Pharm final- old stuff Flashcards

1
Q

What is the MOA of phenytoin?

A

-selective inhibition of sodium channels
-slows recovery of Na channels from the inactive state

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2
Q

What are some ADRs r/t phenytoin?

A

-SJS/ toxic epidermal necrolysis> associated with genetic mutation
-gingival hypertrophy
-hyperplasia>excessive growth of gum tisue
-reduced with folic acid
- regularly brush teeth, floss gently
-interferes with metabolism of vitamin D (Do not give to an older adult who already has osteoporosis)
-hirsutism

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3
Q

What are some ADRs r/t phenytoin?

A

-SJS/ toxic epidermal necrolysis> associated with genetic mutation
-gingival hypertrophy
-hyperplasia>excessive growth of gum tissue
-reduced with folic acid
- regularly brush teeth, floss gently
-interferes with metabolism of vitamin D
-hirsutism

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4
Q

MOA of valproic acid?

A
  • suppresses neuronal firing by blocking sodium channels
    -suppresses calcium influx by blocking calcium channels
    -potentiates the inhibitory influence of GABA
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5
Q

What is a drug interaction of valproic acid?

A

-topiramate (hyperammonemia)
-excessive ammonia in body when these drugs are combined

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6
Q

How may a patient appear if valproic acid and topiramate are combined?

A

-confusion
-vomiting
- altered LOC

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7
Q

What is the drug of choice for absence seizures?

A

Ethosuximide

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8
Q

What are some ADRs of lamotrigine?

A

-life-threatening rashes (SJS and TEN)
-Aseptic meningitis
(confusion, photophobia, n/v, Nuchal rigity (main sign), inflammation of the meninges)

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9
Q

What is the MOA of vigabatrin?

A

-inhibits GABA transaminase
- Prevents GABA inactivation, so it enhances GABA mediated inhibition of neuronal activity

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10
Q

What is the MOA of Ezogabin?

A

Promotes potassium efflux in the neuronal membrane
(nonselective)
It activates potassium channels in the bladder which can cause urinary retention

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11
Q

What are some therapeutic uses of Gabapentin?

A

-Neuropathic pain
-migraine prophylaxis
-fibromyalgia
-Postmenopausal hot flashes

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12
Q

Endogenous opioids work on..

A

Mu, Kappa, delta

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13
Q

Exogenous opioids work on…

A

MU and Kappa

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14
Q

Mu side effects include?

A

-respiratory depression
-euphoria

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15
Q

Kappa side effects include?

A
  • no euphoric effects
    -decreased potential for addiction
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16
Q

What is the prototype for a pure opioid agonist? (STRONG)

A

Morphine
-activates Mu and Kappa receptors
-most effective against constant, dull pain

17
Q

Prototype for moderately strong opioid agonist?

A

Codeine
-used to control mild/moderate pain

18
Q

What is the prototype for agonist-antagonist opioid (partial agonist)

A

Pentazocine
-no euphoric effects
-less abuse potential

19
Q

Pentazocine acts as an _____ at kappa receptors and an _______ at Mu receptors.

A

agonist
antagonist

20
Q

What is the prototype for a pure opioid antagonist?

A

Naloxone
-used to diagnose and treat overdose

21
Q

What are some adverse effects of morphine?

A

-Resp. depression
-orthostatic hypotension
-Neurologic effects (sedation, euphoria, elevation of ICP, miosis)
-Cough suppression
-constipation
-Promotes N/V/ emesis
-Urinary retention

22
Q

How do you monitor the effectiveness of furosemide?

A

-daily weight, urine output ( OUTPUT SHOULD EXCEED INTAKE), decreased edema, clear lung sounds

23
Q

What are some ADRs of furosemide?

A

-hypovolemia, hypokalmeia, hypochloremia, hyponatremia
-hyperglycemia, hyperuricemia, high LDL, high triglycerides
-ototoxicity
-hypotension
-Arrythmias (low potassium)
-metabolic alkalosis

24
Q

What are some drug interactions with furosemide?

A

-Antihypertensives- lowers BP
-Digoxin- Toxicity
-Aminoglycosides- ototoxicity
-Lithium- low sodium level
-NSAIDS
-Potassium-sparing diuretics (POSITIVE)

25
Q

What can you teach your patient that is taking furosemide?

A

-They will pee ALOT
-stand up slowly
-increase potassium intake for potassium eliminating diuretics
- take in the morning if QDAY and morning afternoon if BID
-hypokalemia s/s= muscle weakness
- Call provider if they gain more than 2 llbs in a day, experiencing SOB, changes in hearing, or pain in joints= GOUT

26
Q

What is the difference between ADRs of hydrochlorothiazide compared to furosemide?

A

Same ADRs as furosemide EXCEPT ototoxicity and hypocalcemia

27
Q

What are some advantages of using hydrochlorothiazide compared to furosemide?

A

-Protects against post-menopausal osteoporosis
-prevents calcium-induced renal calculi
-Enhances actions of ADH- can be used for diabetes insipidus

28
Q

MOA of spironolactone?

A
  • Acts at late distal tubule to decrease both sodium reabsorption and potassium secretion
29
Q

What are some ADRs of spironolactone?

A

-Androgenic effects
-impotence
-hirsutism
-gynecomastia/amenorrhea