Drug Monitoring Flashcards

1
Q

Advantages

A

-Nonadherence can be identified
-Variations in drug-disposition patterns
-Altered drug utilization
-Compensation for an altered state
-Drug interactions

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2
Q

Phenytoin

A

Exhibits saturated kinetics so TDM necessary

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3
Q

Theophylline

A

-PK is age dependent
-Phenytoin and phenobarbital increase theophylline clearance 2 fold
-OD tx with charcoal and hemodialysis

CHAPP

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4
Q

Valproic Acid (depa)

A

-Increases GABA
-Half life varies with age, duration, liver function
-Rapid and complete absorption

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5
Q

Phenobarbital

A

-Hyperpolarizes GABA(A) receptor
-Slow and complete absorption

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6
Q

Primidone

A

-Phenobarbital contributes to effect
-Rapid and complete absorption
-Phenobarbital is active metabolite and the dose is titrated to obtain therapeutic conc of phenobarbital

CPR

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7
Q

Carbamazepine

A

-Slow and erratic absorption
-Carb-10-11-epox accumulates in children
-Highly protein bound

SPEC

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8
Q

Ethosuximide

A

-Readily absorbed from GI tract

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9
Q

Digoxin

A

-Variably absorbed
-25% protein bound
-Serum drawn as a trough (8 hr post dose)

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10
Q

Procainamide

A

-Fast acetylators form more NAPA which accumulates in plasma
-NAPA also accumulates in RF

NAPA in FARF

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11
Q

Aminoglycosides

A

-Poorly abs orally
-Peak for therapeutic response, trough for toxicity

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12
Q

Cyclosporine

A

-Highly variable abs
-Whole blood conc correlates well with IS/tox

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13
Q

Vancomycin

A

-Trough 10-20
-AUC 400-600
-90% renal exc

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14
Q

Sirolimus

A

-AE: pneumocystis carinii infection
-Excreted in feces
-Combo with cyclosporine and CS

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15
Q

Tacrolimus

A

-Excreted in feces
-Should NOT be used with cyclosporine

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16
Q

Draw trough immediately prior to next dose

A

-IM, peak at 45-60 min post dose
-30 min IV, peak at 30 min post dose
-60 min IV, peak 15 min post dose