Basic Pharmacology Flashcards

1
Q

The science that deals with the study of drugs in all its aspects.

A

Pharmacology

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2
Q

The study of the drug in terms of its history, source of chemical and physical properties, mechanism of action, absorption, distribution, bio-transformations and other uses of the drug.

A

Pharmacology

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3
Q

The study of the way a drug is ABSORBED, then DISTRIBUTED to the tissues of the body, METABOLIZED and EXCRETED.
MOVEMENT of the drug in the body

A

Pharmacokinetics

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4
Q
  • The study of a DRUG’s ACTIVITY, describing the nature and magnitude of the response, once it reaches its SITE OF ACTION.
  • What the drug DOES to a body
A

Pharmacodynamics

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5
Q

Determines the DOSAGE of the drug recommended for patients, and HOW they should TAKE it.

A

Pharmacokinetic Profile

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6
Q

What are the 4 Pharmacokinetic Processes?

A

Absorption
Digestion
Metabolism
Excretion

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7
Q

The process by which a drug moves from the SITE OF ADMINISTRATION into the BLOODSTREAM.

A

Absorption

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8
Q

The process by which a drug, when taken, is PARTITIONED among THE VARIOUS ORGANS and TISSUES in the body where the drug EXERTS ITS ACTION.

A

Distribution

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9
Q

The process by which a drug in the body may be changed into other, usually smaller, molecules called METABOLITES.

A

Metabolism

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10
Q

The process by which drugs or their metabolites are eliminated from the body

A

Excretion

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11
Q

Rate of absorption affects _______ and ______.

A

Duration

Intensity of Action

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12
Q

Factors affecting absorption are:

A
Gastric Motility
Rate of Blood Flow
Area of Absorbing Surface
Molecular Size
Solubility

GRAMS

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13
Q

Body compartments in which drugs accumulate

A

Reservoir

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14
Q

Also known as biotransformation

A

Metabolism

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15
Q

True or False.

Metabolites may be active or inactive, usually lees active than the parent drug

A

True

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16
Q

Metabolism happens in the _____, if drug is taken orally.

A

Liver

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17
Q

True or False.

Lipid Soluble drugs are eliminated faster

A

False. They are eliminated slowly

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18
Q

True or False.

Drugs are eliminated in the body either unchanged or as metabolites

19
Q

What are the 7 excretory Routes.

A
Sweat
Tears
Respiratory Gases
Saliva
Mother's Milk
Urine
Stool
20
Q

What are the 6 Pharmacokinetic Parameters?

A
Bioavailability
Area under the curve
Peak serum concentration
Half life
First-pass effect
Blood protein binding
21
Q

The amount of the ADMINISTERED drug which arrives in its THERAPEUTIC form at the SITE OF ACTION

A

Bioavailability

22
Q

Measurement of the AMOUNT of drug that has been ABSORBED at a GIVEN TIME after administration

A

Area under the Curve

23
Q

The MAXIMUM level of drug achieved in the BLOODSTREAM

A

Peak serum drug concentration

24
Q

The TIME it takes for the concentration of the drug in the bloodstream to fall to half of its peak value.

25
The metabolism of drugs the FIRST TIME they pass through the LIVER, before they have the chance to circulate to other body tissues. May reduce bioavailability and so affect dosage.
First-Pass Effect
26
The affinity of a drug to bind with proteins, chiefly ALBUMIN, in the blood stream
Blood Protein Binding
27
True of false. Protein bound proportion of a drug may be pharmacologically inactive, leaving only the unbound drug being available to the tissues.
True
28
What are the two pharmacodynamic parameters?
MIC - minimum inhibitory concentration | MBC - minimum bactericidal concentration
29
Lowest drug concentration needed to inhibit the growth of the bacteria
Minimum Inhibitory Concentration
30
Lowest drug concentration needed to kill a particular bacteria strain
Minimum Bactericidal Concentration
31
Length of time that the serum concentrations of the antibiotic remains higher than the MIC.
T>MIC | Time above MIC
32
3 Pharmacodynamic Properties
Drug Action Drug Effects Drug Response Curves
33
The initial INTERACTION of the drug with its receptor/target molecule
Drug Action
34
Physiological Effects that result from the binding of the drug with its receptor.
Drug Effects
35
Efficacy of the drug at different DOSES.
Drug Response Curves
36
Used to designate a quantitative statement of the selectivity of the drug when a therapeutic and an untoward effect are being compared.
Therapeutic Index TD50 ____ ED50
37
Has therapeutic effects at a dose that is unlikely to cause toxic effects
Wide therapeutic index
38
Has therapeutic effects at a dose that is close to the toxic dose
Narrow therapeutic Index
39
Unwanted effects that occur when the drug is used within its normal dosage range
Side Effect
40
Potentially dangerous effect that occur at doses higher than the normal therapeutic range
Toxic effect
41
The ability to cause developmental defects in the fetus
Teratogenicity
42
The ability to cause toxic effects in the fetus
Fetotoxicity
43
Patient Factors Influencing Risk of Adverse Reactions
``` Body Weight Age and Sex Allergy Route of Administration Time of Administration ```
44
The science and art of using drugs in the treatment of disease
Pharmacotherapeutics