Pharmacology, Drug Class, and Body Systems Flashcards

(43 cards)

1
Q

The study of the movement of drugs through the body

A

Pharmacokinetics (Absorption, Distribution, Metabolism, Excretion)

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2
Q

The study of the effects of drugs’ actions on

A

Pharmacodynamics

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3
Q

Terms that are named for the person who discovered the illness or procedure?

A

Eponyms

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4
Q

Error-prone abbreviation

A

U, ug, QD, Hs, QOD, SC or SQ

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5
Q

Error-prone symbols

A

Trailing zeros and naked decimals

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6
Q

Trailing zeros

A

Medication written as 5.0 mg can be easily misinterpreted as 50 mg.

The recommendation, in this case, is to write the medication dose as 5 mg.

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7
Q

Naked decimals

A

Medication written as .5 mg can be easily misinterpreted as 5 mg if the decimal is unclear.

Instead, the dose should be written as 0.5 mg.

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8
Q

Drug Nomenclature

A

Chemical name, generic name, brand name.

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9
Q

The FDA defines drugs as these items:

A

. A substance recognized by an official
pharmacopeia or formulary
. A substance intended for use in the
diagnosis, cure, mitigation, treatment, or
prevention of disease
. A substance (other than food) intended
to affect the structure or any function of
the body

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10
Q

Chemical Name

A

Long scientific name that represents a drug’s
molecular structure.

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11
Q

Generic Name

A

Nonproprietary name of the drug that isn’t
protected by patent or trademark.

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12
Q

Brand Name

A

Name given by a manufacturer that holds
proprietary ownership, or patent, of the drug.

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13
Q

Dosage Forms

A

Oral, parenteral, Topical, other

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14
Q

Therapeutic Equivalence

A

when two drugs have the same clinical effect.

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15
Q

Bioequivalent

A

both drugs are equally effective and safe, and are equally absorbed when taken in the body.

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16
Q

The Orange Book

A

The FDA keeps a list of all therapeutic equivalents in a book called the Orange Book.

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17
Q

Pharmaceutical Alternatives

A

they have the same active ingredient, but are different strengths or dosage forms.

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18
Q

Therapeutic Interchange

A

occurs when a patient’s drug is substituted with a drug that has a different chemical makeup but the same result.

19
Q

Before prescribing drugs, a physician must know which of
the following aspects that relate to the medicine?

A

What will the drug do to the body?
Will the drug have any side effects?
What will the body do with the drug?
How much of the drug is required by the body?

20
Q

Pharmaceutics

A

The specific dosage form of a medication is designed to achieve
maximum benefit and to avoid side effects.

21
Q

Therapeutics

A

Drugs have effects,
which lead to treatment
of disease.

22
Q

Bioavailability

A

Only a portion of the drug
enters the bloodstream and
affects the body.

23
Q

Passive Diffusion

A

Movement of drug molecules from an area of high
concentration of the drug to an area of low concentration
Doesn’t require energy
Example: Respiratory gases like oxygen

24
Q

Facilitated Diffusion

A

Uses special carrier protein molecules to move drugs
across the membrane
Does not require energy
Example: Glucose

25
Active Transport
Requires energy or ATP to move drug molecules across cell membrane Movement occurs in one direction Can move from lower concentration to higher Less common method Example: Sodium/potassium pump needed to transport amino acids, sugars, and lipids.
26
Bulk Transport
Phagocytosis ("Cell eating") Pinocytosis ("Cell drinking")
27
Phagocytosis ("Cell eating")
Cell membrane physically engulfing the drug molecule Example: White blood cell engulfing an invading bacterium
28
Pinocytosis ("Cell drinking")
Drug molecules are surrounded and brought into the cell. Example: Vitamin B12 in the GI tract
29
Metabolism
Enzymes alter drugs in the liver (biotransformation) Preapares drug for excretion
30
Excretion
Excretion is a process by which drugs are removed from the body. The process of drug removal is also known as elimination. This is the final step in pharmacokinetics. Most elimination occurs in the kidneys and into the urine. Clearance is the rate at which drugs leave the body. Clearance is varied and is measured by half-life elimination.
31
Half-Life Elimination:
Term used to describe how long it takes for the drug concentration to decrease by 50%.
32
Distribution
impacted by blood flow to the affected area, cell membrane permeability, and the chemical properties of drugs.
33
Agonist Chemicals
A chemical that binds to the receptor and elicits an appropriate response
34
Antagonist Chemicals
A chemical that binds to the receptor but elicits no response and blocks access to the receptor by an agonist
35
Therapeutic Effects
Intended effect: Local Effects Decreasing inflammation at site of injury Treating itchiness Systemic Effects Reducing fever Lowering cholesterol Reducing blood pressure
36
Therapeutic window (therapeutic index)
The range between the specific drug concentration needed to produce a desirable therapeutic effect and the concentration that will cause toxicity
37
Adverse Effects
Negative effects of a drug: These may occur even when taken as prescribed at normal therapeutic dosages. Nausea Vomiting Headache Aches and pains Toxicity: Toxicity may also cause side effects.
38
Toxicity:
Harmful effect of a drug that occurs when plasma concentration is higher than the recommended therapeutic level.
39
Factors Affecting Drug Actions
Types of Effects Patient demographics Genetic factors Associated diseases Psychological factors Route of administration Patient compliance (example: taking all doses as prescribed) Environmental factors
40
Drug Interactions
is the result of a drug being taken with another substance that may change the drug's intended effects. (Synergistic, Antagonistic)
41
Synergistic
When a drug and another substance are taken together, the combined effect is greater than the effect of each taken separately.
42
Antagonistic
When a drug and another substance are taken together, the combined effect is less than the effect of each taken separately. The two substances interfere with each other.
43