1 - Errors, Reactions, Special Populations Flashcards

1
Q

What is a side effect?

A

A nearly unavoidable secondary drug effect produced at therapeutic doses

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2
Q

What is the technical definition of toxicity?

A

A detrimental physiologic effect caused by a supratherapeutic drug dose

However, usually used to refer to any severe ADR, even if the dose that caused it was therapeutic

Severe neutropenia from chemo can be considered toxicity, even though it’s produced because the drug dose is therapeutic

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3
Q

What percent of adverse drug reactions are true allergies?

A

10%

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4
Q

The intensity of an allergic reaction is determined primarily by:

A

the degree of sensitization of the immune system

NOT the size of the dose

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5
Q

Most serious allergic reactions are caused by one drug family:

A

the penicillins

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6
Q

What is an idiosyncratic effect?

A

an uncommon drug response resulting from a genetic predisposition

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7
Q

Give an example of an idiosyncratic effect

A

When patients with G6PD take sulfonmamides or aspiring they develop hemolysis

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8
Q

What does iatrogenic mean?

A

Caused by medical care or treatment or drugs

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9
Q

What percentage of medication errors occur when patients undergo a transition in care?

A

60%! This is why med recs are so essential

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10
Q

How effect is BCMR?

A

Reduces error by 85%

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11
Q

What are the top four pathologic conditions that profoundly effect drug response?

A
  1. Kidney Disease
  2. Liver Disease
  3. Acid-Base Imbalance
  4. Altered Electrolyte Status
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12
Q

Kidney disease reduces ______

Liver disease reduces ______

A

excretion

metabolism

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13
Q

It actually is not very common for electrolytes to alter the effectiveness of a drug. What is a notable exception?

A

Digoxin

In the presence of hypokalemia, it is very likely to induce dysrhythmias

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14
Q

What is the difference between pharmacodynamic tolerance and metabolic tolerance?

A

Pharmaco: result of chronic receptor occupation, resulting in an increased MEC

Metabolic: tolerance that results from accelerated drug metabolism. Some drugs (like barbiturates) induce the synthesis of hepatic drug-metabolizing enzymes, so the more drug you take, the more metabolizing enzymes the body makes. Interestingly, does not effect the MEC. Only the duration.

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15
Q

What is tachyphylaxis?

A

reduction in drug responsiveness due to repeated dosing over a short period in time

(constant nitroglycerin - like a patch - results in a loss of cofactor. intermittent dosing, on the other hand, allows cofactor to build back up between doses and prevents tachyphylaxis)

(Also, pitocin for labor)

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16
Q

Enteric coatings, sustained release, and chewable tablets are examples of formulations that alter:

A

bioavailability

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17
Q

Bioavailability differences occur primarily with _____ preparations, not ______

A

oral

IV

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18
Q

For a drug that is absorbed in the intestines, how would you expect diarrhea to effect bioavailability?

Constipation?

A

Decrease, due to less time in the intestines

Increase, due to excessive time in the intestines

19
Q

What’s the difference between genetics and genomics?

A
  • Genetics*: how genetic traits are passed from one generation to another
  • Genomics*: study of the genome and how genes interact with each other and the environment
20
Q

What is pharmacogenomics?

A

The study of how genes affect a person’s response to drugs

21
Q

What is a biomarker?

A

A measurable substance that indicates the existence of a genetic variation

22
Q

Genetic variations usually alter drug response by altering:

A

metabolism

23
Q

What is a possible explanation for increased efficacy of beta blockers in caucasions?

A

European ancestry has higher incidents of variants in genes that code for B1 ADRs that make them hyper-sensitive to beta blockers

24
Q

How does pregnancy influence GFR?

A

By the third trimester, it’s doubled

results in accelerated clearance

25
Q

If a patient with seizures becomes pregnant, will their drug dose need to be changed?

A

If it’s phenytoin, carbamazepine, or valproic acid, it will

The hepatic clearance of these three drugs is increased during pregnancy

26
Q

Why is heparin avoided during pregnancy?

A

It causes osteoporosis and can cause compression fractures of the spine

27
Q

What percent of congenital anomalies are genetic?

A

25%

28
Q

If you don’t want a medication to be passed through breastmilk, when is the ideal time to take a dose?

A

Immediately after breastfeeding

29
Q

How long does it take for gastric acidity to reach normal levels in infants?

A

two years!

30
Q

How are IM injections absorbed in the neonate?

in the infant?

A

very slow and erratic

More rapid even than in adults

31
Q

How is transdermal absorption altered in infancy?

A

much more rapid and complete in infants than in older children and adults

32
Q

Is protein binding increased or decreased in infants?

A

Decreased.

Low albumin, and endogenous compounds (fatty acids, bilirubin) are competing with drugs for binding sites

33
Q

If you gave a protein bound drug to an adult and an infant, who would have the higher free levels?

A

The infant, which will intensify the effect

34
Q

When does protein-binding capacity reach adult values?

A

10-12 months

35
Q

At what age are adult levels of renal function acheived?

A

1 year

36
Q

Do children (>1 year) metabolize drugs faster or slower?

A

Faster

37
Q

How is absorption altered in geriatric patients?

A

The percentage of an oral dose that is absorbed does NOT change with age

The rate at which that does is absorbed DOES slow down

(d/t delayed gastric emptying and reduced splanchnic blood flow)

38
Q

What are the four major factors that alter drug distribution in older adults?

A
  1. Increased percentage of body fat (forms a lipid-soluble storage depot, which reduces plasma levels and reduces response)
  2. Decline in lean body mass and total body water (water soluble drugs are distributed very little, leading to very high serum values and more intense effects)
  3. Reduced concentration of albumin (causes free levels of drugs to rise)
39
Q

How is drug metabolism impacted in geriatric patients?

A

hepatic drug metabolism tends to decline

d/t reduced hepatic blood flow, reduced liver mass, decreased activity of some hepatic enzymes

40
Q

What is the most important cause of the high prevalence of adverse drug reactions in the geriatric population?

A

drug accumulation secondary to reduced renal excretion

41
Q

What is the proper lab test to determine renal function in older adults?

Why?

A

creatinine clearance, NOT serum creatinine

In older patients, their serum creatinine will be low simply because they have less muscle mass. As such, creatinine serum levels may be normal even though the kidneys are functioning very poorly

42
Q

Are beta blockers more or less effective in geriatric patients?

Why?

A

Less, even when present in the same concentration

May be due to a reduction in the number of beta receptors and/or a reduction in the affinity of the remaining beta receptors for the blocking agents

43
Q

ADRs are ______ more common in older adults

A

7x

44
Q

Which is a more common reason for hospital admissions due to nonadherence: underdosing or overdosing?

A

90% of the time its under dosing, leading to a therapeutic failure