Pharmacokinetics and the Nursing Process Flashcards

1
Q

Pharmacokinetics

A
  • determining how much of administered dose gets to its site of action
  • four major pharmacokinetic processes include drug absorption, distribution, metabolism, and excretion
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2
Q

Pharmacodynamics

A
  • the impact a drug has on the body

- looks at drug receptor interaction, the patient’s functional state, and placebo effects

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3
Q

Pharmaceutical properties of drugs

A

the medicinal properties of a drug; how it can benefit the individual it is effecting by minimizing the harm done

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4
Q

Pharmacokinetics: Absorption

A
  • the movement of a drug from its site of administration into the blood
  • amt of absorption helps to determine how intense effects will be
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5
Q

Pharmacokinetics: Distribution

A
  • defined as the transport of a drug in the body fluids from the bloodstream to the various tissues of the body & ultimately the site of action
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6
Q

Pharmacokinetics: Metabolism

A
  • also known as biotransformation
  • defined as the enzymatic alteration of drug structute
  • the process of chemically inactivating a drug by converting it into a more water-soluble compound or metabolite that can be excreted from the body
  • occurs in the liver
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7
Q

Pharmacokinetics: Excretion

A
  • the process by which drugs & metabolites are eliminated from the body, primarily through the kidneys
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8
Q

Blood Brain Barrier

A
  • only drugs that are lipid soluble or have a transport system have the ability to cross over the blood brain barrier to a significant degree and effect the CNS
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9
Q

Placental Drug Transfer

A
  • membranes of the placenta do not constitute an absolute barrier to the passage of drugs
  • movement across occurs from circulation, active transport, and even by passing directly through if they are lipid soluble
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10
Q

The Stages of Drug Research

A
  • preclinical testing

- clinical testing which includes 4 phases

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11
Q

Phase I clinical testing of drugs

A
  • initial pharmacologic evaluation

- small group of normal humans is tested to observe pharmacokinetics

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12
Q

Phase II clinical testing of drugs

A
  • limited controlled evaluation

- selected group of humans with targeted disease is tested. Subjects are monitored for effectiveness & side effects

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13
Q

Phase III clinical testing of drugs

A
  • extended clinical evaluation
  • humans with targeted disease are tested to determine clinical effectiveness, drug safety, estimated dosage range or tolerated dosage
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14
Q

Phase IV clinical testing of drugs

A
  • drug has been approved by the FDA and is now cleared to be prescribed so that it can be observed in a larger manor
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15
Q

Properties of a nursing assessment

A
  • this is the collection of baseline data in order to evaluate the therapeutic and adverse effects on a person, as well as the identification of high risk patients and the patient’s capacity for self care
  • the nurse must ask about drug history, surgery history, family history, etc. in order to assess how to treat the patient properly
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16
Q

Category A pregnancy drugs

A
  • Adequate and well-controlled studies have failed to demonstrate a risk to the fetus in the first trimester of pregnancy (and there is no evidence of risk in later trimesters)
17
Q

Category B pregnancy drugs

A
  • Animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in pregnant women.
18
Q

Category C pregnancy drugs

A
  • Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks.
19
Q

Category D pregnancy drugs

A
  • There is positive evidence of human fetal risk based on adverse reaction data from investigational or marketing experience or studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks.
20
Q

Category X pregnancy drugs

A
  • Studies in animals or humans have demonstrated fetal abnormalities and/or there is positive evidence of human fetal risk based on adverse reaction data from investigational or marketing experience, and the risks involved in use of the drug in pregnant women clearly outweigh potential benefits.
21
Q

Pure food and drug act (1906)

A
  • passed to protect the public from adulterated or mislabeled drugs
22
Q

Food drug and cosmetic act (1938)

A
  • mandated that drug manufacturers must test all drugs for harmful effects
  • mandated drug labels must be accurate and complete
23
Q

Kefauver - harris amendment (1962)

A
  • resulted from drug companies making huge profits and sometimes using false or misleading promotions (thalidomide)
24
Q

Controlled substances act (1970)

A
  • categorized controlled substances on the basis of their relative potential for abuse
25
Q

Drug regulation act (1978)

A
  • shortened the drug investigation process to release drugs sooner to the public
26
Q

Characteristics of Scheduled drugs

A
  • these are drugs that are to be taken at specific times
  • these drugs do not pass through your system for a certain span of time and are used to keep a constant effect on the body, like birth control. Because of this, these drugs are taken on schedules to keep up the effect of the drug.
27
Q

First Pass Effect

A
  • is a phenomenon of drug metabolism whereby the concentration of a drug is greatly reduced before it reaches the systemic circulation
  • drugs with first pass effects must be administered in much higher doses
28
Q

difference between side effects, adverse effects, allergic effects and ethnic differences of drugs

A
  • a side effect is when a drug interacts with something in your body causing a reaction
  • an allergic effect is when a drug reacts with your immune system
  • an adverse effect is an unwanted or unpleasant effect caused by a drug
  • ethnic differences are differences in drug metabolism in different ethnicities