AEM's and Triptans Flashcards

1
Q

carbamazepine

A
enhanced fast inactivation of Na channel
broad spectrum
CYP450 inducer, auto-induction (self metabolism)
Toxicities:
- Hematoogical penias
- hypocalcemia/vit. D. def/ osteoporisis
-hepatotoxicity
-hyponatremia
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2
Q

oxcarbazepine

A

enhanced fast inactivation of Na channel
fewer CNS/ hematological side effects
less potent CYP450 inducer compared to carbamazepine
Renal clearance instead of hepatic

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3
Q

eslicarbazepine

A

enhanced fast inactivation of Na channel

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4
Q

lamotrigine

A

enhanced fast inactivation of Na channel

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5
Q

phenytoin

A
enhanced fast inactivation of Na channel
broad spectrum
Zero order pharmkinetics (Saturable)
inducer of CYP450
Toxicities:
- gingival hyperplasia 
- hypothyroidism
- hypocalcemia/Vit.D def/osteoporosis
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6
Q

topiramate

A
enhanced fast inactivation of Na channel
AMPA receptor antagonist 
GABA agonist 
broad spectrum 
renal clearance
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7
Q

valproic acid

A

enhanced fast inactivation of Na channel
inhibition GABA metabolism by GABA-T or SSD
promotes GABA production via glutamic acid decarboxylase
T-type Ca channel antagonist for absence seizure
broad spectrum

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8
Q

zonisamide

A

enhanced fast inactivation of Na channel

T-type Ca channel antagonist for absence seizure

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9
Q

lacosamide

A

enhanced fast and slow inactivation of Na channel

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10
Q

perampanel

A

AMPA receptor antagonist

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11
Q

Felbamate

A

NMDA receptor antagonist at glycine site

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12
Q

Tiagabine

A

GABA reuptake inhibitor of GAT-1

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13
Q

Vigabatrin

A

inhibitor of GABA met. by GABA-T
Ocular toxicity w/ central retinal damage
renal clearance

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14
Q

barbiturates

A

phenobarbital (broad spectrum) and primidone(for tonic/clonic)
GABA independent
increase duration of Cl- channel opening

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15
Q

benzodiazapines

A

lorazepam, diazepam, clonaxepam (for myoclonic), clorazepate
potentiates GABA binding to receptor, allosteric change
increases chloride conductance
GABA dependent

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16
Q

ethosuximide

A

T-type Ca channel antagonist

used for Absence seizures only

17
Q

Levetiracetam

A

Synaptic vesicle protein

renal clearance

18
Q

Brivaracetam

A

synaptic vesicle protein

19
Q

Gabapentin

A

alpha-2-delta Ca channel

renal clearance

20
Q

pregabalin

A

alpha-2-delta Ca channel

renal clearance

21
Q

Status epilepticus drugs

A

lorazepam, diazepam, phenobarbital, phenytoin, valproic acid, levetiracetam

22
Q

phenobarbital

A

C-IV agent
CYP450 inducer
CNS depressant
hypocalcemia/Vit.D def./ osteoporosis

23
Q

CYP450 inducer interactions

A

carbamazepine, phenytoin, phenobarbital, valproate

  • increase clearance of contraceptives
  • increased clearance of warfarin
  • increased clearance of antivirals
24
Q

Inhibitors of glucruonosyltransferases (UGT)

A

valproic acid and lamotrigine

causes accumulation of parent drug

25
inducers of UGT
phenytoin, carbamazepine, phenobarbital | cause reduction of parent drug
26
Other triptans
``` almotriptan naratriptan zolmitriptan rizatriptan eletriptan frovatriptan ```
27
Naratriptan
70% bioavailability, half-life 6 hrs
28
Zolmitriptan
5HT1d agonist on synaptic terminal | fast onset nasal spay
29
frovatriptan
half-life 24 hrs
30
sumatriptan
fastest onset with SC or nasal spray | half-life 1-2 hrs
31
MOA inhibitors
sumatriptan, rizatriptan and zolmitriptan contraindicated
32
dihydroergotamine (DHE)
interact with alpha, dopamine and 5HT receptors longer lasting effects but don't work as fast as triptans side effects include: - emetic action and severe vasoconstriction
33
Treatment during pregnancy
all trimesters = acetaminophen + codeine 1 and 2 trimester = aspirin or ibuprofen Triptans used cautiously never use DHE
34
migrane prevention
propranolol, timolol (decreases cortical spreading depression, CSD) Tricyclic antidepressants: - amitriptyline, imipramine Anticonvulsants: - topirimate, valproate Ca channel blocker: - verapamil (First choice for prevention)