Terminologies in Introduction to Pharmacology Flashcards

1
Q

Defined as any chemical that can affect living processes.

A

Drug

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2
Q

The study of drugs and their interactions with living systems.

A

Pharmacology

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3
Q

The use of drugs to diagnose, prevent, or treat disease or
to prevent pregnancy. Can also be defined
simply as the medical use of drugs

A

Pharmacotherapeutics

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4
Q

Defined as the study of drugs in
humans. This discipline includes the study of drugs in patients
as well as in healthy volunteers (during new drug development).

A

Clinical Pharmacology

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5
Q

Properties of an ideal drug

A

-Effectiveness
-Safety
-Selectivity
-Reversible Action
-Predictability
-Ease of Administration

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6
Q

What is the objective of drug therapy?

A

Is to provide maximum
benefit with minimum harm

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7
Q

10 Right’s of Medication

A

Right Patient
Right Route
Right Time
Right Drug
Right Dosage
Right Documentation
Right Education
Right Assessment
Right to Refuse
Right Evaluation

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8
Q

Describe the drug’s chemical structure (acetaminophen, dexbrompheniramine maleate tablet)

A

Drugs Chemical Name

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9
Q

It’s the official, non-proprietary, chosen by the drug company and registered as trademark. (Paracetamol)

A

Drugs Generic Name

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10
Q

Proprietary name, chosen by the drug company and registered as trademark (Biogesic)

A

Trade/Brand Name

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11
Q

Process determine how much of an administered dose gets to its sites of action. Derived from two Greek words:
pharmakon means drug or poison and kinesis means motion.

A

Pharmacokinetics

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12
Q

Pharmacokinetics 4 processes:

A

Absorption
Distribution
Metabolism/Biotransformation
Excretion

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13
Q

Drug’s that may purchased without direct prescription

A

Over the counter drugs

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14
Q

Stands for pro re nata, a Latin phrase meaning as needed

A

PRN

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15
Q

What is your role as a nurse when you’re giving a information about:

  • Drug name and therapeutic category (e.g., penicillin: antibiotic)
  • Dosage
  • Dosing schedule
  • Route and technique of administration
  • Expected therapeutic response and when it should develop
  • Nondrug measures to enhance therapeutic responses
  • Duration of treatment
  • Method of drug storage
  • Symptoms of major adverse effects, and measures to minimize discomfort and harm
  • Major adverse drug-drug and drug-food interactions
  • Whom to contact in the event of therapeutic failure,
    severe adverse reactions, or severe adverse interactions
A

Nurse as a Educator

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16
Q

Also known as compliance or concordance that can
be defined as the extent to which a patient’s behavior coincides with medical advice.

A

Patient Adherence

17
Q

Clinical trials occur in four phases and may take 2 to 10 years
to complete. The first three phases are done before a new drug
is marketed. The fourth is done following FDA approval for
marketing.

A

Clinical Testing

18
Q

Route of administration via GI tract

A

Enteral

19
Q

Route of administration outside the GI tract

A

Parenteral

20
Q

Refers to the rapid inactivation of some oral drugs as they pass through the liver after being absorbed

A

First-pass effect

21
Q

Defined as the plasma drug level below which therapeutic effects will not occur.

A

Minimum Effective Concentration (MEC)

22
Q

The time required for the amount of drug in the body to decline by 50%.

A

Half-life

23
Q

Defined as the study of the biochemical and physiologic effects of drugs on the body and the molecular mechanisms by which those effects are produced

A

Pharmacodynamics

24
Q

Any functional macromolecule in a cell to which a drug binds to produce its effects.

A

Receptor

25
Q
  • Drugs that can mimic the action of endogenous compounds.
  • Drugs that can block the action of normal receptor activity regulated by endogenous compounds.
    -Limited affinity to receptors site
A

-Agonist
-Antagonist
-Partial Agonist