: acute migraine, cluster headache TOXIC: coronary vasospasm "SUMo wrestler TRIPS AND falls on your head" |
|
Sumatriptan is contraindicated in:
|
= CAD
= Prinzmetal angina |
|
riluzole
|
NMDA receptor antagonist
* treat ALS |