Pharm Quiz Flashcards

USA MCN568 FALL2019 (41 cards)

1
Q

Pharmacokinetics

A

how drug enter and exits the body, what YOU do to the DRUG

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2
Q

Pharmacokinetics steps

A

absorption, distribution, metabolism, excretion

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3
Q

absorbtion

A

drug transfer from site of administration to blood stream

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4
Q

distribution

A

central circulation to peripheral tissue

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5
Q

metabolism

A

bio-transformation: converting molecules

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6
Q

excretion

A

removal

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7
Q

pH changes and drug absorption

A
low pH (acid) increases absorption of weak acids (furosemide, phenobarbital)
high pH  (base) increases absorption of weak based, and decrease absorption of weak acid
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8
Q

neonate distribution

A

body composition: water( 70-75% and fat 15-28% term; protein binding: low albumin concentration, less binding

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9
Q

neonate metabolism

A

liver- deficiency in enzymes

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10
Q

PHASE I liver metabolism

A

P450, oxidation, reduction, hydrolysis

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11
Q

PHASE II liver metabolism

A

conjugation w/sulfate, acetate and glucoronic acid

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12
Q

neonate excretion

A

kidneys GFR tubular secretion and re-absorption

neonate has: larger volume of distribution, delay excretion, need higher mg/kg dose, longer dosing intervals

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13
Q

bioavailibility

A

fraction of the administered drug that reaches circulation; IV 100%

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14
Q

half life

A

is the time it takes for half of the drug to clear the plasma or the time it takes to reduce concentration in half

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15
Q

steady state

A

concentration of the drug in the maternal circulation that determines the amount of drug available to the fetal compartment; rate of drug administration equals rate of excretion

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16
Q

loading dose

A

long half life…long time to achieve plateau…larger initial dose

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17
Q

placental transfer of drugs

A

increase in maternal far, decrease in serum protein, changes in P450 and UGT; placental changes (surface and thickness);

18
Q

teratogenic

A

anything external to fetus that causes structural or functional disability in prenatal or postnatal life

19
Q

pregnancy risk categories DRUGS

A

A-safe
B-animal safe, no human data
C-animal adverse effect; no human date; benefits outweigh the risk
D human risk; potential benefit outweigh risk
X fetal abnormalities, risk> benefits

20
Q

AGONIST

A

activator of the receptor; stimulates response; has affinity and intrinsic activity

21
Q

ANTAGONIST

A

inhibitor of receptor, blocks agonist, block response; has affinity but no intrinsic activity

22
Q

METABOLISM

A

the rate of drug metabolism is the
primary determinant of both duration and
intensity of drug action

23
Q

Pharmacodynamics

A

What DRUGs do to YOU

  • Receptors and mechanisms of action
  • Stimulators (agonists)
  • Blockers (antagonists)
  • Dose-response relationships
  • Therapeutic effects versus toxic effects
24
Q

example of teratogenic drugs

A

thalidomide, valproic acid, carbamazepine, ACE inhibitor, ARBs, tetrecycline, paroxetine, AEDs

25
neonatal gastric acid production
low at birth few hours of life pH 1-3 first 10 days of life...near neutral premature: pH 6-8 first 14 days of life
26
drug specific factors DISTRIBUTION
molecular size, ionization constant, relative hydrophilic/lipophilic properties; protein bounding
27
infant specific factors DISTRIBUTION
body composition, membrane/tissue permeability; cardiac output
28
volume of distribution
Vd: hypothetical fluid volume through which the drug is dispersed
29
NEONATE Vd
Vd is high/large, lowering max drug concentration, drug clearance is slow...need higher dose
30
delay drug clearance causes?
prolonged half-life
31
FAS
greatest single drug-induced cumulative preventable intellectual deficit in children
32
NAS opioids
clinical presentation: CNS and GI S&S
33
intubation meds
fentanyl 1-3ug/kg or midazolam 0.1mg/kg
34
circumcision meds
PO sucrose, acetaminophen, lidocaine block
35
chest drain meds
fentanyl, local anesthetic, non-pharm measures
36
ophthalmology exam meds
anesthetic drops, sucrose, containment
37
post op
police and around the clock, preventative, morphine, fentanyl, acetaminophen
38
therapeutic drug monitoring
appropriate dosing, modification for desired drug concentrations (t) tau interval, (n) number of doses
39
peak level
30 minutes post end of infusion
40
trough level
60 minutes prior next dose administration
41
NEO meds requiring monitoring
gentamicin, vancomicin, phenobarbital