Pharm Basics Flashcards

1
Q

What is pharmacokinetics?

A

What our body does to the drug

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2
Q

What is pharmacodynamics?

A

How the drug affects our body

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3
Q

What is the difference between therapeutic and pharmacologic drug classifications?

A

Therapeutic: usefulness in treatment; how the drug treats
Pharmacologic: physiological effect on molecular/tissue level; how the drug works

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4
Q

Difference between chemical, generic, and brand/trade names of drugs.

A

Chemical: structure
Generic: name of actual medication (important for tests/NCLEX)
Brand: name given to drug by the pharmaceutical company

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5
Q

Process in which drugs are developed and come to market.

A

Preclinical phase: tested on lab animals
Phase I: tested on healthy human volunteers
Phase II: tested on clients with disease
Phase III: large sample size approved by FDA
Phase IV: usually 2+ years post market, new or adverse affects — recall

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6
Q

What are the responsibilities of the Food and Drug Administration (FDA)?

A

Protects public health by ensuring safety, efficiency, and security of drugs, biological products & medical devices.
— Also includes safety of food supply, cosmetics & products that emit radiation

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7
Q

Function of the DEA (Drug Enforcement Agency)

A

Regulates manufacturing, distribution, and dispensing of drugs with known abuse potential (controlled substances).
*Nurses must be familiar with regulations and standard of practice.

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8
Q

Schedule I drugs:

A

— high abuse potential
— not for medical use
Ex: heroin

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9
Q

Schedule II drugs:

A

— high abuse potential
Ex: narcotics

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10
Q

Schedule III drugs:

A

— moderate
— less abuse
Ex: sedatives

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11
Q

Schedule IV drugs:

A

— moderate
— less abuse
Ex: anxiety agents

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12
Q

Schedule V drugs:

A

— limited abuse
Ex: codeine

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13
Q

What is a teratogenic drug?

A

Drugs that can cause birth defects
— cross placental barrier

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14
Q

Primary adverse effect:

A

Overdose; extension of desired effect

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15
Q

Secondary adverse affect

A

Undesired effect, must be tolerated
— undesired effect produced in addition to pharmacologic effect

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16
Q

How does toxicity effect the liver?

A

Fever, nausea, jaundice

17
Q

How does toxicity affect the kidneys?

A

— oliguria
— increased BUN
— increased creatinine

18
Q

How does toxicity effect the nervous system?

A

Change in LOC, cognition & behavior

19
Q

What is happening to the body during an allergic reaction?

A

Anaphylaxis: bronchoconstriction, response to histamine
— delayed allergic reactions can also occur

20
Q

What are contradictions in drug therapy?

A

Example: having a bleeding disorder is a contradiction for taking aspirin due to excess bleeding

21
Q

Drug-food interactions:

A

— acid production: speeds breakdown of drug
— milk products: calcium binds to drug, decreases absorption
— chemical reaction: iron binds with tetracycline
— liver enzymes: grapefruit juice (48hr after ingesting), enzyme inhibitor: toxic drug effects

22
Q

What are the 6 rights of medication administration

A

Right:
Drug, dose, route, time, patient, documentation

23
Q

What are the four phases of pharmacokinetics?

A
  1. Absorption: drug to blood
  2. Distribution: drug to tissue
  3. Metabolism: breaking drug down
  4. Excretion: getting drug out of body
24
Q

What are factors that alter absorption of an oral drug?

A

— composition of drug is too big, cannot pass thru membrane
— highly lipid soluble drugs: dissolve before absorbed correctly
— foods and fluids (binding)
— multiple drugs (interaction)
— enteric coating tablets

25
Q

What factors alter drug distribution?

A

— blood flow to tissue
— ability to cross blood-brain barrier
— protein binding: albumin; molecule gets too big
— water-soluble: stays in blood stream
— lipid-soluble: rapidly passes membrane and deposits into adipose tissue

26
Q

Explain the “first pass effect”

A

Oral drug—absorbed across intestinal mucosa—enters portal circulation, travels to liver—drug is metabolized to less active form—leaves liver to distribute to tissues
*less active

27
Q

What is the liver’s role in metabolism of drugs?

A

— transforms drug into active form
— breakdown drug for excretion
— hepatic microsomal enzyme system
— metabolism

28
Q

What organs are primarily involved with excretion of drug byproducts?

A

Kidneys

29
Q

Explain therapeutic response

A

Response after treatment of any kind, usually a useful and favorable response

30
Q

What is onset, peak, and duration of drugs?

A

Onset: time for drug to elicit a therapeutic response
Peak: time for drug to reach maximum therapeutic response
Duration: time of drug concentration sufficient to therapeutic response

31
Q

What is an agonist?

A

Causes the same activity of a natural chemical
Ex: insulin, beta-agonist

32
Q

What is an antagonist?

A

Blocks normal stimulation of receptor
Ex: beta-blockers, anti-histamines

33
Q

What is peak and trough?

A

Trough: lowest drug level needed to reach therapeutic range; lowest level of drug in bloodstream
— drawn 1hr prior to start of next medication
Peak: highest level of drug in bloodstream
— drawn 1hr after infusion is completed

34
Q

What information should be included in patient education?

A

— name of drug
— dosing
— action
— timing
— storage and prep
— measuring
— what to avoid
— monitoring symptoms and vitals
— adverse effects
— toxicity
— warnings
— special considerations
*verify patient understanding

35
Q

What is the difference between medication error and adverse effect?

A

Adverse drug effect: side effect; anticipated or unanticipated
Medication error: error in process that leads to adverse effect
— ex: higher than acceptable dose given; drug-drug interaction

36
Q

What are the functions of the sympathetic nervous system?

A

— “fight or flight”
— decreased urination (retention)
— decreased digestion
— increased feelings of stress, anxiety, & danger
— system’s activity increases

37
Q

What receptors are involved in the sympathetic nervous system?

A

Adrenergic AGONIST: sympathomimetic; used for cardiac + respiratory
— tachycardia
— vasoconstriction
— bronchodilation
— decreased GI activity
— glycogenolysis (increased blood glucose)
— constricts bladder sphincter
Adrenergic ANTAGONIST: blocking normal action; Adrenergic blocking, alpha-beta blocker; used for HTN
— slows HR
— decreases BP
— bronchoconstriction
— hypoglycemia
— urinary incontinence

38
Q

What are the functions of the parasympathetic nervous system?

A

— “rest and digest”
— decreases HR
— constricts bronchioles
— increases digestions
— increases urination

39
Q

What receptors are involved with the parasympathetic nervous system?

A

Cholinerigic AGONIST: mimics acetylcholine; used for Alzheimer’s
— increased saliva production
— deceased HR
— constricts bronchioles
— increases digestion
— increased urination
ANTAGONIST: anti-cholinergic; cholinergic blocking; used for bowel & bladder disease, Parkinson’s, and asthma
— decreased saliva
— increased HR
— relaxes bronchioles
— slows digestion
— decreased urination