Adverse Drug Effects & Toxicology Flashcards

(39 cards)

1
Q

What is a graded dose response curve?

A

Measures response of increased dose given to an individual on a continuous scale

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2
Q

What is a quantal response curve?

A

Characterize all-or-nothing pharmacologic response

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3
Q

What are the midpoints that the therapeutic index compares?

A

Midpoints: ED50 and LD50

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4
Q

Therapeutic index = ?

A

TI=LD50/ED50

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5
Q

What does the therapeutic index measure?

A

Factor, by which the effective dose for 50% of the population must be increased to cause negative side effect in 50% of the population

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6
Q

Does a high therapeutic index correlated with a more dangerous or safe drugs?

A

Safe

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7
Q

What does the standard safety margin compare?

A

Extremes ED99 and LD1

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8
Q

SSM = ?

A

[(LD1/ED99)-1]*100

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9
Q

What does the standard safety margin measure?

A

The percent by which effective dose in 99% of the population must be increased to cause negative side effect in 1% of the population

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10
Q

What are extension effects?

A

Arise from therapeutic effect, they are dose related and predictable

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11
Q

What are side effects?

A

Unrelated to the therapeutic goal, they are predictable and dose dependent

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12
Q

What is the difference between adverse drug reactions and toxic reactions?

A

Adverse drug reactions occur at usual therapeutic doses, toxic reactions occur outside therapeutic range

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13
Q

What is an idiosyncratic reaction?

A

Genetically determined, abnormal and unpredictable response to drug

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14
Q

What are the possible pharmacologic consequences of drug drug interactions?

A

Enhancement or antagonism of drug via the same target

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15
Q

What are the possible physiologic consequences of drug drug interactions?

A

Enhancement or antagonism of drug via distinct effector system

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16
Q

What patients are at high risk for drug drug interactions?

A

Elderly, high risk clinical situations, renal/hepatic disease, multiple prescribing physicians

17
Q

Drug drug interactions may influence gastric motility. If there is a decrease in motility by drug B, what is the effect on drug A?

A

Drug A will have a lower peak plasma concentration and decreased absorption rate

18
Q

If drug B is given after drug A and changes the pH so that drug A can not be absorbed, what is the effect on the bioavailability of drug A.

A

Reduced bioavailability

19
Q

Drug B is given after Drug A. Drug B decreases cardiac output. What is the effect on Drug A?

A

Increased plasma levels due to decreased hepatic clearance

20
Q

Clinically, what is the most significant consequence of drug-drug interactions?

A

Changes in metabolic processing of drug (inducers/inhibitors)

21
Q

Does Rifampin induce or inhibit drug metabolism?

22
Q

Do erythromycin and azole antifungals induce or inhibit drug metabolism?

23
Q

Is phenobarbital an inducer or inhibitor of drug metabolism?

A

Phenobarbital

24
Q

What is the single most important determinant of poising outcomes?

A

Provision of good supportive care

25
What are the general pharmacokinetic treatment strategies for toxins?
Decrease absorption, increase elimination
26
What are pharmacodynamic strategies for toxins?
Antidote, limited
27
What is syrup of ipecac?
Induces emesis to empty stomach contents
28
What percent of poisons are removed by emesis plus gastric lavage?
30%
29
What is the mechanism of action for charcoal?
Binds drug in gut to limit absorption
30
What are osmotic cathartics?
Laxatives
31
When would you want to avoid giving a patient magnesium citrate or sulfate?
If they have renal disease, or toxin is nephrotoxic
32
When would you want to avoid giving a patient sodium sulfate?
CHF or hypertension
33
What type of drug is polyethlene glycol?
Osmotic cathartics
34
When do methanol and ethylene glycol become toxic?
After they undergo metabolism to formic acid and oxalic acid respectively
35
What is the rate limiting enzyme that metabolizes methanol and ethylene glycol?
Alcohol dehydrogenase
36
What drugs can inhibit alcohol dehydrogenase?
Fomepizole, ethanol
37
Most acetaminophen is safely eliminated. What percent becomes a hepatotoxic metabolite?
10% becomes NAPQI
38
What drug is given to enhance NAPQI detoxification?
N-acetylcystein
39
When is hemoperfusion used to enhance elimination of a toxin?
High molecular weight toxins with poor water solubility