ADME 3 Flashcards

1
Q

What are dose dependent ADRs of phenytoin?

A
Nystagmus
Vertigo 
Diplopia 
Ataxia 
Drowsiness 
Speech disturbances
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Does unbound phenytoin increase in renal failure?

A

Yes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How would you describe phenytoin metabolism?

A

Non linear and zero order pharmacokinetics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the method commonly used to measure phenytoin concs?

A

CEDIA cloned enzyme donor immunoassay

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

When should digoxin serum levels be monitored?

A

IV - 4 hours after

Or 6 hours after oral

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the methods used to monitor serum digoxin concs?

A

Radioimmunoassay
Fluorescence polarisation immunoassay
Enzyme immunoassay

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

When should digoxin be measured?

A

Borderline renal function
Aged subjects
Patients with AF who require higher digitalis doses for HR control
Heart failure patients

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Which drugs don’t need monitoring?

A

Drugs used in diseases with clear clinical end points
When serum concs don’t correlate with therapeutic of toxic effects
Straightforward pharmacokinetics
Drugs used in non life threatening diseases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Do drug metabolites clear more quickly than parent drug?

A

Yes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What scenarios are important when monitoring phenytoin?

A

Establishing an individual therapeutic conc
Aiding in diagnosis of clinical toxicity
Dosage adjustment to patients with greater pharmacokinetic variability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly