Chapter 1 Flashcards

1
Q

Definition: Drug

A

Any chemical that can affect living processes.

Any chemical can be considered a drug at a high enough dose.

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2
Q

Definition: Pharmacology

A

The study of drugs and their interactions with living systems.

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3
Q

Definition: Clinical Pharmacology

A

The study of drugs in humans.

Used to develop therapeutics.

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4
Q

Definition: Therapeutics (Pharmacotherapeutics)

A

The use of drugs to diagnose, prevent, or treat disease or to prevent pregnancy.
Alternatively, the medical use of drugs.

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5
Q

Properties of an Ideal Drug

The Big Three

A

Effectiveness: The drug does what it is meant to.

Safety: The drug is not harmful. Some drugs will always cause harmful effects, such as chemotherapies. Drug selection and dosage needs to minimize potential harm.

Selectivity: The drug only does one thing. There is no such thing as an entirely selective drug.

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6
Q

Additional Properties of Ideal Drugs

Reversible Action

A

Effects are reversible and subside within an appropriate time.

Ex: Birth control does not cause sterility and people wake up after general anesthesia.

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7
Q

Additional Properties of Ideal Drugs

Predictability

A

The drug does the same thing to everyone.

This isn’t actually possible because every person responds uniquely. This is why drug treatments must be tailored to each individual.

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8
Q

Additional Properties of Ideal Drugs

Ease of Administration

A

The route of administration should be convenient and the doses per day should be low.

Ease of administration increases patient adherence and decreases risk.

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9
Q

Additional Properties of Ideal Drugs

Freedom from Drug Interactions

A

Almost all drugs have interaction with other drugs. Interactions need to be considered when choosing drug therapies. Ideal drugs would have no interactions.

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10
Q

Additional Properties of Ideal Drugs

Low Cost

A

Ideal drugs are easy to afford. People won’t take drugs they can’t afford.

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11
Q

Additional Properties of Ideal Drugs

Chemical Stabilty

A

The drug does not lose effectiveness during storage.

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12
Q

Additional Properties of Ideal Drugs

Possession of a Simple Generic Name

A

Nobody has time for complex names. When patients don’t remember the names of their drugs it can lead to inaccurate histories.

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13
Q

Definition: The Therapeutic Objective

A

To provide maximum benefit with minimal harm.

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14
Q

Four factors that determine the intensity of the drug response

A
  1. administration
  2. pharmacokinetics - body’s impact on the drug
  3. pharmacodynamics - impact of drugs on the body
  4. individual variations

remember: kinetics – how the body moves the drug

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15
Q

Five rights of medication safety

A
right drug
right patient
right dose
right route
right time
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16
Q

What’s the difference between an RN and a med tech

A

RN exercises judgment/clinical reasoning

17
Q

FDA purpose

A

protect public: safety, effectiveness, post-marketing surveillance

18
Q

Four stages of drug approval

A
  • preclinical investigation
  • clinical investigation
  • FDA review
  • postmarketing surveillance
19
Q

Three phases of clinical trials

A
  • healthy (20-80)
  • pts. with disease (100-300)
  • pts in hospitals and clinics, incl complex health conditions (1000-3000)

don’t need to know numbers, just know that it’s more and more

20
Q

Does schedule I or schedule V have a higher potential for abuse?

A

schedule I is higher potential for abuse

21
Q

therapeutic vs pharmacological

A

therapeutic – why to use it e.g. antihypertensive

pharmacological – mechanism of action e.g. antidiuretic, beta blocker

22
Q

differences between brand name and generic meds

A

bioavailability, cost, formulations (inert substances)

23
Q

Are generic and brand name meds the same?

A

They have the same active ingredient, but differences in inert substances may affect bioavailability